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Pleuropulmonary blastoma in a child with autosomal‐recessive polycystic kidney disease

✍ Scribed by Jeffrey Traubici; Gino R. Somers; Simon C. Ling; Rachel J. Pearl; Paul C. Nathan

Publisher
Springer-Verlag
Year
2011
Tongue
English
Weight
366 KB
Volume
41
Category
Article
ISSN
0301-0449

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## Communicated by Jurgen Horst Autosomal recessive polycystic kidney disease (ARPKD) is an important cause of childhood renal-and liverrelated morbidity and mortality. The clinical spectrum is widely variable. About 30 to 50% of affected individuals die in the neonatal period, while others survive