Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
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Leukocyte Disorders

131 articoli — 1997-2026 Include sottocategorie MeSH

EL Caso contributivo
Immunodeficienza combinata grave

Valencic I, Moratti M, Bettelli S, Ancora G

2026/3 — pag. 58-66 — DOI

Severe combined immunodeficiency (SCID) is characterised by profound quantitative and/or functional T-cell defects and predisposes infants to life-threatening infections, including sepsis that may progress to organ dysfunction and disseminated intrav...

RI Dermo mail
Porpora di Schönlein-Henoch bollosa Mononucleosi

2025/10 — pag. 668 — DOI

RI Se la conosci la riconosci
La sindrome di Barth

Dobbiani G, Crapanzano C, Tovaglieri N.

2025/10 — pag. 654-657 — DOI

RI Casi indimenticabili
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...

EL I Poster degli specializzandi
Accesso libero
Quanti danni questi eosinofili!

Cannas M, Malaventura C

2025/8 — pag. 218-219 — DOI

A 15-year-old boy presented with abdominal pain, weight loss, ascites and marked eosinophilia. Work-up excluded infectious, autoimmune and neoplastic causes, leading to the diagnosis of hypereosinophilic syndrome with transmural panenteric involvemen...

EL Casi indimenticabili
Polmoni di ferro

Pascolo P, Cotić I, Krivec U

2025/7 — pag. 188-189 — DOI

An extremely premature infant (24 weeks’ gestation, birth weight 380 g) with congenital heart disease and severe bronchopulmonary dysplasia is hospitalized for worsening respiratory function, hypoxia and rising eosinophilia in the absence of infectio...

EL Caso contributivo
La macroematuria che non ti aspetti

Bossalini G, Gaudenzi F, Sodero R, Grosso SN, Coppola C, Valentino MS, Caiazzo R, Giacomet V

2025/6 — pag. 148-151 — DOI

Macrohaematuria and microhematuria may be signs of various diseases. Infectious haematuria often presents with fever and/or dysuria. The paper describes the case of a 14-year-old boy from Mali who was in Italy for five months and presented with gross...

RI Binomi
Mal di schiena (e... null'altro) Dolore e "rumore"

2025/4 — pag. 225-228 — DOI

RI Pagine elettroniche
Colecistite acuta da EBV

Favaretto E.

2025/1 — pag. 52-55 — 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...

EL I Poster degli specializzandi
Accesso libero
La diagnosi di artrite idiopatica giovanile sistemica

Basilio P

2024/7 — pag. 140-140 — DOI

A 9-year-old boy presented with persistent fever, joint pain and productive cough not responding to antibiotic treatments. After negative diagnostic tests, a fleeting rash during a fever spike and neutrophilic leukocytosis led to the diagnosis of sys...

RI Aggiornamento
Difetti congeniti dell’immunità: non solo le vecchie immunodeficienze

Tommasini A, Valencic E, Naviglio S.

2024/4 — pag. 219-226 — DOI

Inborn errors of immunity are a rapidly-developing area of clinical study. Based on the description of a small set of disorders with a significant risk of infection that may be identified with a small number of lab tests, the definition has been expa...

RI Pagine elettroniche
Un inspirio insolito: la vocal cord dysfunction

Fracas D.

2024/3 — pag. 189-192 — DOI

The diagnosis of vocal cord dysfunction was eventually made in a 10-year-old boy with repeated self-limited episodes of inspiratory dyspnoea....

RI Pagine elettroniche
Quando il polmone ci suggerisce una immunodeficienza

Lo Scalzo L, Tumminello M, Corsello G

2024/3 — pag. 189-192 — DOI

A neonate affected by a severe respiratory infection was eventually diagnosed with severe combined immunodeficiency with hyper-IgE (Job syndrome)....

