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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Haemophagocytic lymphohistiocytosis

5 articoli — 2012-2022

RI Percorsi clinici
Quando la linfoistiocitosi emofagocitica è secondaria

Ventresca S, Fabbri E, Bracaglia C, Gasperini P, Filippini B, Libertucci F, Bigucci B, Pericoli R, Vergine G.

2022/2 — pag. 97-102 — DOI

The paper describes the case of a 1-year-old Caucasian boy with a 1-month history of fever and splenomegaly. Laboratory findings showed pancytopenia, hypertriglyceridemia and hyperferritinemia. Secondary haemophagocytic lymphohistiocytosis was suspec...

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...

RI Aggiornamento
Accesso libero
Covid-19 e risposta immune

S. Volpi, S. Naviglio, A. Tommasini

2020/4 — pag. 223-231

Covid-19 outbreak is about to reach the peak of infected people in Italy. Huge amount of data is being published on this epidemic in all medical journals, with especial concern on severe cases. Unfortunately, most reports are just descriptive and onl...

RI Percorsi clinici
L’EBV che non mi aspetto: MASe ci penso...!

A. Di Mascio, C. Redice, S. Pusceddu, V. Camelli, F. Marchetti

2016/10 — pag. 637-640

The paper reports the case of a 14-year-old boy who presented to our attention because for three days he had fever, laterocervical lymphadenopathy with limited movements of the neck and cytopoenia. The clinical diagnostic process led to the diagnos...

RI Aggiornamento
Linfoistiocitosi emofagocitica: una sfida diagnostica per il pediatra

E. Sieni, V. Cetica, M. Aricò

2012/1 — pag. 21-29

Haemophagocytic lymphohistiocytosis (HLH) is a severe hyperinflammatory syndrome caused by uncontrolled but ineffective immune response. Inherited human disorders causing the defect of selected proteins involved in the cellular cytotoxicity machinery...

Argomenti correlati
COVID-19 (133) Children (127) Pneumonia (114) Diagnosis (83) Mutation (62) Splenomegaly (54) polmonite (50) SARS-CoV-2 (50) Epstein-Barr Virus (41) Prenatal Diagnosis (40) Herpesvirus 4, Human (38) Pancytopenia (36) Neutropenia (35) Bone Marrow Examination (31) Immunity, Innate (25) Inflammation (23) Lymphohistiocytosis, Hemophagocytic (21) Apoptosis (20) Hematopoietic Stem Cell Transplantation (19) Genetic Counseling (19)