Pathological Conditions, Anatomical

Caduta nella voragine

Barabino A.

2026/3 — pag. 158-160 — DOI

Porpora di Schönlein-Henoch bollosa Mononucleosi

2025/10 — pag. 668 — DOI

Volvolo da malrotazione intestinale in un lattante: una sfida diagnostica

Ferrari M, Perre E, Lombardo VF, Di Florio F, Ghizzi C

2025/9 — pag. 251-252 — DOI

A 1-year-old boy presenting with irritability, lethargy and vomiting was diagnosed with small bowel volvulus due to intestinal malrotation. Prompt surgical intervention prevented severe complications. The case highlights the importance of considering...

Quando l’anamnesi non aiuta... occhio alla clinica (e alla milza)

Sardella L, Abbagnato L, Agosti M, Salvatore S, Selicorni A.

2025/8 — pag. 530 — DOI

The case of a 15-year-old girl with Epstein-Barr virus infectious mononucleosis complicated by splenomegaly and traumatic splenic rupture with haemoperitoneum is described. She was treated with splenic embolization, blood transfusion, antibiotic ther...

Galeotto fu il parvovirus

Vecchi M, Cavalleri L

2025/8 — pag. 215-216 — DOI

A previously healthy 2.5-year-old child presented in critical condition with hypoglycemic coma, severe metabolic acidosis and profound anaemia. Diagnostic work-up revealed previously undiagnosed sickle cell disease (SCD) complicated by aplastic crisi...

Sclerosi epatoportale

Sparaventi C, Zago A, Di Leo G, Barbi E, Bramuzzo M.

2025/7 — pag. 453-455 — DOI

Hepatoportal sclerosis is a rare and underdiagnosed liver condition characterised by histological alterations of the portal venules and hepatic sinusoids, with periportal fibrosis and vascular narrowing. Its diagnosis is histological and requires liv...

I disturbi respiratori ostruttivi del sonno

Basilicata S, Traunero A, Borrelli M, Maschio M, Ghirardo S, Amaddeo A.

2025/6 — pag. 359-365 — DOI

Obstructive sleep disordered breathing encompasses different clinical entities, the most severe of which is obstructive sleep apnea syndrome (OSAS). Children with severe adenotonsillar hypertrophy, obesity, congenital malformations or specific syndro...

Tiroidite acuta... ma non troppo

Proietti Gaffi G, Naim A, Baldioli E, Spacco G, Gastaldi R, Napoli F, Maghnie M

2025/6 — pag. 160-161 — DOI

The paper reports the case of a 7-year-old girl with recurrent suppurative thyroiditis, associated with a fourth branchial arch cyst and pyriform sinus fistula. After several episodes initially treated with corticosteroids, the diagnosis was confirme...

Associazione VATER/VACTERL

Scupilliti S, Vancini A, Selicorni A

2025/5 — pag. 317-319 — DOI

Bambino immobile: pensa anche alla miocardite

Rivellino L.

2025/4 — pag. 253-256 — DOI

This report describes a case of acute myocarditis in a 2-year-old child. Acute myocarditis is most commonly secondary to viral infections and, less frequently, to immune disorders or drug reactions. Among the various viruses, parvovirus B19 is rec...

Desametasone nella meningite batterica Celiachia ai tempi dell’AI Torsione ovarica, sempre in guardia Diarree intrattabili 2025 sul NEJM Acalasia POE(M)-SIA? Skin of Colour

2025/4 — pag. 217-218 — DOI

Tachiaritmia sopraventricolare in un neonato nato a 32 settimane di età gestazionale

Valencic I, Bronzetti G, Vitali F, Corvaglia L

2025/4 — pag. 86-92 — DOI

Tachyarrhythmias affect 1-5% of neonates and result from an abnormal conduction of the depolarization wave, which in 80% of cases manifests as paroxysmal supraventricular tachycardia (PSVT). These arrhythmias are generally well tolerated but sometime...

Leishmania e linfoistiocitosi emofagocitica (HLH)

Bratta A, Arcuri L, Micalizzi C

2025/2 — pag. 51-52 — DOI

Haemophagocytic lymphohistiocytosis (HLH) is a rare life-threatening hyperinflammatory syndrome. The paper reports the case of a 5-month-old infant hospitalised with persistent fever, splenomegaly and significant inflammatory activation. After an ini...

Emangioma congenito in sindrome PHACE, esiste una correlazione?

Carzaniga V, Pangallo E.

2025/1 — pag. 48-49 — DOI

A newborn with facial haemangiomas and vascular malformations, including an arteriovenous fistula, is diagnosed with PHACE syndrome. At the age of 4 months, following the worsening of her malformations, she undergoes endovascular embolization. Follow...

Colecistite acuta da EBV

Favaretto E

2025/1 — pag. 21-22 — DOI

The paper describes a rare instance of acute acalculous cholecystitis (ACC) in a 7-year-old boy caused by Epstein-Barr virus (EBV) infection. Initially, he was suspected to have appendicitis, but subsequently imaging and laboratory tests revealed ACC...

Una diagnosi precoce di coartazione aortica e sindrome di Williams

Mazza S, Corona L, Atzei A, Fanos V, Paola Neroni P

2024/10 — pag. 217-218 — DOI

A newborn diagnosed with severe aortic coarctation underwent surgical repair but developed re-coarctation and pulmonary artery narrowing. Persistent eyelid oedema and dysmorphic features led to a suspicion of Williams Syndrome, confirmed through gene...

Rivista sfogliabile on line

2024/7

"Deep purple": un caso di purpura fulminans in asplenia congenita isolata

Cattaneo F, Mariani E, Lazzerotti A

2024/7 — pag. 468-470 — DOI

Asplenic patients are well-known to be at higher risk of infections, which are primarily caused by Streptococcus pneumoniae. Such infections may present with a sudden onset and a fulminant course, potentially leading to septic shock, purpura fulminan...

Calcolosi renale e infezione delle vie urinarie

Cangemi F, Aloisio A, D’Alessandro MM, Corsello G.

2024/7 — pag. 465-466 — DOI

This case highlights the importance of investigating persistent leukocyturia, as it may indicate nephrolithiasis and require early treatment....

La calcolosi renale come causa di dolore addominale

Burlo F.

2024/7 — pag. 465-466 — DOI

This case shows that kidney stones can cause atypical pain and that large stones require surgical intervention. It has also highlighted how impressions about patients can influence the diagnosis....

La torsione dell'ovaio può essere subdola

Tonetto S.

2024/5 — pag. 332-334 — DOI

The case of a 13-year-old girl presenting with abdominal pain and vomiting, ultimately diagnosed with ovarian torsion, is described...

L’ittero in un lattante

Moras M, Tanzi G, Melli P, Cogo P.

2024/5 — pag. 329-331 — DOI

The diagnosis of biliary atresia was ultimately made in an infant who still presented with jaundice after his first month of life and had previously been misdiagnosed with breast milk jaundice. The authors underline that biliary atresia should always...

La torsione dell'ovaio può essere subdola

Tonetto S

2024/5 — pag. 87-87 — DOI

The case of a 13-year-old girl presenting with abdominal pain and vomiting, ultimately diagnosed with ovarian torsion, is described...