EL I Poster degli specializzandi
Accesso libero
Quando il polmone ci suggerisce una immunodeficienza

Lo Scalzo L, Tumminello M, Corsello G

2024/3 — pag. 58-58 — DOI

A neonate affected by a severe respiratory infection was eventually diagnosed with severe combined immunodeficiency with hyper-IgE (Job syndrome)....

RI Casi indimenticabili
Pensa alla bronchite eosinofila

Fusco F.

2023/10 — pag. 662-663 — DOI

The diagnosis of eosinophilic bronchitis was finally done in a 4-year-old girl with dry, long lasting cough...

RI Problemi speciali
Quando il boccone non va giù: la disfagia in Pediatria attraverso i casi

Capata G, Lega S, Bramuzzo M, Di Leo G.

2023/9 — pag. 575-579 — DOI

Dysphagia is a disorder that affects one or more phases of the swallowing process. In paediatric age, it is often difficult to discriminate the underlying cause of this disorder. In this sense, a first distinction between oropharyngeal and oesophagea...

RI Problemi speciali
Sindromi, genetica e immunologia: dall’inizio della fine alla fine dell’inizio

Guerra F, Saettini F, Biondi A.

2023/9 — pag. 569-574 — DOI

Syndromic immunodeficiencies are defined as a group of immunodeficiencies in which the immunological defect may be found only in a subgroup of patients. They fall within a more complex clinical picture and may not represent the primary clinical probl...

EL I Poster degli specializzandi
Accesso libero
Un caso complesso di citopenia trilineare ed epatite gigantocellulare

Comella M, Licciardello M, Miraglia V, Russo G

2023/8 — pag. 165-165 — DOI

The case of a five-year-old boy presenting with autoimmune anaemia, neutropenia and thrombocytopenia associated to giant cell hepatitis is described. The diagnosis of ALPS-like syndrome was eventually made....

RI Pagine elettroniche
Allarme rosso: il sanguinamento rettale

Fracas D, Di Leo G.

2023/7 — pag. 465-468 — DOI

A 6-week-old, exclusively breastfed and well-appearing infant presented with blood in her stools. A diagnosis of food protein-induced allergic proctocolitis was promptly made by the presence of the high number of eosinophils in her blood and the prom...

EL I Poster degli specializzandi
Accesso libero
Allarme rosso: il sanguinamento rettale

Fracas D, Di Leo G

2023/7 — pag. 135-135 — DOI

A 6-week-old, exclusively breastfed and well-appearing infant presented with blood in her stools. A diagnosis of food protein-induced allergic proctocolitis was promptly made by the presence of the high number of eosinophils in her blood and the prom...

RI Pagine elettroniche
Non c’è due senza DRESS

Paoletti B, Sollai S, Mirri S, Pelosi P, Brambilla A, Cupone R, Bini R, Cocchi C, Mori F, Ferrara G, Mirri G.

2023/6 — pag. 399-402 — DOI

EL Casi indimenticabili
Non c’è due senza DRESS

Paoletti B, Sollai S, Mirri S, Pelosi P, Brambilla A, Cupone R, Bini R, Cocchi C, Mori F, Ferrara G, Mirri G

2023/6 — pag. 102-103 — DOI

A diagnosis of DRESS (Drug Reaction with Eosinophilia and Systemic Symptoms) was finally made in a 15-year-old epileptic boy with itching maculopapular rash and high blood eosinophil count....

RI Pagine elettroniche
Febbre e gengivostomatite: non è sempre solo herpes simplex

Arnaboldi S.

2023/5 — pag. 331-334 — DOI

Gingivostomatitis is a clinical condition frequently diagnosed by the family paediatrician and it generally shows a viral aetiology. In particular, primary herpes simplex infection is the most frequent cause of gingivostomatitis in toddlers and it ty...

RI Pagine elettroniche
La polmonite da adenovirus

Zago A, Benvenuto S.

2023/4 — pag. 261-263 — DOI

The author describes the case of a 3-year-old boy presenting with cough and fever that had been persisting for seven days and not respondent to amoxicillin. Neutrophilic leukocytosis and diarrhoea were also present. The diagnosis of adenovirus infect...

