1Departments of Dermatology Unit-II, Christian Medical College, Vellore, India.
2Infectious Diseases, Christian Medical College, Vellore, India.
Am J Trop Med Hyg. 2020 Dec 29;104(3):928-933. doi: 10.4269/ajtmh.20-0938.
Leishmaniasis is endemic in the Indian subcontinent with predominance of visceral leishmaniasis (VL) due to Leishmania donovani. Cutaneous leishmaniasis (CL) is uncommon, and mucocutaneous leishmaniasis (MCL) is rarely reported in this region. Recent reports reveal a changing epidemiology and atypical manifestations. A retrospective study of 52 suspected cases with cutaneous and mucosal involvement seen from January 2008 to December 2018 in a tertiary care setting in a non-endemic state in southern India is reported. Twelve patients were confirmed to have leishmaniasis; seven had MCL, two had CL, and three had post-kala-azar dermal leishmaniasis (PKDL). All cases were male, with a median age of 41.5 years (interquartile range, 30-55.5 years), and the median duration of the disease was 6 years (interquartile range, 1-9.5 years). Patients with MCL had mucosal involvement including destructive ulcero-proliferative lesions due to delayed diagnosis; none had a history of travel to countries endemic for MCL and all were attributable to L. donovani species. On the other hand, Leishmania major which was the causative species in both CL patients was associated with travel to the Middle East. Patients with PKDL presented with multiple plaques and hypopigmented patches; one had concomitant VL and all were from endemic areas. Hitherto uncommon MCL, caused by potentially atypical variants of L. donovani, has emerged as a new manifestation of leishmaniasis in this region. A high index of suspicion based on lesions seen and history of travel combined with PCR-based diagnostics are required to confirm diagnosis for the various skin manifestations of leishmaniasis.
利什曼病在印度次大陆流行,由于感染杜氏利什曼原虫,以内脏利什曼病(VL)为主。皮肤利什曼病(CL)较为少见,粘膜利什曼病(MCL)在该地区罕见报道。最近的报告显示,该疾病的流行病学和临床表现正在发生变化。本文报告了在印度南部一个非流行地区的三级保健机构中,2008 年 1 月至 2018 年 12 月间对 52 例皮肤和粘膜受累疑似病例进行的回顾性研究。12 例患者被确诊患有利什曼病;7 例为 MCL,2 例为 CL,3 例为黑热病后皮肤利什曼病(PKDL)。所有病例均为男性,中位年龄为 41.5 岁(四分位间距,30-55.5 岁),中位疾病持续时间为 6 年(四分位间距,1-9.5 年)。MCL 患者存在粘膜受累,包括因诊断延迟而出现破坏性溃疡增殖性病变;所有患者均无前往 MCL 流行国家的旅行史,均归因于杜氏利什曼原虫种。另一方面,在 CL 患者中引起疾病的利什曼原虫属主要种与前往中东有关。PKDL 患者表现为多个斑块和色素减退斑;1 例同时患有 VL,所有患者均来自流行地区。迄今为止,在该地区,由潜在非典型杜氏利什曼原虫变种引起的不常见的 MCL 已成为利什曼病的一种新表现。基于所见病变和旅行史,以及聚合酶链反应(PCR)为基础的诊断,提高对利什曼病各种皮肤表现的怀疑指数,是确诊所必需的。