Ipospadia

Vrinceanu AM, Barbi E, Scarpa M-G, Olenik D, Iaquinto M

2024/4 — pag. 227-231 — DOI

The paper reports a clinical case of a boy who underwent surgery for proximal hypospadia and developed postoperative complications. Furthermore, the current knowledge on hypospadias, addressed to paediatricians and other non-surgical professionals is...

Lattante con inappetenza in Pronto Soccorso: una sfida per il pediatra

Leotta M, Cavallaro P, De Santis A, Cioffi S, Della Vecchia N, Papini L, Cristaldi S, Musolino AM, Pisani M, Raucci U, Villani A.

2024/2 — pag. 123-126 — DOI

The Authors describe the case of a 2-month-old inappetent infant finally diagnosed with a left diaphragmatic hernia....

Lattante con inappetenza in Pronto Soccorso: una sfida per il pediatra

Leotta M, Cavallaro P, De Santis A, Cioffi S, Della Vecchia N, Papini L, Cristaldi S, Musolino AM, Pisani M, Raucci U, Villani A

2024/2 — pag. 33-34 — DOI

The authors describe the case of a 2-month-old inappetent infant finally diagnosed with a left diaphragmatic hernia....

Un bersaglio quando meno te lo aspetti: la sindrome di Peutz-Jeghers

Neirotti A, Rossi L, Parola F, Scarcia S, Brach del Prever AM.

2024/1 — pag. 54-57 — DOI

Peutz-Jeghers Syndrome is a genetic condition that puts affected patients at risk of oncological degeneration and gastrointestinal complications. In most cases, abdominal pain is the acute symptom that leads the patient to the emergency room. This ma...

Sferocitosi: una famiglia... tre malattie!

Ferrara D, Giordano C, Borsellino Z, Cuccia L, Ruffo GB, Corsello G.

2024/1 — pag. 54-57 — DOI

The paper describes the cases of three siblings affected by Hereditary Spherocytosis (HS). The different clinical presentations in the same family are examples of the heterogeneity of this pathology. HS is a common inherited type of haemolytic anaemi...

Quando pensare alla splenectomia in presenza di Beta-talassemia con drepanocitosi?

Stera G, Legnani E, Grasso A

2024/1 — pag. 21-21 — DOI

The authors describe the positive effect of splenectomy in two brothers affected by micro-drepanocytosis....

Volvolo prenatale: gestione clinica dall’isola neonatale alla sala operatoria

Franzone D, Data E, Lionetti B, Pellegrino M, Avanzini S, Allodi A

2024/1 — pag. 15-16 — DOI

Intestinal obstructions are one of the most common reasons for surgery in newborns. The most common causes are anorectal malformations, small intestine atresia and Hirschsprung’s disease. Such conditions may present unexpectedly and may require urge...

Sferocitosi: una famiglia... tre malattie!

Ferrara D, Giordano C, Borsellino Z, Cuccia L, Ruffo GB, Corsello G

2024/1 — pag. 5-8 — DOI

The paper describes the cases of three siblings affected by Hereditary Spherocytosis (HS). The different clinical presentations in the same family are examples of the heterogeneity of this pathology. HS is a common inherited type of haemolytic anaemi...

Un bersaglio quando meno te lo aspetti: la sindrome di Peutz-Jeghers

Neirotti A, Rossi L, Parola F, Scarcia S, Brach del Prever AM

2024/1 — pag. 1-4 — DOI

Peutz-Jeghers Syndrome is a genetic condition that puts affected patients at risk of oncological degeneration and gastrointestinal complications. In most cases, abdominal pain is the acute symptom that leads the patient to the emergency room. This ma...

Lesioni perianali

Burlo F, Ballaben A, Bramuzzo M, Lega S.

2023/10 — pag. 647-652 — DOI

Anorectal diseases are quite common in children, but their management often raises uncertainty. The most frequent lesions are anal fissures, which are mainly linked to constipation. Intense strain may also lead to rectal prolapse or haemorrhoids. Per...

Timo ectopico: quando pensarci, la diagnosi per immagini, la gestione

Bisi R, Troisi A, Wrona D, Marchetti F, Parenti G

2023/10 — pag. 631-636 — DOI

Ectopic thymic tissue is a rare occurrence in clinical practice. However, it could cause diagnostic difficulties, especially in the paediatric age group, as it can mimic a cervical mass. In most cases, thymic ectopia is asymptomatic and the ectopic t...

Spettro oculo-auricolo-vertebrale

Carrer A, Mariani M, Selicorni A

2023/8 — pag. 521-522 — DOI

Ipertrofia tonsillare asimmetrica Diabete: time in range

2023/5 — pag. 335 — DOI

Una cisti troppo repentina

Buschini MP.

2023/5 — pag. 326-328 — DOI

The incredible story of a candy mistaken for a cyst is described....

Lesioni da “capello attorcigliato” in un lattante

Mincuzzi G, Alessi M, Spataro A, Corsello G.

2023/5 — pag. 319-320 — DOI

Hair thread tourniquet syndrome is a paediatric condition due to a hair or cotton thread from infants' clothes that gets tangled around the extremities of the body, tightening the skin until it causes a clean cut. The injury could develop into ischem...

Calcolosi delle vie urinarie

2023/4 — pag. 265 — DOI

Fibromatosis colli: due casi clinici

Colombo M, Pacenza M, Argentieri A.

2023/3 — pag. 189-191 — DOI

Fibromatosis colli is a rare cause that should not be forgotten, especially for the morbidity that can arise in the case of diagnostic delay (torticollis and facial asymmetries). An adequate medical history and a good physical examination can lead to...

Fibromatosis colli: due casi clinici

Colombo M, Pacenza M, Argentieri A

2023/3 — pag. 46-48 — DOI

Fibromatosis colli is a rare cause that should not be forgotten, especially for the morbidity that can arise in the case of diagnostic delay (torticollis and facial asymmetries). An adequate medical history and a good physical examination can lead to...

Il dolore alla schiena in un adolescente

Bontempo C, Lama C, Mambelli L, Feletti F, Lotta C, Marchetti F.

2023/2 — pag. 116-118 — DOI

Quando la tumefazione laterocervicale è una cisti branchiale

Gamba S

2023/2 — pag. 40-40 — DOI

The author describes the case of a 10-year-old boy presenting with a lateral cervical swelling. A branchial cyst was finally diagnosed....

Le bolle che non ti aspetti: un raro caso di pemfigo volgare in età pediatrica

Benelli E, Demarin GC, Corneli P, Gatti A, Martelossi S

2023/2 — pag. 21-24 — DOI

A healthy 15-year-old boy in full well-being presents with multiple ulcerative lesions with an erosive appearance at the level of the oral cavity and the nasal mucosa. Two months after the onset, vesicular lesions also appear on the skin. As pemphigu...

Acondroplasia

Calderara ML, Selicorni A.

2023/1 — pag. 49-51 — DOI

Rene singolo congenito

Gruppo di lavoro sulle malformazioni congenite dei reni e delle vie urinarie della SINePe

2023/1 — pag. 21-30 — DOI

In recent years, several studies have been published on the prognosis of children with congenital solitary kidney (CSK), but a worldwide consensus on management and follow-up is still lacking. Recently, the Italian Society of Pediatric Nephrology has...

Un Meckel fantasma

Malni I

2023/1 — pag. 11-12 — DOI

The case of a 3-year-old child with acute abdomen due to the perforation of a Meckel’s diverticulum is presented. At the first surgical exploration the diagnosis was misunderstood because of the anomalous positioning in the mesenteric side of the div...