RI Casi indimenticabili
Infezione da virus di Epstein-Barr: citopenia e colecisti ispessita

Benvenuto S.

2023/4 — pag. 260 — DOI

The author describes the case of a 13-year-old girl presenting with abdominal pain, thrombocytopoenia and neutropoenia. A thickened gallbladder was evident at abdominal sonography. The diagnosis of EBV infection, based on serological investigation, w...

EL I Poster degli specializzandi
Accesso libero
La polmonite da adenovirus

Zago A, Benvenuto S

2023/4 — pag. 75-75 — DOI

The author describes the case of a 3-year-old boy presenting with cough and fever that had been persisting for seven days and not respondent to amoxicillin. Neutrophilic leukocytosis and diarrhoea were also present. The diagnosis of adenovirus infect...

EL I Poster degli specializzandi
Accesso libero
Una MIS-C come possibile spia di errori congeniti dell’immunità

Drago E, Massaccesi E, Ridella F, Scalas M, Caorsi R, Fioredda F

2023/3 — pag. 52-52 — DOI

The Authors described the case of a 2-year-old child presenting with the typical clinical features of MIS-C finally diagnosed as Wiskott-Aldrich immunodeficiency....

EL Caso contributivo
Un caso insolito di trombocitopenia

Barachino A

2023/1 — pag. 4-5 — DOI

A two-and-a-half-year-old child presents with spontaneous ecchymosis. In addition to severe thrombocytopoenia, initial investigations show the presence of neutropoenia and signs of immune-mediated haemolysis (positivity of the direct antiglobulin tes...

RI Domande e risposte
Tosse secca persistente Asma e spirometria

2022/10 — pag. 659 — DOI

EL Caso contributivo
Fetal inflammatory response syndrome (FIRS): che cosa è, quando bisogna pensarci

Tagliani S, Casadio L, Bruno I, Graziani G, Radice C, Zago S, Piccinini G, Marchetti F

2022/10 — pag. 200-204 — DOI

The paper describes a case of severe hyperleukocytosis in a preterm with FIRS (Fetal Inflammatory Response Syndrome) associated with funisitis of umbilical cord and intrauterine inflammation. FIRS is a cause of leukocytosis in newborn, as well as leu...

RI Farmacoriflessioni
Il dupilumab nell’esofagite eosinofila: una nuova frontiera?

Mainetti M, Troisi A, Turlà G, Fontijn S, Rametta G, Buzzi A, Mussetto A, Marchetti F.

2022/9 — pag. 583-587 — DOI

Eosinophilic oesophagitis (EoE) is a chronic, immune-mediated or antigen-mediated oe-sophageal disease. Therapeutic first-line options currently available for EoE are elimina-tion diets, proton pump inhibitors (PPIs) and steroids. The ultimate goal o...

RI Casi indimenticabili
Travolti da un insolito destino nell’immenso mare degli eosinofili

Iannicelli A.

2022/6 — pag. 393-395 — DOI

The case of an adolescent with persistent cough and blood eosinophilia eventually diagnosed as idiopathic hypereosinophilic syndrome is presented. The diagnostic approach to hypereosinophilia is discussed....

RI Casi indimenticabili
Gastrite eosinofila: una causa di possibile anemia sideropenica

Brugnera G, Mario F, Martelossi S, Pavanello P, Pizzol A.

2022/6 — pag. 393-395 — DOI

A case of eosinophilic gastritis (EG) associated with severe iron deficiency anaemia is described. The authors recommend to consider EG in approaching the diagnosis of iron deficiency anaemia associated with intestinal bleeding....

EL I Poster degli specializzandi
Accesso libero
Sangue nel vomito… eosinofili nello stomaco

Paganin P

2022/6 — pag. 135-135 — DOI

The case of a 4-month-year-old infant presenting with blood vomiting eventually diagnosed as food protein-induced enterocolitis syndrome (FPIES) is described. The main clinical and diagnostic aspects of FPIES are also discussed....

