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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Anemia

48 articoli — 1998-2025

EL Caso contributivo
"Che cosa può celarsi dietro un'anemia...": un caso di atresia duodenale a esordio tardivo

Allegra M, Dolce R, Bignone L, Raso E, Caruso A, Giglione E, Putignano L, Alizzi C, Cardella F, Corsello G

2025/5 — pag. 103-106 — DOI

Duodenal atresia (AD) is a congenital malformation characterised by complete or incomplete intrinsic obstruction of the duodenum. Prenatal diagnosis is often possible. Type 1 AD, according to the Gray-Skandalakis classification, consists of transvers...

RI Pagine elettroniche
La B12 c'è ma non funziona

Vitale R.

2024/7 — pag. 468-470 — DOI

The paper reports the typical case and clinic of a defect in B12 metabolism. Such diseases, which are rare, mimic B12 intake or absorption deficits (crasis alterations, mixed neuropathy) but are distinguished first and foremost by the presence of nor...

EL Il punto su
Le parassitosi intestinali

Nuzzi G, Riboldi L, Pietravalle A, Putoto G

2023/8 — pag. 157-161 — DOI

Parasitic infections are still a major public health problem in developing countries. The paper presents the case of an 18-month-old girl taken by her mother to the paediatrics department of St. Luke’s Hospital in Wolisso, Ethiopia for general malais...

RI Aggiornamento
Il bambino con anemia severa: proposta di gestione diagnostico-terapeutica

Muratore E, Ruggi A, Abram N, Zanaroli A, Pierantoni L, Lanari M, Zama D.

2023/3 — pag. 159-168 — DOI

Anaemia is a common issue in the paediatric age group and it is not uncommon to encounter severe cases of anaemia in the Paediatric Emergency Unit. The correct identification of patients requiring urgent care is of central importance to provide timel...

RI Pagine elettroniche
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...

EL Caso contributivo
Anemia severa, arresto di crescita... e dintorni

Tognato E, Fiorica L, Perona A, Loperfido B, Cimminelli L, Ceratto S, Enrico G, Felici E, Manzoni P

2021/9 — pag. 277-279 — DOI

Iron deficiency is the most commonly detected nutritional disorder in childhood and at the same time the most frequent cause of anaemia worldwide. In most cases it can go unnoticed, because it causes subtle symptoms and signs. Iron plays a key role i...

EL Caso contributivo
Disturbo della condotta alimentare, ecchimosi e carenza di vitamina C

Attico A, Iacono A, Biserna L, Brandolini S, Marchetti F

2021/9 — pag. 273-276 — DOI

The paper presents the case of a 16-year-old girl with a 6-month history of eating disorder, restrictive subtype and diffuse ecchymosis. Anamnestic history and laboratory investigations allowed excluding coagulation disorders and making the diagnosis...

RI Focus
Non era una MICI

F. Graziano, R. Ganci, M. Di Pisa, et al.

2020/5 — pag. 319-320

The paper describes a case of colorectal adenocarcinoma (CRC) in a twelwe-year-old girl, at first diagnosed as IBD. CRC represents 1-2% of paediatric cancers. Generally, it occurs after the age of 10 years of life. Symptoms of presentation include ab...

EL I Poster degli specializzandi
Accesso libero
Cerchi una celiachia, trovi... una leucemia

S. Molinari

2018/6

EL Casi indimenticabili
Sbarchi

A. Filpo

2018/6

EL Caso contributivo
Un’emolisi ben mascherata

G. Del Borrello

2018/6

Chronic haemolytic anaemia is a pathophysiological process that can be the expression of many possible etiologies (e.g. a congenital defect of a membrane protein, immune-mediated destruction, enzymopathies, altered erythrocyte development). The paper...

EL Caso contributivo
Febbre persistente, dolore toracico e arterite di Takayasu

B. Filippini, B. Bigucci, F. Mascella, M. Gattorno, G. Vergine

2018/5

Takayasu’s arteritis (TA) is an extremely rare vasculitis that presents in paediatric age that typically affects adolescents. Clinical manifestations of TA are polymorph and in the fists stage of the disease systemic aspecific symptoms such as fever,...

