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结节病继发免疫性血小板减少性紫癜

Immune Thrombocytopenic Purpura Secondary to Sarcoidosis.

作者信息

Barlas Aisha, Ramachandran Lintu

机构信息

Department of Internal Medicine, Javon Bea Hospital, Rockford, USA.

出版信息

Maedica (Bucur). 2022 Mar;17(1):234-236. doi: 10.26574/maedica.2022.17.1.234.

Abstract

Sarcoidosis is a systemic granulomatous disease involving multiple organs with predominantly pulmonary manifestations. Severe thrombocytopenia is a relatively rare hematologic manifestation of sarcoidosis. Immune thrombocytopenia is usually characterized by excessive antibody production leading to platelet destruction. There are a few reported cases of immune thrombocytopenic purpura secondary to sarcoidosis, but the pathophysiologic mechanism remains unknown. We report the case of a 65-year-old woman who presented severe thrombocytopenia and was found to have immune thrombocytopenic purpura secondary to sarcoidosis.

摘要

结节病是一种累及多个器官的全身性肉芽肿性疾病,主要表现为肺部症状。严重血小板减少是结节病相对罕见的血液学表现。免疫性血小板减少通常表现为抗体过度产生导致血小板破坏。有少数关于结节病继发免疫性血小板减少性紫癜的病例报道,但病理生理机制仍不清楚。我们报告一例65岁女性患者,该患者出现严重血小板减少,被发现患有结节病继发免疫性血小板减少性紫癜。

相似文献

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Immune Thrombocytopenic Purpura Secondary to Sarcoidosis.结节病继发免疫性血小板减少性紫癜
Maedica (Bucur). 2022 Mar;17(1):234-236. doi: 10.26574/maedica.2022.17.1.234.
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本文引用的文献

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Immune thrombocytopenic purpura secondary to .继发于……的免疫性血小板减少性紫癜
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South Med J. 1992 Jul;85(7):775-8. doi: 10.1097/00007611-199207000-00028.

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