RI Rubrica iconografica
Una tumefazione dell’osso in sede parietale

Roveran M, Benincasa C, Biserna L, Radice C, Romeo C, Fabbri E, Marchetti F.

2022/2 — pag. 115-116 — DOI

EL Caso contributivo
La sindrome "Cefalea e deficit neurologici transitori con linfocitosi liquorale": un’altra encefalopatia autoimmune?

Morelli ME, Carrozzi M

2021/8 — pag. 241-245 — DOI

Headache and neurologic deficits with cerebrospinal fluid lymphocytosis syndrome (HaNDL) is a rare nosographic entity, which mainly affects adults but can also occur in the paediatric age. In the literature, 31 cases in this age group are described. ...

RI Farmacoriflessioni
Tutto quello che il pediatra dovrebbe sapere sul mepolizumab

Prisco A, Carlone G, Maschio M, Badina L, Barbi E

2021/6 — pag. 374-378 — DOI

Mepolizumab, a monoclonal antibody blocking IL-5, is efficacious in the treatment of severe lung diseases sharing eosinophilic inflammation pattern. The paper describes two cases in which the drug was used with excellent results. The first involved a...

EL Caso contributivo
La sindrome di Chediak-Higashi a esordio tardivo

Ciancia S, Dalla Porta MF, Cingolani GM, Cellini M, Soresina A, Badolato R, Mariotti I, Cano Garcinuno MdC, Iughetti L

2021/4 — pag. 118-123 — DOI

Chediak-Higashi syndrome (CHS) is a rare autosomal recessive disorder caused by mutations in the CHS1/LYST gene, encoding for LYST protein, involved in lysosomal trafficking. It is characterized by recurrent bacterial infections, oculocutaneous albin...

EL Casi indimenticabili
Una FPIES in una neonata

Risso FM, Romano S

2021/1 — pag. 25-25 — DOI

Food protein-induced enterocolitis syndrome (FPIES) is a non-immunoglobulin E cell-mediated gastrointestinal food allergy that usually occurs in infancy. The paper presents and discusses a case of FPIES with neonatal onset....

RI Problemi speciali
La granulomatosi eosinofilica con poliangioite: dalla pelle al cuore

M. Pavan, A. Agrusti, A. Trombetta, S. Pastore, A. Tommasini, V. Moressa, F. Marchetti, A. Taddio, A. Ventura

2020/9 — pag. 569-574 — DOI

Background - Eosinophilic granulomatosis with polyangiitis, formerly known as Churg-Strauss syndrome, is an extremely rare systemic vasculitis in the paediatric population. The hallmarks of eosinophilic granulomatosis with polyangiitis are a long his...

RI Focus
Indagare cum “granuloma” salis: malattia granulomatosa cronica vs malattia di Crohn

C. Pantuso, M. Citrano, M. Giuffrè, G. Corsello

2020/5 — pag. 315-316

Chronic granulomatous disease (CGD) is a rare inherited disorder of phagocyte oxidative metabolism that, in addition to infectious complications, is characterized by abnormal inflammatory response leading to the formation of granulomas in multiple ti...

RI Focus
MALATTIA INFIAMMATORIA CRONICA INTESTINALE E DINTORNI

A. Ventura

2020/5 — pag. 314-314

RI News box
Accesso libero
Covid-19 e bambini: il punto dalla letteratura al 18 marzo

C. Guiducci, F. Marchetti

2020/3 — pag. 151-153

RI Domande e risposte
Naso sempre chiuso, disturbi somatoformi

2020/2 — pag. 131

RI Aggiornamento
Il bambino con i linfonodi ingrossati: una messa a punto attraverso i casi

E. Benelli, C. Zanatta, G. Muffato, V. Biscaro, M. Cacciatore, P. Grotto

2019/5 — pag. 289-296

Lymphadenitis is a common finding in Paediatrics. However, it could be a sign of many different diseases, varying from banal viral infections to severe neoplastic disease or immunodeficiency. Some clinical aspects can be useful to differentiate the...

