Congenital hepatic fibrosis: a very uncommon cause of pancytopenia in children.

Vito Di Marco, Paolo D'Angelo, Vincenzo Benigno, Maurizio Aricò, Antonino Trizzino, Piero Farruggia, Delia Russo, Serena Tropia, Giuseppe Tarantino, Pier Luigi D'Angelo

Risultato della ricerca: Article

2 Citazioni (Scopus)

Abstract

The disease presentation of autosomal recessive polycystic kidney disease (OMIM #263200, ARPKD) is highly variable and includes polycystic kidneys, pulmonary hypoplasia, and congenital hepatic fibrosis. The authors report an unusual case of ARPKD presenting with hepatosplenornegaly and cytopenia mimicking acute leukemia
Lingua originaleEnglish
pagine (da-a)567-568
Numero di pagine2
RivistaJOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
Volume27
Stato di pubblicazionePublished - 2005

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All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Hematology
  • Oncology

Cita questo

Di Marco, V., D'Angelo, P., Benigno, V., Aricò, M., Trizzino, A., Farruggia, P., Russo, D., Tropia, S., Tarantino, G., & D'Angelo, P. L. (2005). Congenital hepatic fibrosis: a very uncommon cause of pancytopenia in children. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 27, 567-568.