Henoch-Schönlein purpura with epididymo-orchitis: A rare extra-cutaneous manifestation

IF 0.5 Q4 UROLOGY & NEPHROLOGY
Majd Oweidat , Islam H. Karajeh , Widad Abu Mayyala , Mohammed Alra'e , Ammar Y. Hmidat
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引用次数: 0

Abstract

Henoch-Schönlein Purpura (HSP), or IgA vasculitis, is a systemic inflammatory disorder primarily affecting children. While common symptoms include purpura, abdominal pain, and arthritis, testicular involvement is rare. We report a case of a young boy presenting with severe scrotal pain and swelling, later identified as epididymo-orchitis secondary to HSP. Diagnosis was confirmed via Doppler ultrasound, and treatment with corticosteroids and antibiotics resulted in rapid symptom resolution. This case highlights the importance of recognizing rare extra-cutaneous manifestations of HSP and underscores the need for prompt diagnosis and tailored management to achieve favorable outcomes.
Henoch-Schönlein伴有附睾睾丸炎的紫癜:一种罕见的皮肤外表现。
Henoch-Schönlein紫癜(HSP),或IgA血管炎,是一种主要影响儿童的系统性炎症性疾病。虽然常见的症状包括紫癜、腹痛和关节炎,但很少累及睾丸。我们报告一个病例的年轻男孩提出严重的阴囊疼痛和肿胀,后来确定为附睾睾丸炎继发于HSP。经多普勒超声确诊,经皮质类固醇和抗生素治疗后症状迅速缓解。该病例强调了认识罕见的皮肤外表现的重要性,并强调了及时诊断和量身定制治疗的必要性,以获得良好的结果。
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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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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