RI Problemi speciali
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...

RI Problemi speciali
Leucociti: più alti che bassi

D.U. De Rose, R. Badolato

2018/7 — pag. 435-439

Leukocytosis is a common finding in children evaluation. In order to highlight the underlying cause, it is necessary to investigate which leukocyte subset is involved. Usually, leukocytosis is observed in children with infectious diseases. However,...

RI Casi indimenticabili
Un'anemia macrocitica in una ragazza di 13 anni

M.C. Pellegrin, A. Delise

2018/2 — pag. 115-117

EL Caso contributivo
Anticorpi anti-istone: è sempre lupus indotto da farmaci?

A. Azzali, T. Giani, G. Simonini, R. Cimaz

2018/2

The paper describes the case of a South-American 14-year-old girl who presented with arthralgia, weakness and alopecia. As she was under antiepileptic treatment since she was 5 years of age, on suspicion of drug-induced lupus erythematosus (DILE) ant...

RI Pagine elettroniche
Due zoppie per due diagnosi

F. Corrias

2017/7 — pag. 465-466

EL I Poster degli specializzandi
Accesso libero
Ipereosinofilia severa: un caso da non dimenticare

E. Santi

2017/6

RI Casi indimenticabili
Qualcosa di più di un "asma"

A. Iacono, P. Gallo, L. Pecorari

2017/3 — pag. 191-193

RI Aggiornamento
Le neutropenie del neonato

P. Farruggia

2017/2 — pag. 85-90

Neonatal neutropoenia is not infrequent. Its appearance can be linked to many serious or minor causes and it is necessary to provide an accurate overview in order to make the best decisions on its management. This paper takes into consideration som...

RI Percorsi clinici
La diagnosi differenziale delle malattie che si presentano con IgE alte

G. Patelli, S. Farimbella, M. Cortesi, R. Badolato

2017/1 — pag. 39-43

Elevated IgE levels (higher than 1500 UI) can be detected in multiple conditions observed in childhood, including atopic dermatitis, infectious diseases or primary immunodeficiencies. This article describes the case of a child who in the first year...

RI Domande e risposte
Maltrattamento sospetto Esofagite eosinofila e dieta

2016/9 — pag. 605

RI Pagine elettroniche
Può l'amoxicillina aumentare il rischio di rash nei casi di mononucleosi?

S. Pusceddu, V. Murgia, F. Marchetti

2016/6 — pag. 393-394

EL I Poster degli specializzandi
Accesso libero
Narici NARES

S. Lega

2016/3

RI Problemi speciali
Il bambino con infezione da micobatteri non tubercolari

M. Caironi, R. Badolato

2015/10 — pag. 634-638

Localized mycobacterial infections of cervical lymph nodes are frequently observed in normal children. These types of infections are sustained by environmental mycobacteria and can be treated by surgical therapy. On the contrary, disseminated mycob...

RI Focus
LA LINFOISTIOCITOSI EMOFAGOCITICA

2015/7 — pag. 431-441

RI Problemi speciali
La linfopenia nel bambino

C. Dallavilla, R. Badolato

2015/4 — pag. 239-246

Isolated lymphopoenia is a common finding in children evaluation. Usually, lymphopoenia is observed in children with infectious or autoimmune diseases, with nutritional disorders or under treatment with immunosuppressive drugs. However, persistence...

RI Domande e risposte
Angioedema ricorrenteDifetto interventricolare

2015/3 — pag. 198

EL Casi indimenticabili
La storia di Martina

V. Rossomando

2012/10

RI Ricerca
La sindrome mononucleosica: revisione di 107 casi

C. Geraci, M. Pocecco

2012/8 — pag. 521-523

Childhood infectious mononucleosis is a benign and self-limited disease. Complications are rare but not unremarkable: 3 out of 107 patients experienced haematological complications (1 autoimmune haemolytic anaemia and 2 autoimmune thrombocytopenia)...

