白细胞破坏性血管炎伪装成慢性特发性血小板减少性紫癜。

Saria Tasnim, Hina Yousuf, Yasir Al-Hilli, Waqas Rasheed, Kaylee Shepherd
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引用次数: 0

摘要

背景:特发性血小板减少性紫癜和白细胞破坏性血管炎可以以相似的方式出现,并且在临床上很难区分,除非进行活检。这可能导致诊断困境和管理延误。建议进行彻底的评估以确定病因,尽管约有一半是特发性的。病例介绍:患者79岁,长期血小板减少继发于慢性特发性血小板减少性紫癜,表现为皮疹。虽然它被认为是继发于特发性血小板减少性紫癜,但活检显示存在白细胞破坏性血管炎。结论:虽然大多数白细胞破裂性血管炎病例是轻微的,无需干预即可消退,但许多病例由于活检延误而未被诊断。卫生保健专业人员应该确定并治疗潜在的原因。
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Leukocytoclastic Vasculitis Masquerading as Chronic Idiopathic Thrombocytopenic Purpura.

Background: Idiopathic thrombocytopenic purpura and leukocytoclastic vasculitis can present in a similar fashion and can be very hard to differentiate clinically without a biopsy. This can cause diagnostic dilemma and delay in management. A thorough evaluation is recommended to determine etiology, although about half are idiopathic.

Case presentation: A patient aged 79 years with longstanding thrombocytopenia secondary to chronic idiopathic thrombocytopenic purpura presented with a rash. Although it was thought to be secondary to idiopathic thrombocytopenic purpura, a biopsy revealed presence of leukocytoclastic vasculitis.

Conclusions: Although most leukocytoclastic vasculitis cases are mild and resolve without intervention, many go undiagnosed due to biopsy delays. Health care professionals should determine and treat the underlying cause.

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