Una cefalea con fremito

Trombetta A.

2022/10 — pag. 654-656 — DOI

A diagnosis of arteriovenous fistula was finally made in a 17-year-old girl presenting with “quivering” headache. A history of neonatal scalp catheterization was present....

Mangia come un uccellino...

Giuseppin I

2022/10 — pag. 652-653 — DOI

The diagnosis of Bochdalek hernia (left diaphragmatic hernia) was eventually made in a 17-month-old malnourished child presenting with fever, persistent vomiting and shortness of breath. The clinical and diagnostic implications of the diaphragmatic h...

Chiudete quella porta! Una rara causa di difficoltà di alimentazione del neonato

Gerosa GM, Orlandi S, Migliazza L, Mangili G, Cheli M

2022/10 — pag. 213-213 — DOI

Una cefalea con fremito

Trombetta A

2022/10 — pag. 209-209 — DOI

A diagnosis of arteriovenous fistula was finally made in a 17-year-old girl presenting with “quivering” headache. A history of neonatal scalp catheterization was present....

Un diverticolo (dav)vero sanguinante

Tessitore A

2022/8 — pag. 527-530 — DOI

Meckel diverticulum has been suspected and then diagnosed at laparoscopic exploration of the abdomen in a severely anaemic 16-month-old child with acute intestinal bleeding. The surgical indication of all unexplained intestinal bleedings is discussed...

Un diverticolo (dav)vero sanguinante

Tessitore A

2022/8 — pag. 174-175 — DOI

Meckel diverticulum has been suspected and then diagnosed at laparoscopic exploration of the abdomen in a severely anaemic 16-month-old child with acute intestinal bleeding. The surgical indication of all unexplained intestinal bleedings is discussed...

La calcolosi delle vie urinarie in età pediatrica a tutto tondo

Faraguna MC, Terranova CM, Peccatori N, Gnech M, Berrettini A, Melzi ML.

2022/7 — pag. 435-440 — DOI

Overall, the incidence of paediatric urolithiasis is increasing; 50-90% of cases are due to metabolic alterations, 3-30% are associated with urinary tract infections and the remaining cases are idiopathic. About 20-30% of children, especially boys wh...

Ernia diaframmatica a presentazione tardiva

Botusan RA, Zarrilli S, Gallo MG, Santillo V.

2022/6 — pag. 378-380 — DOI

Una ematemesi fatale

Amoroso A, Di Stasio F, Locatelli L, D’Antiga L

2022/4 — pag. 81-85 — DOI

Disk battery ingestions in children are increasing worldwide. This condition may cause severe complications, especially if the battery is lodged in the oesophagus. The most dangerous complication with the highest mortality rate is aorto-oesophageal f...

Il tifo

Palladino F, Coppola C, Prisco A, Puzone S, Imperatore A, Brienza C, Nunziata F

2022/3 — pag. 68-70 — DOI

The paper describes the case of a 13-year-old boy presenting with fever with chills, abdominal pain and diarrhoea. Further investigation showed an “enteric fever”. Finally, clinical onset, diagnosis and disease management are discussed. ...

Noduli di Bohn Nevo sebaceo

2022/2 — pag. 132

Quando la linfoistiocitosi emofagocitica è secondaria

Ventresca S, Fabbri E, Bracaglia C, Gasperini P, Filippini B, Libertucci F, Bigucci B, Pericoli R, Vergine G.

2022/2 — pag. 97-102 — DOI

The paper describes the case of a 1-year-old Caucasian boy with a 1-month history of fever and splenomegaly. Laboratory findings showed pancytopenia, hypertriglyceridemia and hyperferritinemia. Secondary haemophagocytic lymphohistiocytosis was suspec...

Le onicoeterotopie in età pediatrica

Ferrari M, Mazzarello V, Barbi E

2021/9 — pag. 283-284 — DOI

The ectopic nail is an additional nail located in an abnormal site. It falls within onychoheterotopia that is a rare condition whose pathogenesis is indeterminate. Ectopic nails are distinguished from the double little toenail by aetiology, location ...

Quando non trascurare la splenomegalia nel lattante

Zama D, Parladori R, Muratore E, Melchionda F, Baronio F, Pession A

2021/8 — pag. 501-507 — DOI

Splenomegaly in children is really common and its main cause is infectious disease. The aetiology in newborns and older children is well established, while it is less defined in suckling infants. The paper describes three cases of splenomegaly in inf...

Covid-19: pistole e orfani Per una volta parliamo dei (vasi) linfatici Sarcopenia e MICI Cose del genere Quando San Cortisone perde le staffe

2021/7 — pag. 417-418 — DOI

La malrotazione intestinale: cosa deve sapere il pediatra

Tumminelli C, Galimberti AMC, Di Leo G, Codrich D, Murru FM, Gortani G

2021/3 — pag. 196-199 — DOI

Intestinal malrotation includes anomalies of intestinal rotation and fixation occurred during em-bryogenesis. It may present with acute or chronic-intermittent symptoms or remain asymptomatic. There are several methods to identify a defect of intesti...

La malrotazione intestinale: cosa deve sapere il pediatra

Tumminelli C, Galimberti AMC, Di Leo G, Codrich D, Murru FM, Gortani G

2021/3 — pag. 78-83 — DOI

Intestinal malrotation includes anomalies of intestinal rotation and fixation occurred during embryogenesis. It may present with acute or chronic-intermittent symptoms or remain asymptomatic. There are several methods to identify a defect of intestin...

La cisti sierosa parauretrale in una neonata

Marinelli I

2021/1 — pag. 53-54 — DOI

Paraurethral or Skene’s duct cysts are a rare congenital abnormality in the female neonate and are characterised by a round, yellow or orange-coloured cystic mass on either side of the urethra meatus. Excision, marsupialization and needle aspiration ...

Coscienza fluttuante, intestino sofferente

Agrusti A, Pederiva F, Cerrina A, Murru FM, Conte M

2021/1 — pag. 19-21 — DOI

Altered state of consciousness in infants can be the sole sign of a compromised intestinal blood flow. The article reports the case of an infant with inconsolable crying and lethargy with an omphalomesenteric duct remnant causing small bowel volvulus...

Diagnostica dell’allergia alimentare Lussazione dell’anca, eterometria degli arti inferiori Vaccino antipertosse e anafilassi

2020/8 — pag. 539 — DOI

Un prolasso nell’ambulatorio... “sbagliato”

A. Daidone

2020/7 — pag. 461-463 — DOI

La diagnosi e la gestione del prolasso rettale

S. Ventresca, M. Bacchini, G. Graziani, F. Marchetti

2020/7 — pag. 453-457 — DOI

Rectal prolapse is an overall rare occurrence in children in the first 4 years of age. It typically tends to relapse. In the majority of cases it is not possible to highlight a single cause that determines prolapse, even if it is more frequent in chi...

Un mal di pancia capriccioso

C. Corrado

2020/6 — pag. 141-141 — DOI

Il bambino con eccesso di crescita tra variabilità clinica ed eterogeneità genetica

G. Serra, M. Schierz, V. Antona, C.F. Giardina, M. Giuffrè, E. Piro, G. Corsello

2020/4 — pag. 243-248

Either in the newborn or in the child overgrowth can be generalized or localized if it is limited to one or more body regions. When overgrowth depends on a metabolic imbalance, or it is constitutional, the excessive growth can be the only clinical si...