EL Caso contributivo
Morbo di Crohn: 3 casi per 3 sottolineature

P. Pascolo, M. Bramuzzo, A. Ventura

2018/5

Crohn’s disease is an inflammatory bowel disease diagnosed in paediatric age, especially during adolescence, in approximately one third of the cases. Pathogenesis is unknown but growing evidence suggests that immunological anomalies due to monogenic ...

RI Problemi speciali
Picacismo e carenza di ferro: una relazione problematica

S. Zanella, C. Borgna-Pignatti

2017/5 — pag. 291-294

Pica is the compulsive eating of non-nutritive substances and is often associated with iron deficiency but its pathophysiology is unknown. The paper is a review of the literature based on the search of online databases that was carried out using th...

EL Caso contributivo
Emorragia splenica post-traumatica in un adolescente: il ruolo della angio-embolizzazione

P. Gallo, C. Radice, M. Mainetti, C. Renzelli, D. Palmarini, F. Marchetti

2016/10

EL Caso contributivo
Quando la sferocitosi incontra il chirurgo

C. Bibalo

2015/6

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 ...

EL Casi indimenticabili
La mia Africa

M. Bellettato

2014/5

EL Casi indimenticabili
Al di là dell’occhio!

G. Ferrara, E. Zanelli

2014/3

EL Casi indimenticabili
Una trasfusione “di troppo”

F. Sfriso, F. Visentin, G. Biddeci, T. Zangardi, S. Zanconato, S. Scanferla, S. Masiero

2013/10

RI Aggiornamento
La nuova diagnostica delle anemie microcitiche

A. Iolascon, A. Gambale, C. Tortora, M. Bruno, L. De Falco

2013/9 — pag. 563-569

Microcytic anaemia is the most common form of anaemia, characterized by reduced MCV, often associated with hypochromia of red blood cells. Among the causes of microcytic anaemia, iron deficiency anaemia is the most common. The latest scientific dis...

EL I Poster degli specializzandi
Accesso libero
Lupus in fabula

S. Venezia, M. Corradi, S. Osmi, C. Greco, N. Carano

2013/5

RI Problemi speciali
Reticolociti: un parametro poco conosciuto e troppo poco utilizzato

U. Ramenghi, G. Ansaldi, M. Davitto, A. Mondino, C. Olivieri, R. Mazzone

2012/10 — pag. 649-651

The paper describes the usefulness of reticulocyte count in the diagnosis and management of anaemia. Reticulocytes are immature red cells that do not have the nucleus, but hold residual extranuclear RNA. In traditional morphologic examination, reti...

EL Caso contributivo
Quando il dolore osseo viene… dal sangue

L. Mambelli, L. Marangio, L. Pini, I.A. Venturi, M. Poli, O. Donzelli, F. Marchetti

2012/10

The paper describes the case of an 8-year-old Moroccan girl who presented with recurrent multi-focal bone pains associated with negative flogosis indexes and standard radiological exams. The magnetic resonance exam of her thighbones showed a multi-fo...

EL Casi indimenticabili
L'importante è crederci!

E. Benelli

2012/7

EL Caso contributivo
La picnocitosi infantile: una causa rara ma non infrequente di anemia emolitica neonatale severa

A.M. Aurino, R. Di Concilio, G. d’Urzo, M. Amendolara, C. Romano, G. Attianese, S. Mauriello, C. Di Filippo, G. Amendola

2011/3

The diagnosis and treatment of six patients with infantile pyknocytosis are reported. The clinical course and the diagnostic work-up are shown. All the patients necessitated therapy: phototherapy in five patients and one red blood cell transfusion in...

EL Casi indimenticabili
Una banale gastroenterite?

A. Paladini, S. Ciccone, C. Farneti

2010/10

EL Caso contributivo
Infezioni ricorrenti nel lattante: spia di un problema più complesso?

C. Calitri, F. Mignone, C. Bertaina, C. Gabiano, C. Scolfaro

2010/10

An 11-month-old girl was referred to our Paediatric Department for immunological evaluation. She has had history of recurrent infections since birth. During different hospital admissions, blood tests revealed persistent microcytic anemia, liver funct...

