Salam Md A, Siddiqui Muhammad A, Nabi Shah G, Bhaskar Khondaker R H, Mondal Dinesh
Department of Microbiology, Rajshahi Medical College, Rajshahi 6000, Bangladesh.
J Health Popul Nutr. 2013 Jun;31(2):294-7. doi: 10.3329/jhpn.v31i2.16395.
Post-kala-azar dermal leishmaniasis (PKDL) is a dermatologic manifestation that usually occurs after visceral leishmaniasis (VL) caused by Leishmania donovani. It is characterized by hypopigmented patches, a macular or maculopapular rash and nodular skin lesions on the body surface. Involvement of the mucosae is very rare and unusual in PKDL. We report a case of PKDL that presented with polymorphic skin lesions, along with involvement of peri-oral mucosa and tongue from an endemic area for kala-azar in Bangladesh. In the absence of a definite past history of kala-azar, a clinical suspicion for PKDL was confirmed by positive rapid serological tests against two recombinant (rK39 and rK28) leishmanial antigens, demonstration of Leishmania donovani (LD) body in the slit skin smear, and isolation of promastigotes by culture from a nodular lesion. The patient was treated with oral Miltefosine for three consecutive months and showed significant clinical improvement as demonstrated by a negative slit skin smear at two months after initiation of therapy. We report this case as an unusual presentation of mucosal involvement in PKDL and subsequent treatment success with Miltefosine.
黑热病后皮肤利什曼病(PKDL)是一种皮肤病表现,通常发生在由杜氏利什曼原虫引起的内脏利什曼病(VL)之后。其特征为体表出现色素减退斑、斑疹或斑丘疹皮疹以及结节性皮肤病变。在PKDL中,黏膜受累非常罕见且不常见。我们报告一例来自孟加拉国黑热病流行地区的PKDL病例,该病例呈现多形性皮肤病变,同时伴有口周黏膜和舌部受累。在缺乏明确的黑热病既往史的情况下,针对两种重组(rK39和rK28)利什曼原虫抗原的快速血清学检测呈阳性、在皮肤涂片检查中发现杜氏利什曼原虫(LD) bodies以及从结节性病变培养物中分离出前鞭毛体,证实了对PKDL的临床怀疑。该患者连续三个月接受口服米替福新治疗,治疗开始两个月后皮肤涂片检查呈阴性,显示出显著的临床改善。我们将此病例报告为PKDL黏膜受累的不寻常表现以及随后使用米替福新治疗成功的案例。