hemolysis

Emoglobinuria parossistica a frigore: è davvero così rara?

Esposto MP, Genesini S, Chinello M, Pezzella V, Bonetti E, Zaccaron A, Caddeo G, Vitale V, Guardo C, Cesaro S

2025/9 — pag. 231-235 — DOI

Paroxysmal Cold Haemoglobinuria (PCH) is considered the rarest form of autoimmune haemolytic anaemia (AIHA), although it is likely underdiagnosed. It is caused by biphasic haemolysins, known as Donath-Landsteiner antibodies, which bind to erythrocyte...

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...

Le colelitiasi a origine ematologica

Fantasia M, Faraguna MC, Ferrari GM, Corti P.

2024/3 — pag. 187 — DOI

A 7-year-old girl presenting with acute abdominal pain due to gallstones was eventually diagnosed with spherocytosis....

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...

Ittero, pallore e urine scure: e se fosse un’anemia emolitica autoimmune?

Tessitore A, Putoto E, Romano F, Verzegnassi F, Barbi E, Cozzi G, Parodi E.

2022/7 — pag. 451-455 — DOI

The haemolytic crisis is a sudden reduction in the half-life of red blood cells. Consequently, it leads to massive destruction of red blood cells (haemolysis), which is more significant than the compensatory capacity of the bone marrow and results in...

Calcolosi biliare: non solo per adulti...

G. Rossi, F. Cirillo, M. Sciveres, S. Riva, C. Ricotta, M. Spada, G. Maggiore

2015/8 — pag. 495-503

In recent years cholelithiasis has been on the rise among infants and children, partly because of improved diagnostic modalities, but also because of an increased awareness of emerging comorbidities, such as childhood obesity, and other associated ...

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 ...

Alloimmunizzazione post-trasfusionale: terapia immunosoppressiva con rituximab e steroidi in una bambina affetta da drepanocitosi

E. Brivio, A. Cattoni, M. Pasetti

2014/9

Quando l’EBV arriva al fegato

Sara Lega, Martina Tubaro

2014/6

Una trasfusione “di troppo”

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

2013/10

Il deficit di glucosio-6-fosfato deidrogenasi

M. Bramuzzo, S. Lega, I. Bruno

2011/10 — pag. 648-652

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked inherited disorder and it is the most common enzymatic defect in the world. G6PD is an enzyme involved in the genesis of NADPH which preserves the cells from oxidative stress. G6PD de...

ß-talassemia (Parte prima)

G. Bartolozzi

2006/1

Un caso di malaria da Plasmodium Falciparum

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

2005/5

Iperbilirubinemia neonatale

2001/4