Mondal Dinesh, Hamano Shinjiro, Hasnain Golam, Satoskar Abhay R
Centre for Nutrition and Food Security, Parasitology Laboratory, (icddr, b) Mohakhali, Dhaka, Bangladesh.
Department of Parasitology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan.
Res Rep Trop Med. 2014 Nov 14;5:105-111. doi: 10.2147/RRTM.S35707. eCollection 2014.
Post kala-azar dermal leishmaniasis (PKDL) is a skin complication resulting from infection with (LD) parasite. It mostly affects individuals who have previously suffered from visceral leishmaniasis (VL) caused by LD. In some cases, PKDL develops among people infected with LD, but do not show any symptoms of VL. Clinical presentation includes hypopigmented macules/papules/nodules or polymorphic lesions (combination of two or more lesions). Except for skin lesions, PKDL patients are generally healthy and usually do not seek medical care. These patients play an important role in interepidemic transmission of the infection and subsequent VL outbreak. Therefore, proper diagnosis and treatment of PKDL patients is important for the control of VL in endemic countries, especially in the Indian subcontinent where VL is anthroponotic. Here, we report the challenges in the estimation of PKDL burden, its diagnosis, and treatment, and suggest possible solutions based on recent literature, reports, published manuals, and web-based information.
黑热病后皮肤利什曼病(PKDL)是由杜氏利什曼原虫(LD)感染引起的一种皮肤并发症。它主要影响既往曾患由LD所致内脏利什曼病(VL)的个体。在某些情况下,PKDL在感染LD但未表现出任何VL症状的人群中发生。临床表现包括色素减退性斑疹/丘疹/结节或多形性皮损(两种或更多皮损的组合)。除皮肤损害外,PKDL患者一般健康,通常不会寻求医疗护理。这些患者在感染的流行间期传播及随后的VL暴发中起重要作用。因此,对PKDL患者进行正确诊断和治疗对于流行国家控制VL很重要,尤其是在VL为人源性的印度次大陆地区。在此,我们报告了PKDL负担评估、诊断及治疗方面的挑战,并根据近期文献、报告、已发布手册及网络信息提出了可能的解决方案。