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肉芽肿性滤泡性二期梅毒:一个不寻常的组织病理学线索。

Granulomatous Folliculotropic Secondary Syphilis: An Unusual Histopathological Clue.

机构信息

Dermatopathology Duisburg-Essen, Essen, Germany.

出版信息

Am J Dermatopathol. 2024 Dec 1;46(12):839-841. doi: 10.1097/DAD.0000000000002821. Epub 2024 Aug 14.

Abstract

Syphilis is a sexually transmitted disease that can present a wide variety of clinical and histopathological manifestations. We present the case of a 75-year-old patient with a persistent maculopapular rash on the trunk and extremities, in which the biopsy showed an exclusively perifollicular granulomatous infiltrate. In the immunohistochemical staining with anti- Treponema pallidum antibodies, spirochetes scattered within the perifollicular inflammatory infiltrate were identified. These findings together with the serological analysis allowed the diagnosis of secondary syphilis. Folliculotropic nonalopecic syphilis is rare, and the pathogenic mechanisms that cause this specific tropism are unknown. On the other hand, granulomatous inflammation is a pattern typically described in tertiary syphilis but also occasionally found in secondary syphilis. We present a case of secondary syphilis with the combination of both histopathological findings, an uncommon constellation for dermatopathologists to consider.

摘要

梅毒是一种性传播疾病,可呈现出多种多样的临床和组织病理学表现。我们报告了 1 例 75 岁患者,其躯干和四肢出现持续的斑丘疹,活检显示仅为毛囊周围肉芽肿性浸润。在抗梅毒螺旋体抗体的免疫组化染色中,发现螺旋体散在分布于毛囊周围炎症浸润中。这些发现以及血清学分析有助于诊断二期梅毒。毛囊性非瘢痕性梅毒较为罕见,导致这种特定亲嗜性的发病机制尚不清楚。另一方面,肉芽肿性炎症是三期梅毒的典型表现模式,但偶尔也可见于二期梅毒。我们报告了 1 例二期梅毒合并这两种组织病理学发现的病例,这对皮肤科病理学家来说是一种不常见的组合,需要考虑。

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