Suppr超能文献

慢性无鞭毛体阴性皮肤利什曼病:27例临床、组织病理学及分子学研究,重点关注非典型和假淋巴瘤表现

Chronic amastigote-negative cutaneous leishmaniasis: A clinical, histopathologic and molecular study of 27 cases with emphasis on atypical and pseudolymphomatous presentations.

作者信息

Tomasini Carlo, Moneghini Laura, Barbui Anna M

机构信息

Dermatopathology Unit, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza, Turin, Italy.

Division of Pathology, Department of Health Sciences, University of Milan, Hospital San Paolo, Milan, Italy.

出版信息

J Cutan Pathol. 2017 Jun;44(6):530-537. doi: 10.1111/cup.12927. Epub 2017 Apr 10.

Abstract

BACKGROUND

Chronic amastigote-negative cutaneous leishmaniasis (CL) is a diagnostic challenge, as the parasite load may be low, or absent in biopsy tissue sections.

METHODS

A series of consecutive biopsy specimens, taken from 130 patients with a diagnosis of granulomatous dermatitis of unknown etiology, were reviewed. Polymerase chain reaction (PCR) was carried out for Leishmania-specific DNA.

RESULTS

A total of 27 of 130 samples were positive for Leishmania-specific DNA. In only 3 patients was a clinical diagnosis CL made. The lesions were, single or multiple nodules or plaques of many months duration. Histopathologically, a tuberculoid granulomatous dermatitis was the least common denominator in every case, whilst in 5 cases a heavy lymphoid component was predominant. One patient had a concurrent cutaneous marginal zone lymphoma (MZL), the additional PCR study showed the presence of Leishmania DNA in tissue.

CONCLUSIONS

The results of this study expand on previous observations as to the deceptive clinicopathologic manifestations of chronic CL, confirming the diagnostic value of PCR analysis for Leishmania DNA in unspecified granulomatous dermatitides. We also suggest that, in countries where Leishmaniasis is endemic, PCR for Leishmania-specific DNA be performed in any idiopathic pseudolymphomatous. More compelling evidence as to whether chronic Leishmania infection is implicated in the pathogenesis of some cutaneous MZL is warranted by further studies.

摘要

背景

慢性无鞭毛体阴性皮肤利什曼病(CL)是一项诊断挑战,因为活检组织切片中的寄生虫负荷可能很低或不存在。

方法

回顾了一系列连续的活检标本,这些标本取自130例被诊断为病因不明的肉芽肿性皮炎的患者。对利什曼原虫特异性DNA进行聚合酶链反应(PCR)。

结果

130份样本中共有27份利什曼原虫特异性DNA呈阳性。仅3例患者临床诊断为CL。病变为持续数月的单个或多个结节或斑块。组织病理学上,结核样肉芽肿性皮炎是每个病例中最常见的特征,而在5例中,大量淋巴细胞成分占主导。1例患者同时患有皮肤边缘区淋巴瘤(MZL),进一步的PCR研究显示组织中存在利什曼原虫DNA。

结论

本研究结果扩展了以往关于慢性CL具有欺骗性临床病理表现的观察结果,证实了PCR分析在未明确的肉芽肿性皮炎中对利什曼原虫DNA的诊断价值。我们还建议,在利什曼病流行的国家,对任何特发性假性淋巴瘤都应进行利什曼原虫特异性DNA的PCR检测。关于慢性利什曼原虫感染是否与某些皮肤MZL的发病机制有关,需要进一步研究提供更有说服力的证据。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验