Large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings

被引：2

作者：

Harrison, Jonathan S. ^{[1
,2
]}

Parmar, Harsh ^{[1
,2
]}

Wang, Xiangbing D. ^{[3
]}

机构：

[1] Univ Connecticut, Sch Med, Dept Med, Farmington, CT USA

[2] Univ Connecticut, Sch Med, Carole & Ray Neag Canc Ctr, Farmington, CT USA

[3] Rutgers Robert Wood Johnson Med Sch, Dept Med, New Brunswick, NJ USA

来源：

CLINICAL CASE REPORTS | 2018年 / 6卷 / 05期

关键词：

Autoimmune polyglandular syndrome; large granular lymphocytic leukemia; pure red cell aplasia;

D O I：

10.1002/ccr3.1454

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Autoimmune polyglandular syndrome type 1 (APS1) is a rare autosomal recessive disorder, and large granular lymphocytic leukemia (LGLL) may, even more rarely, complicate APS1. LGLL may be subtle in presentation, but it is imperative to recognize LGLL in APS1 promptly, as outcome may otherwise be fatal, as described herein.

引用

页码：847 / 850

页数：4

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