原发性干燥综合征老年男性患者的顺序性免疫性血小板减少症(ITP)和血栓性血小板减少性紫癜(TTP):当有疑问时,使用血浆评分。

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Case Reports in Medicine Pub Date : 2021-11-30 eCollection Date: 2021-01-01 DOI:10.1155/2021/6869342
Devon D Miller, Joseph A Krenzer, Vaishalee P Kenkre, William Nicholas Rose
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引用次数: 7

摘要

摘要:血栓性血小板减少性紫癜(TTP)是一种罕见的、危及生命的血栓性微血管疾病,由获得性ADAMTS13自身抗体引起,需要精品化治疗,紧急血浆置换。因此,TTP通常被称为“不能错过”的诊断。病例:我们报告了一名TTP患者,他有免疫性血小板减少症(ITP)的病史,TTP的非典型人口统计学特征,也符合原发性干燥综合征的标准。这一极其罕见的组合很容易让人将TTP视为一种诊断。讨论。我们的病例进一步证明了使用PLASMIC评分作为一种工具的实际效用,即使患者具有统计学上罕见的特征,也可以帮助识别TTP患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Sequential Immune Thrombocytopenia (ITP) and Thrombotic Thrombocytopenic Purpura (TTP) in an Elderly Male Patient with Primary Sjogren's Syndrome: When in Doubt, Use the PLASMIC Score.

Introduction: Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening thrombotic microangiopathy due to an acquired autoantibody to ADAMTS13 that requires a boutique treatment, urgent plasma exchange. Thus, TTP is often termed a "cannot miss" diagnosis.

Case: We report a patient with TTP who had a history of immune thrombocytopenia (ITP), had atypical demographics for TTP, and had also met criteria for primary Sjogren's syndrome. This exceedingly rare combination presented a temptation to dismiss TTP as a diagnosis. Discussion. Our case further demonstrates the practical utility of using the PLASMIC score as a tool that can help identify patients with TTP even when the patient has statistically rare characteristics.

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来源期刊
Case Reports in Medicine
Case Reports in Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
0.00%
发文量
53
审稿时长
13 weeks
期刊最新文献
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