A clinico-pathological study of primary neuritic leprosy.

Leprosy in India Pub Date : 1983-04-01
V K Pannikar, S Arunthathi, C J Chacko, E P Fritschi
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Abstract

Normally neural involvement in leprosy is an ascending neuritis from the nerve involvement in the dermal lesions. However, in some cases neural involvement is seen in the absence of any dermal lesions. In some of these pure neuritic cases, dermal lesions appear sometime later. It is, therefore, more appropriate to designate such cases as 'primary neuritic' cases. This study is aimed at diagnosing primary neuritic leprosy among patients presenting with only neuritic symptoms. An attempt is also made to classify primary neuritic leprosy on a clinical and histopathological basis. During the period 1979-80, 30 patients reported to the out patient department of Schieffelin Leprosy Research and Training Centre, Karigiri with complaints of neuritic origin. In addition to clinical examination and routine skin smears, investigations such as skin, nerve and nasal biopsies, nerve conduction velocity and lepromin testing were carried out where feasible. 17 of these patients were diagnosed as primary neuritic leprosy and in 7 patients other neurological conditions were diagnosed. The remaining 6 patients were kept under observation and have not shown evidence of leprosy during a two year period of following-up. It is interesting that 4 of the 17 primary neuritic cases developed patches during follow-up period of two years. In the final analysis 7 patients (41.2%) were classified into the lepromatous group and 10 patients (58.8%) in the non-lepromatous group (Table-6). This classification will have a bearing on duration of treatment and for their subsequent release from control.

原发性神经性麻风病的临床病理研究。
通常情况下,麻风病的神经受累是由皮肤病变的神经受累引起的上行神经炎。然而,在一些病例中,在没有任何皮肤病变的情况下可以看到神经受累。在这些纯粹的神经炎病例中,皮肤病变会在稍后出现。因此,将此类病例称为“原发性神经炎”病例更为合适。本研究的目的是诊断原发性神经性麻风病患者中只有神经性症状。还尝试在临床和组织病理学基础上对原发性神经性麻风进行分类。1979- 1980年期间,Karigiri的希effelin麻风病研究和培训中心的门诊部报告了30名患者,他们的主诉是神经性疾病。除了临床检查和常规皮肤涂片外,在可行的情况下还进行了皮肤、神经和鼻腔活检、神经传导速度和麻黄素检测等调查。其中17名患者被诊断为原发性神经性麻风病,7名患者被诊断为其他神经系统疾病。其余6名患者仍在观察中,在两年随访期间未显示麻风病的证据。有趣的是,17例原发性神经炎病例中有4例在随访2年期间出现了斑块。最终,7例患者(41.2%)被归为麻风组,10例患者(58.8%)被归为非麻风组(表6)。这种分类将影响到治疗的持续时间和随后的控制释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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