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

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

Promozione della Salute, Materno-Infantile, di Medicina Interna e Specialistica di Eccellenza “G. D’Alessandro”

Risultato della ricerca: Article › peer review

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 originale	English
pagine (da-a)	567-568
Numero di pagine	2
Rivista	JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
Volume	27
Stato di pubblicazione	Published - 2005

All Science Journal Classification (ASJC) codes

Pediatrics, Perinatology, and Child Health
Hematology
Oncology

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Congenital hepatic fibrosis: a very uncommon cause of pancytopenia in children. / Di Marco, Vito; D'Angelo, Paolo; Benigno, Vincenzo; Aricò, Maurizio; Trizzino, Antonino; Farruggia, Piero; Russo, Delia; Tropia, Serena; Tarantino, Giuseppe; D'Angelo, Pier Luigi.

In: JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, Vol. 27, 2005, pag. 567-568.

Risultato della ricerca: Article › peer review

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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",

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T1 - Congenital hepatic fibrosis: a very uncommon cause of pancytopenia in children.

AU - Di Marco, Vito

AU - D'Angelo, Paolo

AU - Benigno, Vincenzo

AU - Aricò, Maurizio

AU - Trizzino, Antonino

AU - Farruggia, Piero

AU - Russo, Delia

AU - Tropia, Serena

AU - Tarantino, Giuseppe

AU - D'Angelo, Pier Luigi

PY - 2005

Y1 - 2005

N2 - 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

AB - 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

UR - http://hdl.handle.net/10447/13857

M3 - Article

VL - 27

SP - 567

EP - 568

JO - Journal of Pediatric Hematology/Oncology

JF - Journal of Pediatric Hematology/Oncology

SN - 1077-4114

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