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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Neutropenia

35 articoli — 1997-2026

EL Caso contributivo
Lesioni cutanee atipiche nel lattante: quando approfondire?

Iannicelli A, Giagnuolo G, Tessitore M, Uva A, Martemucci L, Menna G

2026/2 — pag. 35-37 — DOI

Complicated and recurrent skin lesions in childhood should raise suspicion of neutropenia and prompt immuno-haematological evaluation. Through the case of an infant with recurrent dermatitis and suppurative skin infections associated with severe neut...

RI Se la conosci la riconosci
La sindrome di Barth

Dobbiani G, Crapanzano C, Tovaglieri N.

2025/10 — pag. 654-657 — DOI

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 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 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...

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 I Poster degli specializzandi
Accesso libero
Il binomio rivelatore: neutropenia e reticolo venoso marcato

G. Zanella

2018/7

RI Pagine elettroniche
Due zoppie per due diagnosi

F. Corrias

2017/7 — pag. 465-466

RI Aggiornamento
La leucemia ridotta all’osso: fatti e misfatti

A.G. Grasso, C. Radice, F. Corrias, F. Verzegnassi, F. Marchetti

2017/7 — pag. 428-434

Acute Lymphoblastic Leukaemia (ALL) is the most common cancer disease in paediatric age. Even though in the last decade there has been a steady improve of the chances of survival from this disease, it is relatively uncommon in the life of a general...

EL I Poster degli specializzandi
Accesso libero
Due zoppie per due diagnosi

F. Corrias

2017/7

EL I Poster degli specializzandi
Accesso libero
Mi fa male la schiena

S. Amoroso

2017/5

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...

EL I Poster degli specializzandi
Accesso libero
Un bimbo che cresce poco: pensa alla sindrome di Shwachman-Diamond

M. Luzzati

2016/9

EL Caso contributivo
“Storia di P”: ectima gangrenoso da Pseudomonas aeruginosa

F. Lombardi, I. Neri, E. Mazzoni, R. Francavilla, A. Lambertini

2016/6

EL I Poster degli specializzandi
Accesso libero
Ectima gangrenoso in corso di sepsi neonatale da Pseudomonas aeruginosa

E. Bottosso, L. Lucaccioni, C. Cano, B. Mordini, L. Iughetti, M. A. Bianchini, P. Repetto

2012/4

EL Casi indimenticabili
Una comunicazione difficile e una diagnosi scritta in cinese

C. Landini, E. Mazzoni, A. Lambertini

2010/3

EL Casi indimenticabili
La leucemia “italo-cinese”

C. Landini, E. Mazzoni

2009/9

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...

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 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
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 ...

RI Pagine elettroniche
Accesso libero
Meningoencefalite da Listeria in oncologia pediatrica

2002/7 — pag. 460-460

Report on two cases of Listeria-induced meningoencephalitis in a child aged 19 months with pre-B lymphatic leukemia, slightly neutropenic, and a child aged 15 years with T lymphatic leukemia, not neutropenic but lymphopenic. The disease rapidly ev...

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
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...

EL Contributi Originali - Casi contributivi
Accesso libero
Una splenomegalia febbrile con neutropenia

C. Malorgio

1998/9

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...