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

83 articoli — 1998-2025

EL Casi indimenticabili
Splenomegalia e malattia di Gaucher

Piccioni A, Santoro L, Bruschi B, Lionetti ME, Pugliese F

2025/7 — pag. 187-187 — DOI

A 4-year-old girl, asymptomatic and in good general health, is referred to a paediatric Haemato-Oncology centre for splenomegaly associated with mild anaemia and thrombocytopenia. Initial suspicion of leukaemia is ruled out after thorough clinical, l...

RI Casi contributivi
Anemia e desaturazione… uno strano caso di favismo

Sarno E, Fabbri E, Saia RE, Pericoli R.

2025/6 — pag. 397-398 — DOI

Methaemoglobinaemia is a rare but significant complication in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency. In these individuals, oxidative stress - triggered by infections, drugs, or foods like fava beans - may convert haemoglob...

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...

EL I Poster degli specializzandi
Accesso libero
Lupus eritematoso sistemico a esordio con embolia polmonare

La Cognata D, Ferrigno M, Nannola C, La Loggia N, Di Nora A, Smilari P, Timpanaro T

2025/2 — pag. 55-56 — DOI

A 15-year-old girl was hospitalized with persistent fever lasting 40 days, accompanied by fatigue, loss of appetite and muscle pain. After initial antibiotic treatment proved ineffective, further investigations revealed pulmonary embolism and cardiac...

RI Casi indimenticabili
Monoartrite: artrite idiopatica giovanile o malattia reumatica?

Barachino A.

2024/10 — pag. 660 — DOI

A 9-year-old child presents to the emergency room with fever, pain, and swelling in the right knee. Based on the tests, the onset of pauciarticular rheumatoid arthritis is hypothesized. After further medical history assessment and a cardiology consul...

EL I Poster degli specializzandi
Accesso libero
Una trombocitopenia associata alla scabbia in un neonato: caso clinico e revisione della letteratura

Giulia La Malfa

2024/10 — pag. 220-222 — DOI

The paper presents the case of a 1-month-old infant with persistent skin lesions who was diagnosed with scabies after initial ineffective treatments. The condition was linked to thrombocytopenia and anaemia, which resolved following dermatologic ther...

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...

RI Casi indimenticabili
Anemia: sintomo o malattia?

Pentimalli E.

2024/1 — pag. 50-53 — DOI

The author describes an intriguing case finally diagnosed with ulcerative colitis in a 20-month-old boy presenting with severe anaemia....

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...

EL Caso contributivo
Febbre e gengivostomatite: non è sempre solo herpes simplex

Arnaboldi S

2023/5 — pag. 76-77 — 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 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 I Poster degli specializzandi
Accesso libero
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...

RI Problemi speciali
Approccio pratico al bambino “sempre stanco”

Gortani G.

2022/3 — pag. 168-172 — DOI

Fatigue is a common, nonspecific symptom with many different aetiologies. The term “fatigue” can be used to describe muscular weakness, difficulty or inability to initiate activity (subjective sense of weakness), reduced capacity to maintain activity...

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 Pagine elettroniche
Accesso libero
Una “crisi” celiaca

Lenhardt A, Salierno P, Calipa MT, Milocco C, Saletta S, Giglia D, Petaros P, Pascolo P, Dragovic D

2021/8 — pag. 529-532 — DOI

The authors present the case of a 3-year-old child with severe diarrhoea, hypoalbuminaemia, hypogammaglobulinaemia and anaemia eventually diagnosed as coeliac. The clinical features of the so-called coeliac crisis are discussed....

EL Casi indimenticabili
Trauma toracico e... lacerazione epatica

Parpanesi M

2021/3 — pag. 84-84 — DOI

EL Caso contributivo
Anemia normocitica e dosaggio degli ormoni tiroidei

E. Ferretti, C.M. Pini, L. Luti

2020/9 — pag. 228-230 — DOI

The paper describes the case of an 11-year-old girl presenting with normocytic hyporegenerative anaemia associated with increase of transaminases, CK and LDH. On physical exam skin pallor, mask-like facies and dry skin were observed; weight and heigh...

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 Casi indimenticabili
Una tumefazione testicolare con linfoma

I. Cattapan, I. Tosetto, A. Meneghel, M. Bellettato

2020/2 — pag. 31-32

EL I Poster degli specializzandi
Accesso libero
Zoppia, citopenia e VES: pensa anche al neuroblastoma

S. Andrade

2019/10 — pag. 250-250

RI Casi indimenticabili
Pile

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

2018/10 — pag. 662-663

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...

RI Pagine elettroniche
Morbo di Crohn: 3 casi per 3 sottolineature

P. Pascolo, M. Bramuzzo, A. Ventura

2018/5 — pag. 331-334

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 monoge...

