Arora Shikha, D'Souza Paschal, Haroon Mohammad A, Ramesh V, Kaur Onkar, Chandoke Raj Kumar
Department of Dermatology and Venereology, ESIC (Employees' State Insurance Corp.) Postgraduate Institute of Medical Sciences and Research (PGIMSR), New Delhi, India.
Int J Dermatol. 2014 May;53(5):606-8. doi: 10.1111/ijd.12299. Epub 2013 Dec 10.
Post-kala-azar dermal leishmaniasis (PKDL) is well recognized in the Indian subcontinent and is not infrequently confused with leprosy. The present report describes findings in an unusual case of PKDL.
We report an adult male who presented with firm nodules on the face and extremities, along with hypopigmented macules on the neck with deformity and hypoesthesia over the right upper extremity. The patient had experienced similar lesions seven years previously and had used multibacillary multi-drug therapy for leprosy with complete resolution of the nodules.
At the current presentation, skin smears from ear lobes and nodules were negative on Ziehl-Neelsen staining. Histopathological examination revealed a dermal lymphohistiocytic infiltrate with plasma cells. Giemsa staining of a tissue smear revealed Leishmania donovani bodies, and an rK39 antigen test was positive. The patient responded well to oral miltefosine.
This case is noteworthy because the patient exhibited an unusual combination of healed leprosy sequelae and active PKDL lesions, which caused a diagnostic dilemma.
黑热病后皮肤利什曼病(PKDL)在印度次大陆已得到充分认识,且常与麻风病混淆。本报告描述了一例不寻常的PKDL病例的发现。
我们报告一名成年男性,其面部和四肢出现坚实结节,颈部有色素减退斑,右上肢有畸形和感觉减退。该患者七年前曾出现过类似病变,并接受了多菌型麻风病联合化疗,结节完全消退。
在本次就诊时,耳垂和结节的皮肤涂片经齐-尼氏染色呈阴性。组织病理学检查显示真皮淋巴细胞和组织细胞浸润,并伴有浆细胞。组织涂片吉姆萨染色显示杜氏利什曼原虫体,rK39抗原检测呈阳性。该患者对口服米替福新反应良好。
该病例值得注意,因为患者表现出愈合的麻风病后遗症与活动性PKDL病变的不寻常组合,这导致了诊断困境。