RI Pagine elettroniche ; Ricerca
Screening per minori adottati o recentemente immigrati da Paesi a rischio?Un'esperienza su 100 casi

F. De Franco, F. Colonna, E. Miorin, I. Robieux, E. Moretto, P. Aragona, L. Lubrano

2010/3 — pag. 191-192

100 children were studied, 72 recently immigrated with their family from developing countries (40% from sub- Saharan Africa) and 28 adopted from foreign countries. By protocol a complete physical examination and the following tests were performed...

EL Contributi Originali - Ricerca
Accesso libero
Screening per minori adottati o recentemente immigrati da Paesi a rischio? Un’esperienza su 100 casi

F. De Franco, F. Colonna, E. Miorin, I. Robieux, E. Moretto, P. Aragona, L. Lubrano

2010/3

EL Casi indimenticabili
Quando le vitamine servono davvero

F. Lombardi, A.L. Quitadamo, A. Pelizzoni, P. Accorsi, F. Olivetti

2010/2

EL Casi indimenticabili
La leucemia “italo-cinese”

C. Landini, E. Mazzoni

2009/9

EL Contributi Originali - Casi contributivi
Accesso libero
Anemia emolitica autoimmune in un bambino di 7 anni con colite ulcerosa

C. Brondello, M. Lorusso, E. Pozzi, F. Bronzini, F. Mangiantini, M. de Martino, P. Lionetti

2007/9

RI Problemi correnti
Anemie facili e difficili

U. Ramenghi

2007/1 — pag. 27-31

Most forms of anemias in childhood are easy to diagnose. A decreased mean corpuscolar volume (MCV) is due to reduced hemoglobin synthesis and suggests iron deficiency or thalassemia. Anemia with a normal MCV is mainly due to hemolysis or hemorrhage...

EL Pediatria per l'ospedale
Accesso libero
ß-talassemia (Parte prima)

G. Bartolozzi

2006/1

RI Focus
La celiachia dal vero: dal bambino all’adulto filo conduttore è l’anemia

T. Gerarduzzi, M. Lazzerini, F. De Franco, A. Lenhardt, I. Berti

2005/7 — pag. 434-455

EL Protocolli di diagnosi e terapia
Accesso libero
La malaria

M. Lazzerini

2005/5

EL Contributi Originali - Casi contributivi
Accesso libero
Un caso di malaria da Plasmodium Falciparum

S. Vaccher, F. Patarino, M. Lazzerini, E. Barbi

2005/5

EL Contributi Originali - Casi contributivi
Accesso libero
Manifestazioni ematologiche nelle malattie mitocondriali con mutazione del mt-DNA

R. Cerchio, F. Timeus, P. Saracco, L. Garbarini, P. Quarello, M. Forni, L. Montezemolo, U. Ramenghi, M. Zeviani

2005/1

RI ABC
Leggere l’emocromo

I. Bruno

2004/2 — pag. 113-115

EL Caso Clinico Interattivo
Accesso libero
Un lattante con pianto, anemia e bassi valori di immunoglobuline

M. Lazzerini

2003/10

EL Caso Clinico Interattivo
Accesso libero
Un lattante con pianto, anemia e bassi valori di immunoglobuline

M. Lazzerini

2003/10

RI Pagine elettroniche
Un caso di istiocitosi con interessamento cutaneo ed edema

2003/8 — pag. 535

A case of histiocytosis with skin involvement, multifocal disease including visceral involvement....

RI Pagine elettroniche
Un caso di emosiderosi polmonare idiopatica

2003/6 — pag. 400

A case of idiopathic pulmonary emosiderosis with irondeficiency anemia as the only presenting sign is described...

EL Contributi Originali - Ricerca
Accesso libero
Laboratorio "fai da te" in un ospedale africano

A. Azzini, S. Facchini, F. Panizon

2003/2

EL Contributi Originali - Casi contributivi
Accesso libero
Diagnosi precoce di malaria da Plasmodium falciparum

A. Comite, A. Perrone, R. Chakrokh, P. Salvago, A. Corsini, P. Minelli, M. Malni

2002/9

RI Aggiornamento monografico
Accesso libero
La carenza di ferro Parte II: Clinica, prevenzione e terapia

C. Vullo

1998/6 — pag. 359-374

Part II of the review on iron deficiency (ID) is devoted to clinical manifestations, prevention and treatment. Pallor and fatigue are increasingly rare as presenting signs and symptoms of ID in industrialized countries. More subtle conditions su...

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...