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
TRIZZINO A, FARRUGGIA P, RUSSO D, D'ANGELO P, TROPIA S, BENIGNO V, et al. (2005). Congenital hepatic fibrosis: a very uncommon cause of pancytopenia in children. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 27(10), 567-568 [10.1097/01.mph.0000184577.46458.7e].
Congenital hepatic fibrosis: a very uncommon cause of pancytopenia in children.
D'ANGELO, Pier Luigi;TARANTINO, Giuseppe;DI MARCO, Vito;
2005-01-01
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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