Un’otorrea infinita

F. Forte, D. Cifarelli, P. Appio, M. Delvecchio, A. Derosa, C. Di Lucca, T. Faillace, C. Figliuolo, V. Targiani, R. Davanzo

2020/3 — pag. 188-190

Branchial arch anomalies (sinuses, fistulae, cysts and condral remnants) represent one of the commonest paediatric neck malformations. The paper describes a case study of a 2-year-old girl who presented with a persistent left-sided ear drainage, unre...

Un’otorrea infinita

F. Forte, D. Cifarelli, P. Appio, M. Delvecchio, A. Derosa, C. Di Lucca, T. Faillace, C. Figliuolo, V. Targiani, R. Davanzo

2020/3 — pag. 54-56

Branchial arch anomalies (sinuses, fistulae, cysts and condral remnants) represent one of the commonest paediatric neck malformations. The paper describes a case study of a 2-year-old girl who presented with a persistent left-sided ear drainage, unre...

Una torsione ovarica intermittente

A.G. Grasso

2020/2 — pag. 126

La torsione ovarica e tubarica in età pediatrica

A. Ravaglia, C. Vassia

2020/2 — pag. 111-116

Adnexal torsion is a surgical emergency defined as the total or partial rotation of ovary, fallopian tube or both around the vascular axis resulting in impaired blood flow with consequent ischemic injury. Misdiagnosis or delay in treatment may lead...

Infiammazione cronica e arterite di Takayasu

M. Cernich, L. Baggio, M. Guarnieri

2020/1 — pag. 23-23

La regola delle 3P: Pancreas + Pancialgia = Porpora

F. Cossovel, M. Londero, A. Taddio, G. Cozzi, A. Saccari, E. Guida, E. Barbi

2020/1 — pag. 4-6

A six-year-old boy was diagnosed as having Henoch-Schönlein purpura for a typical rash appearing after an episode of recurrent intussusception with signs of pancreatic involvement. While a delayed appearance of the cutaneous rash after intestinal int...

Doppio distretto renale con sbocco ureterale vaginale

I. Buffoni, G. Vagelli

2019/9 — pag. 596-598

Urinary dribbling in children can be due to urinary tract infection, mellitus and insipidus diabetes and vaginal voiding. In duplex renal system ureteral ectopia should be ruled out. Imaging of urinary tract in children is largely based on ultrasound...

Un’inaspettata convulsione… epatica

B. Cristiani, M. Di Pietro, G. Tezza, H. Egger

2019/9 — pag. 233-233

La sindrome di Beckwith-Wiedemann

A. De Paoli, A. Di Francesco, A. Selicorni

2019/8 — pag. 509-517

Beckwith-Wiedemann syndrome is a multisystemic disease mostly caused by genomic imprinting pattern anomalies of the 11p15.5 region. BWS is characterised by a very wide clinical spectrum starting from the more classical form (overgrowth, macroglossia,...

Ematemesi rivelatrice

R. Pillon

2019/8 — pag. 207-207

Uno stridore a recente insorgenza

G. Lanzoni, F. Maschio, P. Berlese, C. Zanatta, P. Midrio

2019/8 — pag. 206-206

Uso degli alfa-antagonisti nella calcolosi renale in età pediatrica: quali evidenze?

L. Facchini, S. Pusceddu, L. Casadio, F. Marchetti

2019/7 — pag. 445-448

Alpha-antagonists as an expulsive therapy for ureteral stones are widely recognized in adults. On the basis of the evidence in the literature, in children/adolescents with a kidney stone < 12 mm after the failure of the conventional therapy (hydrat...

Agenesia rotulea, ipoplasia ungueale e nail-patella syndrome

F. Baldo

2019/7 — pag. 150-150

Lingua nigra villosa

I. Antonello

2019/6 — pag. 128-128

Polipo e invaginazione intestinale

G. Lanzoni, P. Moras, D. Gobbi, P. Midrio

2019/5 — pag. 113-113

Le mille facce del Meckel: dal dolore alla perforazione

D. Codrich

2019/5 — pag. 111-112

Cisti ovarica feto-neonatale complicata con torsione e autoamputazione

V. Genchi, N. Laforgia, F. Caroppo, M.P. Lanzilotto, G. Paradies

2019/5 — pag. 104-107

The paper reports a case of ovarian cyst discovered in pregnancy, complicated with torsion and subsequent auto-amputation and migration in contact with the sigma. It underlines the fundamental role of imaging, especially during pregnancy, and of ultr...

Chirurgia indimenticabile: massa addominale con il volvolo

E. Guida

2019/4 — pag. 255-257

Troppo stanca troppo presto: la leucemia mielomonocitica giovanile

S. Contorno

2019/4 — pag. 95-95

Vomito sospetto biliare: pensa al chirurgo

M. Frigeri

2019/3 — pag. 191-192

Manifestazioni dell’infezione da virus di Epstein-Barr nel paziente con immunodeficit

F. Zunica, F. Saettini, A. Biondi, R. Badolato

2019/3 — pag. 163-169

Recurrent respiratory infections are frequent in healthy children. The association with peculiar signs and symptoms such as splenomegaly, lymphopenia, and hypogammaglobulinemia should induce suspicion of primary immunodeficiency (PID). The describe...

Le molte facce della istiocitosi a cellule di Langerhans

L. Picciano, R. Mancusi, M.C. Fedele, F. Palladino

2019/3 — pag. 52-52

Un ombelico… troppo spesso bagnato

D. Ferrara, L. Alessi, F. Mulè, G. Corsello

2019/1 — pag. 41-43

L’idrosadenite suppurativa nella popolazione pediatrica

B. Bossini, M. Mazzolai, A. Tommasini, S. Crovella, I. Berti, E. Barbi

2019/1 — pag. 28-32

Hidradenitis suppurativa (HS) is a chronic and recurrent skin disease affecting apocrine gland-bearing regions. Typical lesions are nodules and abscesses that result in sinus tracts, fistulas and eventually scarring. Prepubertal onset of HS is quit...

Storia di una tumefazione del collo ricorrente, troppo ricorrente

E. Fabbri, L. Bardeggia, A. Pedini, F. Libertucci, L. Viola, C. Cola, F. Tucci, R. Devito, G. Vergine

2018/10 — pag. 664-666

The paper describes the case of a 3-year-old girl who was repeatedly hospitalised for a swelling on her neck, which showed a scarce response to the antibiotic therapy, was significantly recurrent and was associated with fever and a remarkable increas...

Pile

S. Vignola, G. Ottonello, P. Gianiorio, A. Lavagetto

2018/10 — pag. 662-663

Storia di una tumefazione del collo ricorrente, troppo ricorrente

E. Fabbri, L. Bardeggia, A. Pedini, F. Libertucci, L. Viola, C. Cola, F. Tucci, R. Devito, G. Vergine

2018/10

The paper describes the case of a 3-year-old girl who was repeatedly hospitalised for a swelling on her neck, which showed a scarce response to the antibiotic therapy, was significantly recurrent and was associated with fever and a remarkable increas...

Papule piezogeniche Granulomi anulari multipli

2018/9 — pag. 598

Hai un monorene congenito? Il buon giorno si vede dal mattino!