RI Casi indimenticabili
Un caso di acrodermatite in un lattante

M. Barrani, F. Massei

2012/7 — pag. 465

RI Linee guida
Linee guida per la diagnosi e la terapia del reflusso gastroesofageo

Sintesi a cura di R. Cavallo

2012/2 — pag. 89-98

The documents contains 24 formal recommendations deriving from a joint assessment of all the literature that can be evaluated as well as from the experience of the members of the panel and unequivocally clarifies what is useful to do, namely what i...

RI Aggiornamento
L’ipereosinofilia

A. De Cunto, C. Geraci, E. Rubinato, G. Longo, A. Lorenzati, R. Mazzone, U. Ramenghi

2011/8 — pag. 499-504

Blood eosinophilia, especially if found fortuitously, often remains poorly understood. This article provides a diagnostic approach to hypereosinophilia, focusing on the context in which these data are found. The diagnostic evaluation of hypereosino...

RI Pagine elettroniche ; Caso Contributivo
Interessamento cardiaco nella sindrome di Churg-Strauss

A. Amaddeo, F. Marchetti, M. Londero, M. Maschio, A. Benettoni, A. Ventura

2011/4 — pag. 259-261

We report the case of a 15-year-old boy with asthenia, hypereosinophilia, a macular-papular rash in his hands and weight loss in the previous two months. Spirometry showed severe bronchial obstruction and transthoracic echocardiography revealed a...

RI Pillole: per capire
Dermatite e IgE alte

R. Badolato

2011/2 — pag. 107-109

A case of Job syndrome is presented. Job syndrome is linked to a dominant autosomal disorder of the gene that codifies an intracellular protein whose function is the transduction of receptorial signals from the membrane to the nucleus. This central...

EL Casi indimenticabili
Primo pomeriggio in PS

C. Zanchi, G. Cont, L. Rubert

2010/2

RI Pillole: per capire
Neutropenia da mielocatessi

R. Badolato

2009/1 — pag. 35-38

The works describes a case of WHIM (Warts, Hypogammaglobulinemia, Immunodeficit, Myelokathexis) characterized by neutropenia, hypogammaglobulinemia, reduced number of lymphocytes B (C19) in blood stream, and bone marrow rich in element of the myelo...

EL Appunti di Terapia
Accesso libero
Reazioni cutanee ai farmaci (parte terza)

G. Bartolozzi

2008/2

RI Problemi non correnti
L'esofagite eosinofila

J. Bua, F. Marchetti, I. Giuseppin, M. Marani, V. Villanacci, E. Barbi, S. Martelossi, A. Ventura

2007/8 — pag. 500-508

Eosinophilic esophagitis (EE) is the leading cause of dysphagia in children. Long underestimated in the past, it is nowadays reported with increasing frequency both in paediatric and adult gastroenterology. However, its natural history, its pathoge...

RI Pagine elettroniche ; Caso Contributivo
Un caso di zoppia

C. Galletto, N. Bertorello, E. Barisone, R. Mazzone, A. Andreacchio

2007/1 — pag. 51-53

In childhood and adolescence articular pains are frequent and in most of the cases they disappear rapidly and spontaneously. In a few patients the cause of the symptoms is an organic and/or a systemic pathology that require accurate examination a...