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
Scorbuto 2017 attraverso i casi

E. Conversano, R. Bergamaschi, G. Ingrasciotta, A. Martoni, S. Monti, M. Cattalini

2017/6 — pag. 365-370

Scurvy is an uncommon presentation of vitamin deficiency that in our century is becoming more and more common, especially in patients with cognitive disorder. Being an uncommon disease, diagnosis is often delayed and can lead to unnecessary complex...

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...

RI Pagine elettroniche
Ipoglicemia chetotica e malattia celiaca: quale relazione? Descrizione di un caso clinico

M. Mainetti, V. Graziani, M. Cozzolino, F. Marchetti

2017/2 — pag. 123-124

Ketotic hypoglycaemia is the most common cause of hy-poglycaemia in preschoolers. The literature does not describe cases that have demonstrated the association between celiac disease and idiopathic ketotic hypoglycaemia. The article reports the case ...

RI Pagine elettroniche
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 — pag. 665-666

The paper describes the case of a 13-year-old boy who arrived to the emergency room for 2 syncopal episodes associated with abdominal pain. Blood tests showed Hb 10.5 g/dl with normal MCV. His general medical conditions were regular except for a ...

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

RI Percorsi clinici
La medicina “magica” che ti rimette in piedi

G.I. Baroncelli, G. Laccetta, A. Giannoni, F. Massei

2016/7 — pag. 445-448

Prolonged and exclusive breastfeeding without vitamin D supplements is a main determinant of vitamin D deficiency rickets in children of immigrants living in Italy. Dark skin may be an adjunctive factor for the development of rickets. Early signs a...

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 ...

RI Problemi correnti
La carenza di ferro nel neonato pretermine

V. Guastalla, M.C. Pellegrin, F. Rovere, R. Davanzo

2015/5 — pag. 298-305

Iron deficiency is the most common micronutrient deficiency worldwide. Preterm infants are a special risk group, because of lower total body iron at birth, rapid catch-up growth and uncompensated phlebotomy losses. Recent scientific literature sugg...

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

RI Casi indimenticabili
Dalla tiroide al duodeno: andata e ritorno

V. Moressa, L. Materazzo, N. Giurici, G. Tornese

2011/8 — pag. 534

RI Casi indimenticabili
… Tanto ti “frega” comunque!

G. Paloni, E. Rossetto

2011/8 — pag. 534

RI Focus
Il laboratorio africano essenziale

M. Fortini

2011/7 — pag. 427-441

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

RI Percorsi clinici
Un percorso troppo breve

Antonio Pulella, Rocco Cavaliere, Angela Tisci, Marco Rabusin

2008/5 — pag. 319-321

A 10-year-old girl was admitted with a 3-month history of pain in her knee joints. The pain had been occasional, very short, particularly prominent at night, when she woke up and then fell asleep again. The knee joints were warm, but there was no li...

RI Medicina, Società e Ambiente
Malattie da altitudine

G. Bartolozzi

2008/4 — pag. 239-243

Children less than one year old can be taken to altitudes up to 2,500 meters, like adults with minor or medium severity heart and lung conditions. Higher altitudes can cause severe reactions, including acute mountain sickness and pulmonary and cere...

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

RI Rubrica iconografica
Una ragazza con pelle scura e macchie scure

A. Franzil, A. Taddio, A. Saccari, L. Lepore

2005/4 — pag. 251-252

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 Pagine elettroniche
Quando una sepsi neonatale nasconde una malattia metabolica

C. Forino, C. Rodriguez-Perez

2005/1 — pag. 58-58

A 50-day-old boy presented with failure to thrive, hypotonia, pustular lesions and facial erythema, neutropenia and multiple positive cultures to Staphylococcus aureus. He was treated with intravenous antibiotics without clinical benefit. He devel...

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...

RI Casi indimenticabili
La storia di Fabio

A. Pinti

2003/3 — pag. 193-195

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 Pagine elettroniche
Accesso libero
Malaria: diagnosi tempestiva

2002/9 — pag. 606-606

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

RI Aggiornamento monografico
Accesso libero
Le microcitosi nel bambino: classificazione e approccio diagnostico

A. Sciotto, V. Furia, S.E. Munda

2001/2 — pag. 87-93

The Authors provide an overview of microcytic anemias. Causes of microcytic anemia include a wide variety of diseases, the most common being iron-deficiency, impaired haemoglobin synthesis, sideroblastic anemias and anemias due to chronic disease. ...

RI Focus
Accesso libero
CELIACHIA: DAL BAMBINO ALL’ADULTOCeliachia, autoimmunità e altro: sei famiglie e una lettera

A. Ventura, P. Petaros, T. Gerarduzzi, G. Torre, S. Martelossi, M. Persic

2000/1 — pag. 19-30

Six families are described where more than one component was diagnosed as coeliac. The reported cases provide strong evidence of both the genetic background and the broad clinical spectrum of gluten intolerance. Most cases did not show any gastroin...

RI Focus
Accesso libero
La malttia infiammatoria cronica intestinale: una esperienza “tutta d’un fiato”

G. Palla e coll.

1998/8 — pag. 523-527

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...