继发于……的免疫性血小板减少性紫癜
Immune thrombocytopenic purpura secondary to .
作者信息
Ramachandran Lintu, Baloch Luqman, Djirdeh Taha Mohamed, Sidhu Yadwinder, Gentile Nicole, Affinati Mario
机构信息
Department of Internal Medicine, Mercyhealth, Rockford, Illinois.
出版信息
Proc (Bayl Univ Med Cent). 2021 Sep 15;35(1):60-61. doi: 10.1080/08998280.2021.1973293. eCollection 2022.
Immune thrombocytopenic purpura is a disorder characterized by decreased platelet count that may be secondary to infectious or autoimmune etiologies. We present a patient with upper gastrointestinal bleeding complicated by severe thrombocytopenia. Endoscopy revealed gastritis with pathology positive for . Platelet count normalized after triple antibiotic therapy. The precise mechanism by which causes immune thrombocytopenic purpura remains unclear; however, there are several plausible mechanisms. This case highlights the importance of keeping in the differential in patients presenting with thrombocytopenia.
免疫性血小板减少性紫癜是一种以血小板计数减少为特征的疾病，其可能继发于感染性或自身免疫性病因。我们报告一名患有上消化道出血并伴有严重血小板减少症的患者。内镜检查显示胃炎，病理检查呈阳性。三联抗生素治疗后血小板计数恢复正常。导致免疫性血小板减少性紫癜的确切机制尚不清楚；然而，有几种合理的机制。该病例强调了在血小板减少症患者的鉴别诊断中考虑[此处原文缺失关键信息]的重要性。
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