RI Percorsi clinici
Una bambina con febbre e schiena rigida

F. Marchetti, S. Bassanese, I. Bruno, et al.

2005/10 — pag. 669-671

EL Caso Clinico Interattivo
Accesso libero
Una disfagia per i cibi solidi in un ragazzo di 12 anni

L. Travan, P. Salierno, S. Martelossi

2005/7

EL Caso Clinico Interattivo
Accesso libero
Una disfagia per i cibi solidi in un ragazzo di 12 anni

L. Travan, P. Salierno, S. Martelossi

2005/7

EL Caso Clinico Interattivo
Accesso libero
Una disfagia per i cibi solidi in un ragazzo di 12 anni

L. Travan, P. Salierno, S. Martelossi

2005/7

RI Pagine elettroniche
Manifestazioni ematologiche nelle malattie mitocondriali con mutazione dell’mt-DNA

R. Cerchio, F. Timeus, P. Saracco, et al.

2005/1 — pag. 57-58

We report a 10-month-old girl who, at the age of 4 months, was admitted for increasing pallor. Severe normocytic anaemia, neutropenia and thrombocytopenia and typical diffuse vacuolization of marrow haemopoietic precursors were present. She also ...

EL Caso Clinico Interattivo
Accesso libero
Una bambina con artrite reumatoide sistemica e febbre: è una ricaduta?

C. Oretti, M. Maschio, M. Lazzerini

2004/9

EL Caso Clinico Interattivo
Accesso libero
Una bambina con artrite reumatoide sistemica e febbre: è una ricaduta?

C. Oretti, M. Maschio, M. Lazzerini

2004/9

EL Caso Clinico Interattivo
Accesso libero
Una bambina con artrite reumatoide sistemica e febbre: è una ricaduta?

C. Oretti, M. Maschio, M. Lazzerini

2004/9

EL Contributi Originali - Casi contributivi
Accesso libero
PIastrinopenia isolata x-linked da mutazione missense del gene Wasp: descrizione di un caso

C Locatelli, C Malaventura, R Ciambra, M Pocecco, L. D Notarangelo, L. D Notarangelo

2004/7

RI Pagine elettroniche
Piastrinopenia isolata X-linked da mutazione del gene WASP

2004/7 — pag. 450-450

Wiskott-Aldrich (WAS) and X-linked thrombocytopenia (XLT) are two disorders caused by different mutations of the gene WASP. WAS is characterized by recurrent infections, eczema, thrombocytopenia with low mean platet volume (MPV) and increased sus...

RI I casi del dottor Massei
L’esantema acrolocalizzato di Gianotti-Crosti

F. Massei, L. Gori

2004/5 — pag. 310-313

RI Problemi non correnti
Sette lattanti rossi: dalla dermatite atopica ai difetti congeniti dell’immunità

E. Zamuner, A. Tommasini

2003/8 — pag. 512-516

Seven infants with severe dermatitis, diarrhoea and/or infections are described. A primary immunodeficiency (PID) was considered among the diagnostic hypotheses in all cases. Thrombocytopenia, hypereosinophilia, lymphopenia and Ig deficiencies were...

RI ABC
Nuove malattie: la SARS

M. Lazzerini

2003/5 — pag. 319-322

RI Focus
Che cosa deve sapere il pediatra delle malattie rare

A. Ventura, A. Gagliardo, I. Berti, F. Marchetti

2003/5 — pag. 292

Rare diseases constitute a highly eterogeneous category of (mainly genetic) disorders. Even if the individual diseases are rare, due to their global incidence, rare diseases represent both an important cause of morbidity and mortality and a challen...

RI Focus
Accesso libero
Colestasi nella mononucleosi infettiva da virus di Epstein-Barr

F. Massei, G. Palla, C. Ughi, et al.

2002/5 — pag. 308-310

Although biochemical evidence of liver damage is frequent in children with EBV infectious mononucleosis, signs or symptoms related to an impaired bile flow as jaundice or pruritus are rare. The Authors report three cases observed in a two-year peri...

RI Aggiornamento monografico
Accesso libero
Sindrome di Shwachman-Diamond: uno studio collaborativo

L. Giglio, P. Petaros, E. Neri, et al.

2002/2 — pag. 85-89

Shwachman-Diamond (SD) syndrome is a genetic disease inherited as an autosomal-recessive character, with quite variable clinical expression, course and prognosis. The mechanisms of the disease are still not well understood, but effective symptomati...