M. Diplomatico, S. Guarino, N. Della Vecchia, T. Esposito, R. Marotta, P. Marzuillo

2018/9

Un’area di cute apparentemente glabra

2018/7 — pag. 467-468

Una cefalea che non ti aspetti: Moyamoya

P. Zagni, F. Leo, V. Loizzo, M.C. Bariola, G. Cingolani, L. Iughetti

2018/7

Dolore addominale in fossa iliaca destra: sembrava un'appendicite ma era una torsione dell’omento

C. Marchetti, C. Scalamogna, A. Mussari, R. Mattei

2018/6

The primary omental torsion is a rare cause of acute abdomen in the paediatric population. This condition occurs when the omental apron pedicle twists around its longer axis, leading to oedema, ischaemia and necrosis. The article describes a rare cas...

Gastroenterologia pediatrica: quattro casi per quattro messaggi

M. Bramuzzo

2018/5 — pag. 315-318

The present paper shortly describes four cases and gives some useful remarks to paediatricians about four gastroenterological conditions: sclerosing cholangitis, intestinal polyps, isolate rectal ulcer and early onset inflammatory bowel disease....

Latenza diagnostica in un adolescente con morbo di Crohn: esordio insidioso o diagnosi intempestiva?

A. Casertano, M. Martinelli, A. Staiano

2018/5

Un lattante che fa i calcoli

V. Dolcemascolo, E. Miorin, E. Vidal, P. Cogo

2018/1 — pag. 55-56

The paper presents the case of a four-month-old infant with a history of crying spells, vomit and renal stones on ultrasounds. Urinary excretion of dibasic amino acids and genetic study confirm a digenic cystinuria. The presented case shows that clin...

La gestione delle ustioni passo per passo

C. Santelia, C. Zanin

2018/1 — pag. 47-49

Lunga vita al rene! L'outcome dei reni unici congeniti

G. Macchini, A. Allegorico

2018/1

La sindrome di Pallister-Killian

L. Bettini, S. Tajè, A. Selicorni

2017/10 — pag. 657-658

Un ragazzo con episodi sub-occlusivi intestinali recidivanti

M. Mainetti, G. Turlà, C. Radice, I. Montroni, G. Ugolini, F. Marchetti

2017/10 — pag. 649-651

Masse ovariche perinatali, in età pediatrica e in adolescenza: miti e realtà

M.C. Lucchetti, F. Morini

2017/10 — pag. 641-648

Ovarian masses are a relatively frequent finding either in perinatal or in paediatric and adolescent ages and are not always easy to interpret and manage. The same rules and protocols used in adult patients are generally adopted in the clinical app...

Pielectasie neonatiDosaggio della melatonina

2017/8 — pag. 533

Melena e... biscotti

G. Ferrara

2017/8 — pag. 530

Un neonato con ernia diaframmatica congenita “nato apparentemente sano”

A. Casertano, F. Di Dato, P. Di Costanzo

2017/8

L’anemia che fa male

A. Bonadies, G. Rispoli

2017/7 — pag. 465-466

Ipereosinofilia severa: un caso da non dimenticare

E. Santi

2017/6

IpermetropiaIrsutismo e alopecia androgeneticaLattanti al bivio

2017/5 — pag. 329

Storia di nei che parlavano di intestino

I. Festa, R. Caiazzo, S. Napodano, C. Coppola, L. Sessa, E. De Nitto, P. Marzuillo, C. Strisciuglio, L. Perrone

2017/5

Calprotectina elevata e polipi intestinali: quale relazione?

M. Mainetti, A. Zucchini, G. Turlà, A. Buzzi, F. Marchetti

2017/4 — pag. 256-258

n clinical paediatric practice faecal calprotectin, a protein derived from white blood cells, is a reliable, non-invasive and easy-to-perform marker, with a high positive predictive power to identify intestinal inflammation. It is very useful for the...

Sarcoidosi pediatrica: esiste davvero?

M. Giovannini, M. Luzzati, G. Ferrara, T. Giani, G. Simonini, R. Cimaz

2017/2 — pag. 119-122

Disordine somatico. Ovvero il bambino che non funziona Alla conquista... della West Shigella alla riscossa (almeno in Africa)? Fistole ano-rettali nel morbo di Crohn: un’arma in più? Toh, chi si rivede: l’otite Bambini che mangiano senza appetito

2017/1 — pag. 11-12

Brucellosi: un raro caso di recidiva

M.C. Castiglione

2017/1

È tutta colpa di Currarino

V. Silecchia, M. Magnani, M. Cananzi, B. Giorgi, M. Marchiori, C. Vallongo

2016/9 — pag. 596-598

Quando la genetica ti cambia le carte in tavola

M. Pasetti, F. Crosti, S. Maitz, C. Fossati, V. D’Apolito, A. Selicorni

2016/7

La pelle e l’adolescenza

M. Cutrone, I. Berti

2016/4 — pag. 237-243

Una tonsilla che ricresce

C. Retetangos

2016/4

Radiografia del torace: come si osserva

A. Delise, V. Guastalla

2016/3 — pag. 183-184

Questo clistere non s’ha da fare

A. Russo

2016/2

Le solite coliche

G. Boschi

2016/1 — pag. 53-54

Un forellino nel padiglione auricolare

E. Mazzoni, M.T. Bartolini, G. Natali, A. Lambertini

2015/10 — pag. 657-658

Quelle strane chiazze...

D. Ferrara, G. Moceri, D. Vecchio, M. Milioto, G. Corsello

2015/8 — pag. 523-525

Calcolosi biliare: non solo per adulti...

G. Rossi, F. Cirillo, M. Sciveres, S. Riva, C. Ricotta, M. Spada, G. Maggiore

2015/8 — pag. 495-503

In recent years cholelithiasis has been on the rise among infants and children, partly because of improved diagnostic modalities, but also because of an increased awareness of emerging comorbidities, such as childhood obesity, and other associated ...

Casi indimenticabili (e trucchi del mestiere) Leucemia o artrite? Genetica: chi più spende meno spende? Vitamina D e polmoniti ricorrenti Coartazione aortica: brutta bestia anche con lo screening Vaccinazioni: chi la dura la vince? “San Cortisone” e artrite settica

2015/8 — pag. 485-486

Una febbre alta e persistente con epatosplenomegalia e citopenia

L. de Seta, M.S. Sabatino, F. de Seta, P. Siani

2015/7 — pag. 431-441

The case described is that of an 11-year-old child presenting with high fever, pharyngotonsillar exudate, submandibular strangles and hepatosplenomegaly. The elevated number of VCA IgM antibodies led to a diagnosis of infectious mononucleosis. The ...

Follow up a lungo termine dei pazienti con ernia diaframmatica congenita

M.V. Abate

2015/7

Quando la sferocitosi incontra il chirurgo

C. Bibalo

2015/6 — pag. 391-392

Summary Hereditary spherocytosis is a common inherited disorder that is characterized by anaemia, jaundice and splenomegaly. It is reported worldwide and is the most common inherited anaemia in individuals of northern European ancestry. Clinical ...

Un mal di pancia da... INFARTO!

V. Dolcemascolo, M. Arigliani, E. Passone

2015/4

Anomala in origine

F. Marolla

2015/4

La secrezione ematica dal capezzolo sotto l’anno di vita

L. Scurati-Manzoni, E. Finale, G. Melis, A. Guala

2015/3 — pag. 177-180

Bloody nipple discharge very rarely occurs in infants and often is associated with benign mammary duct ectasia. Just because it is a rare symptom and frequently associated with adults’ mammary cancer, it is inadequately managed: inappropriate diagn...

