Cutaneous leukocytoclastic vasculitis with concurrent colitis of uncertain aetiology.

IF 0.4 Q3 MEDICINE, GENERAL & INTERNAL
Vanessa Pei Xian Yaw, Mohamed Korani, Rakibul Anowar, Syed Mujtaba Hasnain Nadir
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引用次数: 0

Abstract

This case presents a female in her 20s with biopsy-confirmed cutaneous leukocytoclastic vasculitis (LCV) and significant gastrointestinal (GI) symptoms, manifesting as recurrent rectal bleeding, abdominal pain and maculopapular rash. The patient's symptoms emerged shortly after treatment with phenoxymethylpenicillin for tonsillitis. Investigations revealed left-sided colitis with distinctive endoscopic findings. Skin biopsy confirmed cutaneous LCV; however, colonic biopsies demonstrated non-specific inflammation without histological evidence of vasculitis. Therefore, GI vasculitic involvement could not be confirmed. Negative autoimmune serology excluded primary autoimmune disorders. Following treatment with prednisolone and mesalazine, the patient's symptoms resolved and she showed sustained improvement. While clinical improvement occurred after corticosteroid therapy, this response is non-specific and does not confirm GI vasculitis. Given the absence of vasculitic features on GI histology, the relationship between cutaneous LCV and colitis in this case remains associative rather than proven. This case underscores the importance of diagnostic caution when extracutaneous manifestations are suspected in LCV.

皮肤白细胞破裂性血管炎并发不明原因的结肠炎。
该病例是一名20多岁的女性,活检证实皮肤白细胞破裂性血管炎(LCV)和明显的胃肠道(GI)症状,表现为复发性直肠出血、腹痛和斑疹样皮疹。患者在使用苯氧甲基青霉素治疗扁桃体炎后不久出现症状。调查显示左侧结肠炎具有独特的内镜检查结果。皮肤活检证实皮肤LCV;然而,结肠活检显示非特异性炎症,没有血管炎的组织学证据。因此,不能确定是否累及胃肠道血管。自身免疫性血清学阴性排除原发性自身免疫性疾病。经强的松龙和美沙拉嗪治疗后,患者症状缓解,病情持续改善。虽然皮质类固醇治疗后出现了临床改善,但这种反应是非特异性的,不能证实是胃肠道血管炎。鉴于胃肠道组织学上没有血管特征,本例皮肤LCV与结肠炎之间的关系仍然是相关的,而不是证实的。本病例强调了在怀疑LCV有皮外表现时谨慎诊断的重要性。
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
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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