Marian Rosel D Villaverde, Juan Paolo David S Villena, Claudine Yap Silva
{"title":"一种奇特的模式:伴有肉芽肿性皮炎的结节性继发性梅毒","authors":"Marian Rosel D Villaverde, Juan Paolo David S Villena, Claudine Yap Silva","doi":"10.47895/amp.v58i17.9040","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":6994,"journal":{"name":"Acta Medica Philippina","volume":"58 17","pages":"60-63"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11484585/pdf/","citationCount":"0","resultStr":"{\"title\":\"A Peculiar Pattern: Nodular Secondary Syphilis with Granulomatous Dermatitis.\",\"authors\":\"Marian Rosel D Villaverde, Juan Paolo David S Villena, Claudine Yap Silva\",\"doi\":\"10.47895/amp.v58i17.9040\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":6994,\"journal\":{\"name\":\"Acta Medica Philippina\",\"volume\":\"58 17\",\"pages\":\"60-63\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11484585/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Medica Philippina\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.47895/amp.v58i17.9040\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Medica Philippina","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47895/amp.v58i17.9040","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
摘要
结节型梅毒伴有肉芽肿性炎症组织病理学模式,是继发性梅毒中一种不常见的皮肤表现,可能会给临床医生和病理学家的诊断带来挑战。一名33岁的男性患者被诊断为艾滋病病毒感染者,5周前出现无症状的全身红斑丘疹和结节,上覆鳞屑,手掌和足底受累。对前臂的一个结节进行组织病理学检查后发现,在由淋巴细胞、上皮样和泡沫组织细胞、浆细胞、中性粒细胞和多核巨细胞组成的混合细胞炎症浸润背景下,出现了非酪氨酸肉芽肿。Warthin-Starry染色法显示有螺旋体,而Fite-Faraco和Periodic Acid-Schiff染色法则分别显示无耐酸杆菌和真菌。快速血浆反应蛋白(RPR)呈反应性(1:256)。患者接受了单剂量苄星青霉素 G 240 万单位肌肉注射,皮损完全消退,RPR 滴度下降了 8 倍。结节性病变是继发性梅毒不常见的皮肤表现,相关的组织病理学发现肉芽肿炎症模式也不常见,这给诊断带来了挑战。随着梅毒发病率的不断上升,尤其是在艾滋病患者中,皮肤科医生、皮肤病理学家、内科医生和传染病专家应注意梅毒的此类表现。
A Peculiar Pattern: Nodular Secondary Syphilis with Granulomatous Dermatitis.
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.