Development of nephrotic syndrome during immunosuppressive treatment for aplastic anaemia with monosomy 7 in a 16‐year‐old boy: A case report.

Autor:	Yanagi, Masato, Kobayashi, Ryoji, Matsushima, Satoru, Hori, Daiki, Sano, Hirozumi, Yoshihara, Mayumi, Kobayashi, Kunihiko
Předmět:	APLASTIC anemia NEPHROTIC syndrome ANEMIA treatment FOCAL segmental glomerulosclerosis HEMATOPOIETIC stem cell transplantation GRAFT versus host disease
Zdroj:	Journal of Paediatrics & Child Health; Feb2023, Vol. 59 Issue 2, p365-367, 3p
Abstrakt:	Aplastic anaemia (AA) complicated by nephrotic syndrome (NS) is rare except in patients with chronic graft-versus-host disease after haematopoietic stem cell transplantation. Abrams I et al i . reported a case of 9-year-old boy, who presented pathologically proven minimal change NS, gradually progressed to concurrent idiopathic AA.[5] Prior to the diagnosis of AA, he had frequent relapses of NS. We describe a 16-year-old boy with AA and monosomy 7 who developed NS during immunosuppressive treatment for AA without haematopoietic stem cell transplantation. [Extracted from the article]
Databáze:	Complementary Index
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