Isolati, multipli, ereditari: le tante facce dei polipi intestinali

C. Pierobon, M. Flammini, V. Moressa, S. Martelossi, A. Ventura

2015/1 — pag. 16-24

This article provides a critical review of the clinical presentation, pathology, genetics and management of the polyposis in childhood starting from the isolated juvenile polyp to the hereditary polyposis syndromes. These include the juvenile polyp...

Un ragazzo con la pancia piena

A. Maietta, M. Minute

2015/1

Wandering spleen in età pediatrica

L. Radillo, M. Maschio, A. Taddio, S. Furlan, E. Barbi

2014/10 — pag. 659-662

Il timo ectopico nella diagnosi differenziale delle masse del collo

M.C. Pellegrin, G. Patti, E. Faleschini, G. Tornese, P. Guastalla, A. Ventura

2014/9 — pag. 579-584

Ectopic thymus is a rare benign cause of paediatric neck masses. Because of embryologic migrational defects, ectopic thymic remnants can be found along the descent pathway from the mandible angle to the superior mediastinum. Clinically, between 2 ...

Nefrocalcinosi da povertà

E. Zanelli, P. Tommasi, M. Della Rocca, G. Zuin, M. Frediani, M. Fontana

2014/9

Tumefazioni ombelicali o quasi

C. Pierobon, A. Bon, R. Lualdi, L. Fasoli

2014/4 — pag. 255-256

Roberto Burgio (e Medico e Bambino) Il cervello autistico: troppi neuroni e mal disposti Evviva l’acidità gastrica Sirolimus nell’iperinsulinismo primitivo. Ovvero: evviva la ricerca L’importanza di trattare “subito” l’infezione urinaria Quando basta un gene… per fare una MICI Ospedali: meno infermiere, più morti Vaccinazioni: è possibile convincere? Ceftriaxone e calcoli renali

2014/4 — pag. 215-216

Al di là dell’occhio!

G. Ferrara, E. Zanelli

2014/3

Linfoadenite monolaterale con milza "impallinata": quale diagnosi?

A. Zucchini, P. Ricciardelli, F. Marchetti

2014/1 — pag. 54-56

Colelitiasi in età pediatrica: uno studio retrospettivo su 41 pazienti

G. Rossi, S. Nastasio, G. Marsalli, S. Ghione, C. Tuoni, G. Maggiore

2013/10

Quando il farmaco fa la differenza

G. Masia, C. Cubaiu

2013/8

Legami di sangue

C. Pierobon, A. Pirrone, M. Chinello

2013/8

Miocardite: la grande simulatrice

E. Benelli, M. Starc, E. Berton, M. Anzini, A. Benettoni, A. Ventura, G. Sinagra

2013/7 — pag. 429-434

Myocarditis is a rare, but life threatening disease in childhood. It is most often due to common viral infections; less commonly, it may result from bacterial infections, immune mediated diseases or chemotherapy. Myocarditis may present with unspec...

Tante visite, una diagnosi “by proxy”: ALPS, la sindrome linfoproliferativa autoimmune

L. Sirianni, M. Mancuso

2013/1

Autoimmune lymphoproliferative syndrome or ALPS is a genetic disease associated with anomalous apoptosis in lymphocytes, lymphoproliferation and autoimmune manifestations. Generally, it is possible to observe severe lymphadenopathy, hepatosplenomegal...

Due volti per uno stesso quadro …

G. Turlà, G. Guerrini, N. Zanforlini, MR. Contiero

2012/9

Fegato grosso e grasso: poche diagnosi a cui pensare

M. Mainetti, M. Grassi, A. Zucchini, L. Mambelli, F. Dal Monte, D. Cassandrini, G. Maggiore, F. Marchetti

2012/8 — pag. 533-534

The case of an 8-year-old girl with an isolated hypertransaminasemia asymptomatic without cholestasis and with moderate hypercholesterolemia and hepatomegaly with steatosis and glycogen storage in biopsy is described. Once excluded the commonest ...

Leishmania: un parassita, molte infezioni

S. Virano, D. Le Serre, S. Garazzino, E. Silvestro, P.A. Tovo

2012/8

A 10-year-old child presented with persistent fever, relevant hepatosplenomegaly and pancytopenia. Abdominal US imaging, serology for most relevant pathogens and Leishmania, PCR for Parvovirus B19 and bone marrow sample were performed in order to...

"Il cuore non si conta"Tachicardia parossistica sopraventricolare in un neonato

M. Mainetti, G. Piccinini, C. Renzelli, F. Marchetti, G. Bronzetti

2012/6

The case of a 12-day-old boy with supraventricular tachycardia (SVT) is reported. SVT in newborns is a relatively rare disease with only a few cases per year at each perinatal centre. The acute treatment of a single episode of SVT has generally a...

La pediatria per sigle: un neonato con il RICH

L. Mambelli, L. Pini, M. Baruzzi, F. Marchetti, F. Arcangeli

2012/5

Caverne

E. Ugolini, P. Fioretti

2012/4 — pag. 259-260

Una bambina con sanguinamento intestinale cronico occulto: utilità e limiti della videocapsula endoscopica

A. Montemaggi, J. Barp, C. Bonaccini, C. Fancelli, M. Milla, P. Lionetti

2012/2 — pag. 125-126

Meckel’s diverticulum is the most common congenital malformation of the gastrointestinal tract due to persistence of the congenital omphalomesenteric duct. Bleeding from Meckel’s diverticulum due to ectopic gastric mucosa is the most common clini...

Il diverticolo di Meckel nell’era della videocapsula: una diagnosi un po’ meno difficile

G. Patti, M. Bramuzzo, G. Di Leo, S. Martelossi, A. Ventura

2012/2 — pag. 107-110

The possibility of using video capsule endoscopy for diagnosing is known. Nevertheless only case reports or small case series have been published to date. Data of patients referred to our Pediatric department who were diagnosed with Meckel divertic...

L’eccesso di diagnosi e trattamento per il presunto reflusso gastroesofageo

F. Marchetti

2012/2 — pag. 99-101

Ritenzione della videocapsula nei pazienti pediatrici con MICI

N. Giurici

2012/2

Un addome sottosopra

S. Venezia, S. Osmi

2012/2

Un capello...di troppo!

L. Eliana Gazzola

2011/8

Sindrome di Klippel-Trenaunay

2011/4 — pag. 250-251

Attenzione alla schiena

M. Innocente

2011/3

Una famiglia a strisce...

I. Berti

2011/1

Un’incoercibile epigastralgia notturna

E. Modestini, D. Simongini

2010/8 — pag. 525-526

Vomito da malrotazione intestinale a esordio tardivo

M. Vestri, V. Gentilino, A. Montemaggi, A. Becocci, D. Bartolomeo, A. Messineo, P. Lionetti

2010/6 — pag. 397-398

Intestinal malrotation (IM) is a rare congenital alteration of the embryonal development of the bowel that typically presents in the first year of life. The Authors introduce the case of a 5 years old child affected by a chromosomal disorder (par...