RI Pagine elettroniche
Accesso libero
Vasculite da immunocomplessi in sindrome mononucleosica trattata con amoxicillina

M. Zoppo, A. Perino, R. Balboni, P. Capalbo, P. Pistamiglio, A. Urbino, E. Rossi

2001/10 — pag. 698

Report of a case of necrotising vasculitis with circulating immunocomplexes and alterations in hemocoagulation during a mononucleosis syndrome treated with amoxicillin....

RI I casi del dottor Massei
Accesso libero
Una malattia con decorso “sotto-sopra”

F. Massei

2001/8 — pag. 543-544

RI Pagine elettroniche
Accesso libero
Variabilità clinica nella sindrome di Schwachman: esperienza del Registro Italiano

Gruppo di Pediatri e AISS (Italian Association for Schwachman Syndrome)

2001/8 — pag. 546-548

56 cases of Schwachman syndrome have been enrolled in the Italian register in order to better define the clinical spectrum. Almost all presented the hallmark of pancreatic insufficiency and hematologic cytopenia. 78% tipical and 41% atypical osseo...

RI Focus
Accesso libero
FEBBRI PERIODICHESindromi febbrili periodiche in Pediatria

A. Tommasini, E. Neri

2001/4 — pag. 225-238

A literature review is presented covering the recent advances regarding molecular bases and clinical features of recurrent febrile syndromes in childhood. These include hypoimmune (cyclic neutropenia, benign neutropenia) and hyperimmune (mediterran...

RI Problemi correnti
Accesso libero
Trattare la mononucleosi?

M. Fontana

2000/6 — pag. 365-366

Symptoms are usually mild in young children, but in older children and adolescents systemic and pharingeal complains can be more severe, sometimes with significant airway obstruction. Only supportive care is usually recommended. This paper reports ...

EL Protocolli in pediatria ambulatoriale
Accesso libero
Le linfoadenopatie

M. Rabusin

2000/4

EL Contributi Originali - Casi contributivi
Accesso libero
Broncopolmonite con complicanze suppurative come esordio di CGD

R. Rabuano, M. Falato, F. Sellitto

2000/3

RI Pagina verde
Accesso libero
Broncopolmonite con complicanze suppurative come esordio di CGD

R.G. Rabuano, M.E. Falato, F. Sellitto

2000/3 — pag. 191-192

RI Pagina verde
Accesso libero
Anafilassi per alimenti. epidemiologia, storia naturale, challenge.risultati preliminari

G. Longo, S. Saletta

1998/9 — pag. 581

RI Pagina verde
Accesso libero
Una splenomegalia febbrile con neutropenia

P. Tamaro, C. Malorgio

1998/9 — pag. 581

RI Problemi non correnti
Accesso libero
Eritroblastopenia transitoria del bambino

F. Massei, M. Nardi, C. Favre e coll.

1998/4 — pag. 247-250

The Authors describe the diagnostic, therapeutical and prognostic features of transient erythroblastopenia of childhood (TEC) and report 5 cases. This disorder usually occurs in children aged between 6 mounts and 5 years. The clinical picture is...

RI Aggiornamento monografico
Accesso libero
Malattia granulomatosa cronica: una diagnosi che può sfuggire

C. Pignata, L. Balducci, M. Bardare e coll.

1998/3 — pag. 155-160

This is a comprehensive review article aimed at providing to paediatricians the basic knowledge on CGD and at improving the quality of care of patients affected by this rare disorder of cellular immune response. Since early diagnosis is very imp...

RI Perché si sbaglia
Accesso libero
La figlia del professore

C. Apicella

1997/9 — pag. 589-590

RI ABC
Accesso libero
Mononucleosi infettiva: immunologia, diagnosi e storia naturale dell’infezione da EBV

A. Mendoza, F. Panizon

1997/8 — pag. 502-504

RI Casi indimenticabili
Accesso libero
Un asma che non risponde al cortisone

M.T. Calipa, M. Pocecco

1997/7 — pag. 455-459