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伴有红细胞再生障碍的自身免疫性淋巴增殖综合征

Autoimmune Lymphoproliferative Syndrome with Red Cell Aplasia.

作者信息

Meena K R, Bisht Supriya, Tamaria K C

机构信息

Department of Pediatrics, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, 110029, India.

出版信息

Indian J Pediatr. 2015 Dec;82(12):1172-4. doi: 10.1007/s12098-015-1779-2. Epub 2015 May 15.

Abstract

Autoimmune Lymphoproliferative Syndrome (ALPS) is a rare inherited disorder of abnormal lymphocyte apoptosis, leading to chronic lymphoproliferation. It presents as lymphadenopathy, hepatosplenomegaly and autoimmune phenomena. Pure red cell aplasia is characterized by normochromic normocytic anemia, reticulocytopenia, and absence of erythroblasts from a normal bone marrow. Only few lymphoproliferative disorders have been associated with erythroid aplasia. The authors are reporting a case of ALPS associated with red cell aplasia in a 7-y-old girl.

摘要

自身免疫性淋巴细胞增生综合征(ALPS)是一种罕见的遗传性疾病,其特征为淋巴细胞凋亡异常,导致慢性淋巴细胞增生。临床表现为淋巴结病、肝脾肿大和自身免疫现象。纯红细胞再生障碍性贫血的特点是正色素正细胞性贫血、网织红细胞减少,且正常骨髓中无成红细胞。仅有少数淋巴细胞增生性疾病与红细胞再生障碍有关。本文作者报告了一例7岁女童患ALPS并伴有红细胞再生障碍的病例。

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