Vomito da malrotazione intestinale a esordio tardivo

M. Vestri, V. Gentilino, A. Montemaggi, A. Becocci, D. Bartolomeo, A. Messineo, P. Lionetti

2010/6

Milza contorsionista

G. Cozzi, M. Maschio, E. Barbi

2010/6

Dolori addominali ricorrenti da invaginazione intermittente.Un caso di sindrome di Peutz-Jeghers in una bambina di 13 anni

M. Mainetti, S. Bevilacqua, M. Vestri, A Montemaggi, C. Fancelli, M. Prato, P. Lionetti

2010/2 — pag. 125-126

Peutz-Jeghers syndrome (PJS) is a rare, though well-described, hereditary disorder characterized by mucocutaneous pigmentation and hamartomatous polyps that typically present in the second decade of life. The Authors describe a case of a 13 year-...

Mangia calcio, se hai i calcoli!

2010/2 — pag. 123-124

Dolori addominali ricorrenti da invaginazione intermittenteUn caso di sindrome di Peutz-Jeghers in una bambina di 13 anni

M. Mainetti, S. Bevilacqua, M. Vestri, A. Montemaggi, C. Fancelli, M. Prato, P. Lionetti

2010/2

Una gambina più grossa

M.G. Scala, M. Mayer

2010/1 — pag. 55-56

The Authors describe a case of isolated hemihyperplasia (HHI) diagnosed on a three-month-old female child. During a visit at our pediatric surgery disproportion of the limbs was noticed, so the child was sent to genetic counselling. HHI diagnosis...

Una gambina più grossa

M.G. Scala, M. Mayer

2010/1

La fistola coronarica in età pediatrica

S. Caputo, F. Quarantiello, G. Vetrano, B. Villari

2009/8

Alopecia bitemporale e strie di iperpigmentazione in lattante con ritardo psicomotorio

G. Ciana, M.C. Fertz, C. Sanesi, S. Demarini, V. Petix, V. Pecile

2009/3 — pag. 189-190

The careful classification of a psychomotor delay in an infant is often a difficult task for paediatricians. Many hospital admissions for clinical, instrumental and laboratory investigations, are often needed, even though an exact diagnosis is no...

Alopecia bitemporale e strie di iperpigmentazione in lattante con ritardo psicomotorio

G. Ciana, M.C. Fertz, C. Sanesi, S. Demarini, V. Petix, V. Pecile

2009/3

L'ipertensione arteriosa in età pediatrica: dall'inquadramento diagnostico alla terapia

A. de Cunto, M. Maschio, M. Pennesi, A. Benettoni

2008/4 — pag. 226-234

The epidemic of childhood obesity, the risk of developing left ventricular hypertrophy, and evidence of the early development of atherosclerosis in children would make identification and treatment of hypertension an important focus of physicians ca...

Un ragazzo sotto pressione...

I. Di Rabach, J. Bua, G. Tornese, A. Saccari, F. Minen, I. L'Erario

2008/4

La splenomegalia

M. Rabusin, F. Patarino

2007/8 — pag. 493-499

The spleen in infants and children is involved in a wide variety of pathological conditions. Splenic disorders may be isolated like splenic cysts or, more frequently, due to multiorgan or systemic disease including hepatic diseases, malignancy, hemo...

Un caso di eritrofagocitosi secondaria a leishmaniosi nell’entroterra friulano

F. Minen, C. Oretti, F. Marchetti, G. Zanazzo, M. Maschio, D. Lizzi, A Ventura

2007/5 — pag. 325-327

The present report describes the case of a 2-year-old girl that lives in Northern Italy suffering from a one month lasting fever, pallor and hepatosplenomegaly. Serum testing showed pancytopenia, high levels of immunoglobulins, hypertriglyceridemia a...

Una strana epatite autoimmune

G. Maggiore

2007/5 — pag. 320

Una milza enorme...

Mario Furbetta, Stefanie Rempp

2007/4 — pag. 255-256

Russare: un disturbo banale?

C. Gussoni

2007/4

Dolore addominale, distensione gastricae vomito biliare

C. Oretti, F. Marchetti, D. Codrich, G. Pelizzo, P. Guastalla, D. Lizzi, A. Ventura

2007/1 — pag. 45-47

Dolore addominale ricorrente e vomito, con riscontro di formazione anecogena addominale

D. Codrich, A. Taddio, P. Salierno, C. Furlan, F. Marchetti

2006/10 — pag. 663-664

Steroidi inalatori e storia naturale dell'asma bronchiale

D. Radzik

2006/10 — pag. 656-660

Background Airway chronic inflammation and remodelling play an important role in the pathophysiology of asthma, leading to structural irreversible changes of the airways which occur already in the early school years. Objective To determine whether a...

Ernia diaframmatica congenita: un problema non solo neonatale

M. Don, B. Sacher

2006/10 — pag. 631-641

Congenital diaphragmatic hernia (CDH) is a relatively common disease which depends on the passage of some abdominal organs into the chest cavity. Its incidence is of 1 in 3000 live births. CDH aetiology has not been yet fully established, but hypopla...

Ipertrofia clitoridea in bambina affetta da neurofibromatosi di tipo 1

E. Ballerini, R. Luksch

2006/9 — pag. 601-602

We report the case of NF1 in a 21 month old female, who presented with hypertrophy of the clitoris. The work-up evaluations revealed the presence of multiple pelvic and abdominal neurofibromas and concomitant histologically assessed presacral ganglio...

Ipertrofia clitoridea in bambina affetta da neurofibromatosi di tipo 1

E. Ballerini, R. Luksch

2006/9

Sangue e muco nelle feci

J. Bua, S. Norbedo, S. Martelossi

2006/2

Per fortuna ci sono gli esami!

D. Lizzi

2005/10 — pag. 668

Le valvole uretrali anteriori: descrizione di un caso clinico

A. Borrelli, A. Correra, D. Ummarino

2005/10

Asma lieve persistente: cortisone solo quando stanno maleAsma: il remodelling è precoce e non si modifica più, qualsiasi terapia venga fattaAutoimmunità, sistema nervoso centrale e streptococcoIncidenza di anticorpi anti-SNC e disturbi ossessivo-compulsiviROMA - Un ragazzo di 17 anni è morto, UDINE «Se ti spogli ti votiamo»â€¦e altro ancoraChernobyl, niente tracce sui bimbi in ItaliaAmbiziosi si nasceIndia, bambina nata con il cuore esterno in una manoSalute materno infantile: obbligatorio garantirla a tuttiI cibi dolci aumentano il rischio di tumore al senoIn America viene inserito nel calendario vaccinale la vaccinazione per epatite A

I. Bruno

2005/9

Quando iniziare e quando sospendere i farmaci antiasmatici

L. Travan, I. Berti, G. Longo

2005/3 — pag. 157-163

The understanding of the chronic bronchial inflammation characterizing asthma led us to a more convinced and accurate use of inhaled corticosteroids such as long lasting therapy. Although times and ways for this treatment have been defined by sever...

