Localized Bullous Pemphigoid in a Patient with Acquired Reactive Perforating Collagenosis.

IF 0.9 Q4 DERMATOLOGY Case Reports in Dermatology Pub Date : 2023-01-01 DOI:10.1159/000528140
Masahiro Oka
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引用次数: 1

Abstract

A 61-year-old man presented with 6-month and 5-day histories of multiple, pruritic nodular eruptions on the trunk and extremities and bullous eruptions on the left foot, respectively. The nodular eruptions had been treated with topical corticosteroids without improvement. He had been diagnosed with diabetes mellitus at the age of 42 years and had been suffering from end-stage renal disease for 1 year. Physical examination revealed scattered violet-brown papules and nodules on the trunk and extremities, many of which had central umbilicated necrosis or keratin plugs. Additionally, two tense bullae and five erosions were noted on the dorsal aspect of the left foot. Laboratory tests showed elevated levels of serum anti-bullous pemphigoid (BP)180 antibody. Histopathological findings of a nodule and a bulla were compatible with those of acquired reactive perforating collagenosis (ARPC) and BP, respectively. The papular and nodular lesions were diagnosed as ARPC, while bullous and erosive lesions were diagnosed as localized BP. The present case, together with previously reported cases of coexisting generalized BP and ARPC, suggests that coexistence of BP, regardless of whether generalized or localized, is significantly associated with ARPC.

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获得性反应性穿孔性胶原沉积患者的局限性大疱性类天疱疮。
61岁男性,6个月和5天,躯干和四肢多发瘙痒性结节性皮疹,左脚大疱性皮疹。结节性爆发曾用局部皮质类固醇治疗,但未见改善。他在42岁时被诊断出患有糖尿病,并患有终末期肾脏疾病1年。体格检查发现躯干和四肢散在紫棕色丘疹和结节,其中许多有中央脐状坏死或角蛋白塞。此外,在左脚背侧发现2个紧绷大泡和5个糜烂。实验室检查显示血清抗大疱性类天疱疮(BP)180抗体水平升高。结节和大疱的组织病理学结果分别与获得性反应性穿孔性胶原症(ARPC)和BP的组织病理学结果一致。丘疹和结节性病变诊断为ARPC,大疱性和糜烂性病变诊断为局限性BP。本病例,连同先前报道的广泛性BP和ARPC共存的病例,表明BP的共存,无论是广泛性BP还是局部性BP,都与ARPC显著相关。
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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
57
审稿时长
9 weeks
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