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唐氏综合征巨核母细胞白血病样反应伴围生期内脏纤维化。

Perinatal visceral fibrosis accompanying the megakaryoblastic leukemoid reaction of Down syndrome.

作者信息

Becroft D M, Zwi L J

机构信息

Princess Mary Laboratory, Auckland Hospital, New Zealand.

出版信息

Pediatr Pathol. 1990;10(3):397-406. doi: 10.3109/15513819009067127.

Abstract

Two infants with Down syndrome, one 4 weeks old and the other stillborn, at necropsy showed hepatic and pancreatic fibrosis, which was very severe in the liver of the liveborn infant and in the pancreas of the stillbirth. The liveborn infant had typical hematological features of the transient congenital leukemoid reaction of Down syndrome, and the identification of a megakaryoblastic component was consistent with recent opinion that this is a spontaneously-remitting congenital megakaryoblastic leukemia. The hydropic stillborn infant had intense extramedullary megakaryocytosis. The visceral fibrosis may have had a pathogenesis similar to that postulated for the myelofibrosis of megakaryoblastic leukemia in older children.

摘要

两名唐氏综合征患儿,一名4周大,另一名为死产儿,尸检显示肝脏和胰腺纤维化,在活产儿的肝脏和死产儿的胰腺中纤维化非常严重。活产儿具有唐氏综合征短暂先天性类白血病反应的典型血液学特征,巨核母细胞成分的鉴定与最近的观点一致,即这是一种自发缓解的先天性巨核母细胞白血病。水肿的死产儿有强烈的髓外巨核细胞增多。内脏纤维化的发病机制可能与大龄儿童巨核母细胞白血病的骨髓纤维化的发病机制相似。

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