Un bambino con ano imperforato

L. Calligaris, S.Norbedo, R. Davanzo

2004/11

Malattie mitocondriali e malattia infiammatoria cronica intestinale a esordio nei primi mesi di vita“Se solo avesse smesso di piangere, non l’avrei picchiato”Diabete infantile e arteriosclerosi subclinicaCeftriaxone e calcoli (renali)Fluticasone inalatorio: est modus in rebus. O se volete: il farmaco migliore può essere il peggioreTumore di Wilms: sempre meglio, sempre con menoComunicazione col paziente, in Inghilterra “Per legge”

2004/10 — pag. 611-612

Trattamento della sindrome di Wolff-Parkinson-White

G. Bartolozzi

2004/9

Una dattilite bilaterale simmetrica

M. Lazzerini

2004/2

Una dattilite bilaterale simmetrica

M. Lazzerini

2004/2

Una dattilite bilaterale simmetrica

M. Lazzerini

2004/2

Domande e risposte

2004/1 — pag. 57

Ha preso tutto da papà (alopecia occipitale del neonato)

M. Cutrone

2003/10 — pag. 679-680

Storia di una famiglia con sindrome di Peutz Jeghers: importanza dello screening strumentale anche nei soggetti asintomatici

S. Centuori, S. Martellossi, L. Ammar

2003/9

Storia di una famiglia con sindrome di Peutz-Jeghers: importanza dello screening strumentale anche nei soggetti asintomatici

2003/9 — pag. 606

Report on two brothers with PJS and a positive family history. The first one symptomatic from when was 16 months; the second one asymtomatic underwent to EGDS when fifteen and after endoscopic removal of 6 polyps (the biggest >3 cm) develop emorra...

Ittero tardivo e atresia delle vie biliariTra il dire e il fare: ITra il dire e il fare: IIRisposte fisiologiche a fisiologici bisogni

2003/3 — pag. 149-151

Lesioni misteriose sulla pelle del neonato

G. D’Asero, E. Scaffidi

2002/10 — pag. 680

Malaria: diagnosi tempestiva

2002/9 — pag. 606-606

Report of a malaria case (temperature, convulsions, anaemia, splenomegaly) back from a trip to Africa....

Diarrea acquosa in una bambina di 22 mesi

G. Bartolozzi

2002/4

Ittero colestatico in un bambino di un meseUn caso clinico personale di 10 anni fa

G. Bartolozzi

2002/3

Il testicolo ritenuto

F. Raimondi, M. Bussi, L. Capasso, et al.

2002/2 — pag. 116-120

To improve the knowledge on natural history and medical practice relating to undescended testis (UT), the records of 7199 male births were reviewed. Cases with UT were assessed and classified and all subjects with abnormal findings at birth were re...

Insufficienza dell'acetazolamide e della furosemide nel trattamento della dilatazione postemorragica ventricolare del prematuro

G. Bartolozzi

2001/10

Incontinentia Pigmenti

S. Marinoni, T. Bardaro

2001/10

Malattia emolitica neonatale (MEN) da basso peso per l’età gestazionale (SGA) con anemia diseritropoietica congenita (CDA) tipo I

L. Lupi, C. Visone

2001/5 — pag. 331-331

Report of a case of Congenital Dyserythropoietic Anaemia (CDA) of type I, clinically expressed since the first day of life, with colostatic jaundice, macrocitic anaemia, splenomegaly. Retrospective analysis of 17 cases of CDA....

Su un caso di febbre periodica ... un anno dopo (Ovvero: PFAPA+Adenovirus+MICI)

F. Sellitto, R. Rabuano, A. Basilicata

2001/4

Sindrome di beckwith-wiedemann.macroglossia e crescita cranio-facciale:considerazioni e proposte

E. Viva, E. Viva, M. Ruggiero, L. Ruggiero

2001/3 — pag. 191-192

Description of a Beckwith-Wiedemann syndrome case (annular hernia with rectal diastase; neonatal visceromegaly, then regressed; macrosomia, then regressed; macroglossia; other minor anomalies). This case is peculiar because it is relatively not se...

Iponatremia e coma dopo un intervento chirurgico senza fattori di rischio

E. Garbagnati

2001/2

Coma iponatremico post-chirurgico

E. Garbagnati

2001/2 — pag. 122-122

Case description of deep hyponatremic coma (115 mEq/l), with ischaemic focus in left parietal, which lasted over 24 hours and returned almost to normality (persistence of slowing down of speech) within 10 days. This episode followed a bilateral in...

Ernia diaframmatica congenita: un caso di diagnosi tardiva.

A. Giannotta, E. Chiella, D. Codrich, M. Monai, L. Paduano, G. Pelizzo, A. Messineo

2001/1

Agenesia polmonare e sindrome di goldenhar

P. Costantini

2000/8 — pag. 531-532

Description of a monolateral pulmonary agenesis case, which was identified at birth thanks to a pre-surgical radiological chest examination. A discrete dyspnea and a significant polyglobulia ensured a compensation of agenesis without desaturation....

Fibro-endoscopia dell’ostruzione del cavo rino-faringeo da iupertrofia adenoidea

F. Cassano, M. Gelardi

2000/4 — pag. 239-244

Transnasal fiberendoscopy of the nasopharinx is the easiest and most effective way to assess adenoidal hypertrophy in children. On this basis, the Authors proposed a 4-stage classification to guide the case management: the first two stages are char...

Macroematuria associata a ipercalciuria

C. Polito, A. La Manna, E. Varricchio, R. Maiello, A. Marte

2000/3 — pag. 191-192

Sindrome acrocallosa in neonato (il contributo diagnostico dell'ecografia)

M. Budetta, I. Andreozzi

2000/1

Diverticolo di meckel non complicato: una diagnosi difficile

M. Monai, A. Giannotta

2000/1 — pag. 57-58

La 34° visita di pronto soccorso pediatrico: un caso di hair thread tourniquet syndrome

M. Cutrone

1999/10 — pag. 662-663

La sindrome acrocallosa

M. Budetta

1999/10 — pag. 657-658

Calendario chirurgico

A. Messineo

1999/10 — pag. 627-628

The timing and treatment of a few common surgical conditions are discussed. Inguinal hernia should be surgically treated as soon as possible. Funicular cyst and hydrocele can wait until the end of the second year. Testes must be in their scrotal si...

Cisti aracnoidea associata a nevo di becker

C. De Meco, M. Crisetti, M. Germano, M.I. Jussi, P. Paolucci

1999/8 — pag. 471-472

Una "mici" da micio

G. Maggiore

1999/8 — pag. 516

TNF e fistole addominali della m. Di CrohnTh1/Th2 : atopia e asma, basso peso alla nascita, diabete TBAcidi grassi trans e atopiaLa diagnosi di pertosse è difficileInefficacia della cisapride: l'allegro rigurgitatoreVomito ciclico ed emicraniaGH nella sindrome di TurnerAlloicoccus otitis e OMEFumo materno e malattie dell'orecchio medioProcubito e SIDS: perché ?Invaginazione intestinale e vaccinazione contro i rotavirusLo pneumococco resistente ai fluorochinoloniVitamina A, malaria e broncopneumodisplasia

G. Bartolozzi

1999/7

Una calvizie troppo precoce

M. Cutrone

1999/6 — pag. 381-382

Un caso istruttivo di disostosi spondilometafisaria

D. Bello

1999/2

Trattamento steroideo locale dell'ipertrofia adenoidea e tonsillare: uno studio retrospettivo

A. Mendoza, F. Panizon

1999/1

Trattamento con steroidi topici dell’ipertrofia adeno-tonsillare

A. Mendoza, F. Panizon

1999/1 — pag. 13

Una splenomegalia febbrile con neutropenia

C. Malorgio

1998/9

Una splenomegalia febbrile con neutropenia

P. Tamaro, C. Malorgio

1998/9 — pag. 581

Il caso di maicol: uno strano "valsalva"

S. Castelli

1998/8 — pag. 543-544

Le malformazioni dell’uraco

M. Porrello

1997/9 — pag. 595-597