Bhargava Aradhana, Ramesh V, Verma Sandeep, Salotra Poonam, Bala Manju
Apex Regional STD Teaching, Training and Research Centre, Safdarjung Hospital, Department of STD and Dermatology, Safdarjung Hospital, New Delhi, India.
Parasitology Laboratory, National Institute of Pathology (Indian Council of Medical Research), New Delhi, India.
Indian J Dermatol Venereol Leprol. 2018 Nov-Dec;84(6):690-695. doi: 10.4103/ijdvl.IJDVL_970_16.
Post kala azar dermal leishmaniasis (PKDL) is a neglected dermatosis that develops as a sequel to kala azar after apparent complete treatment. Being a non life threatening condition, patients often delay treatment thereby maintaining a reservoir of infection. The diagnosis of PKDL rests on the demonstration of the parasite in tissue smears, immune diagnosis by detection of parasite antigen or antibody in blood, or detection and quantitation of parasite DNA in tissue specimens. Sophisticated molecular tests are not only expensive but also need skilled hands and expensive equipment. To be useful, diagnostic methods must be accurate, simple and affordable for the population for which they are intended.
This study was designed to assess functionality and operational feasibility of slit-skin smear examination.
Sensitivity and specificity was evaluated by performing slit-skin smear and histo-pathological examination in 46 PKDL patients and the results were compared with the parasite load in both the slit aspirate and tissue biopsy specimens by performing quantitative Real-time PCR (Q-PCR).
The slit-skin smear examination was more sensitive than tissue biopsy microscopy. The parasite loads significantly differed among various types of clinical lesions (P < 0.05). The threshold of parasite load for detection by SSS microscopy was 4 parasites/μl in slit aspirate and 60 parasites/μg tissue DNA in tissue biopsy while that for tissue microscopy was 63 parasites/μl and 502 parasites/μg tissue DNA respectively. As detection of Leishmania donovani bodies may be challenging in inexperienced hands, the microscopic structure of these has been detailed along with a comprehensive discussion of pre analytical, analytical and post analytical variables affecting its identification. To facilitate the diagnosis of PKDL, some scenarios have been suggested taking into consideration the clinical, epidemiological, immunological and microscopic aspects.
Such evidence based medicine helps minimize intuition, systematize clinical experience and provides a diagnostic rationale as sufficient grounds for a clinical decision.
黑热病后皮肤利什曼病(PKDL)是一种被忽视的皮肤病,在黑热病明显完全治愈后作为后遗症出现。由于它并非危及生命的疾病,患者常常延迟治疗,从而维持了一个感染源。PKDL的诊断依赖于在组织涂片中发现寄生虫、通过检测血液中的寄生虫抗原或抗体进行免疫诊断,或检测和定量组织标本中的寄生虫DNA。复杂的分子检测不仅昂贵,而且需要技术熟练的人员和昂贵的设备。要有用,诊断方法必须准确、简单且对其适用人群来说负担得起。
本研究旨在评估皮肤刮片检查的功能和操作可行性。
对46例PKDL患者进行皮肤刮片和组织病理学检查,评估其敏感性和特异性,并通过定量实时PCR(Q-PCR)将结果与皮肤刮取物和组织活检标本中的寄生虫载量进行比较。
皮肤刮片检查比组织活检显微镜检查更敏感。不同类型的临床病变之间寄生虫载量有显著差异(P < 0.05)。皮肤刮片显微镜检查检测的寄生虫载量阈值在皮肤刮取物中为4个寄生虫/微升,在组织活检中为60个寄生虫/微克组织DNA,而组织显微镜检查的阈值分别为63个寄生虫/微升和502个寄生虫/微克组织DNA。由于在经验不足的人员手中检测杜氏利什曼原虫体可能具有挑战性,因此详细描述了其微观结构,并全面讨论了影响其识别的分析前、分析中和分析后变量。为便于PKDL的诊断,考虑到临床、流行病学、免疫学和显微镜检查方面,提出了一些情况。
这种循证医学有助于减少直觉、使临床经验系统化,并为临床决策提供充分依据的诊断原理。