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一种奇特的模式:伴有肉芽肿性皮炎的结节性二期梅毒。

A Peculiar Pattern: Nodular Secondary Syphilis with Granulomatous Dermatitis.

作者信息

Villaverde Marian Rosel D, Villena Juan Paolo David S, Yap Silva Claudine

机构信息

Department of Dermatology, Philippine General Hospital, University of the Philippines Manila.

出版信息

Acta Med Philipp. 2024 Sep 30;58(17):60-63. doi: 10.47895/amp.v58i17.9040. eCollection 2024.

Abstract

Nodular syphilis with a granulomatous inflammatory histopathologic pattern is an uncommon cutaneous presentation of secondary syphilis which could pose a diagnostic challenge for clinicians and pathologists alike. A 33-year-old male diagnosed with HIV presented with a 5-week history of asymptomatic generalized erythematous papules and nodules with overlying scales, with involvement of the palms and soles. Histopathologic examination of a nodule from the forearm revealed non-caseating granulomas in a background of a mixed cell inflammatory infiltrate composed of lymphocytes, epithelioid and foamy histiocytes, plasma cells, neutrophils, and multinucleated giant cells. Warthin-Starry Stain revealed spirochetal organisms, while Fite-Faraco and Periodic Acid-Schiff stains were negative for acid-fast bacilli and fungal elements, respectively. Rapid plasma reagin (RPR) was reactive (1:256). Patient was given a single dose of benzathine penicillin G 2.4 million units intramuscularly, with noted complete resolution of skin lesions as well as an 8-fold decrease in RPR titers. Nodular lesions are an uncommon cutaneous manifestation of secondary syphilis, and the associated histopathologic finding of granulomatous inflammatory pattern is also unusual, posing a diagnostic challenge. With the increasing prevalence of syphilis, especially among HIV patients, dermatologists, dermatopathologists, internists, and infectious disease specialists should be aware of such presentations of syphilis.

摘要

具有肉芽肿性炎症组织病理学模式的结节性梅毒是二期梅毒一种不常见的皮肤表现形式,这可能给临床医生和病理学家带来诊断挑战。一名33岁诊断为HIV的男性患者,出现了5周无症状的全身性红斑丘疹和结节,伴有鳞屑,累及手掌和足底。对取自前臂的一个结节进行组织病理学检查显示,在由淋巴细胞、上皮样和泡沫状组织细胞、浆细胞、中性粒细胞和多核巨细胞组成的混合细胞炎性浸润背景中存在非干酪样肉芽肿。Warthin-Starry染色显示螺旋体微生物,而Fite-Faraco染色和过碘酸希夫染色分别对抗酸杆菌和真菌成分呈阴性。快速血浆反应素(RPR)呈阳性(1:256)。患者接受了一剂240万单位苄星青霉素G肌肉注射,皮肤病变完全消退,RPR滴度下降了8倍。结节性病变是二期梅毒一种不常见的皮肤表现,与之相关的肉芽肿性炎症模式的组织病理学发现也不寻常,这带来了诊断挑战。随着梅毒患病率的上升,尤其是在HIV患者中,皮肤科医生、皮肤病理学家、内科医生和传染病专家应了解梅毒的此类表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2a/11484585/037753e3c702/AMP-58-17-9040-g001.jpg

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