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生殖器部位水疱样假性疣状丘疹和结节,见于 4 岁大小便失禁患者。

A vesicular variant of pseudoverrucous papules and nodules in the genital area of an incontinent 4-year-old.

机构信息

Northern Clinical School, University of Sydney, Royal North Shore Hospital, St Leonards, Australia.

出版信息

Australas J Dermatol. 2013 Nov;54(4):e92-4. doi: 10.1111/j.1440-0960.2012.00952.x. Epub 2012 Oct 9.

Abstract

Irritant contact dermatitis is a common cause of chronic vulvitis in patients wearing diapers and incontinence garments. In most cases the diagnosis is obvious; however, atypical presentations may mimic more serious dermatoses. We present a 4-year-old girl who presented at birth with cloacal atresia corrected surgically and resulting in chronic incontinence requiring full-time diapers. She presented with crops of herpetiform vesicles and bullae on a base that ranged from normal skin to severe erythema and oedema. A histological examination revealed a well-demarcated lesion showing a thickened epidermis with hyperkeratosis and parakeratosis, acanthosis and an abrupt transition to pallor of the upper half. Focal full thickness epidermis necrosis and small areas of spongiosis, acantholysis and apoptotic keratinocytes were seen. Immunofluorescence was negative. The lesions improved with the treatment of secondary infection and minimal topical therapy with an emollient only. This case represents an unusual vesicular variant of pseudoverrucous papules and nodules, which has been reported only once previously.

摘要

刺激性接触性皮炎是穿着尿布和失禁服的患者慢性外阴炎的常见原因。大多数情况下,诊断是明显的;然而,不典型的表现可能类似于更严重的皮肤病。我们介绍了一个 4 岁的女孩,她出生时患有直肠阴道隔闭锁,经手术矫正,导致慢性失禁,需要全天使用尿布。她表现为疱疹样水疱和大疱,基底从正常皮肤到严重红斑和水肿不等。组织学检查显示边界清楚的病变,表皮增厚,伴有角化过度和角化不全、棘皮症和上半部分突然变白。可见全层表皮坏死和小面积海绵形成、棘层松解和凋亡角质形成细胞。免疫荧光为阴性。在治疗继发感染和仅使用保湿剂进行最小量局部治疗后,病变得到改善。该病例代表了一种罕见的水疱性假疣状丘疹和结节变异型,以前仅报告过一例。

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