Hepatosplenomegaly

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...

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...

"Amici per la pelle": un caso di leishmaniosi

Fantasia M, Vecchi M, Cavalleri L, Bruni F, Provenzi M

2025/4 — pag. 81-85 — DOI

Leishmaniasis is an infectious disease caused by protozoa of the Leishmania genus, parasites of humans and several domestic and wild animals, and transmitted via vectors. The authors describe the case of an 18-month-old girl, presenting to the Emerge...

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. ...

Rapida evoluzione di una istiocitosi a cellule di Langerhans cutanea isolata

Brusadelli C, Dell’Acqua F, Vendemini F, Ferrari GM, Corti P

2021/7 — pag. 197-200 — DOI

The paper reports the case of a three-month-old girl presenting with maculopapular lesions all over her scalp, trunk, axilla region and groin. One month earlier she had been diagnosed with LCH through skin biopsy for persisting maculopapular rash. No...

Sbarchi

A. Filpo

2018/6

Ipereosinofilia severa: un caso da non dimenticare

E. Santi

2017/6

Brucellosi: un raro caso di recidiva

M.C. Castiglione

2017/1

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 ...

Al di là dell’occhio!

G. Ferrara, E. Zanelli

2014/3

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...

I meriti degli altri

E. Barbi

2009/3

Un caso di bartonellosi viscerale in paziente immunocompetente

R. Grazioli, R. Milani Capialbi, F. Marchetti, A. Bettinelli

2008/6 — pag. 395-397

We report a case of a 5-year-old immunocompetent boy with persistent fever and a diffuse enlargement of laterocervical lymph nodes. We performed first an abdominal ultrasonography and then a CT showed multiple hepatosplenic abscesses. Later the f...

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...

Storie di immigrati

I. Giuseppin

2007/5

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

Un caso di malaria da Plasmodium Falciparum

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

2005/5

Ittero neonatale e malattia di Nieman-Pick tipo C

C. Martini

2000/10

Ittero neonatale e malattia di Nieman-Pick tipo C

C. Martini

2000/10 — pag. 679-680

A case of early onset Nieman-Pick type C disease, with neonatal onset of mixed hyperbilirubinemia and increased aminotransferases, and later development of hypotonia and psychomotor delay, is reported. The congenital, functional and metabolic caus...

Una splenomegalia febbrile con neutropenia

C. Malorgio

1998/9

Una splenomegalia febbrile con neutropenia

P. Tamaro, C. Malorgio

1998/9 — pag. 581