Department of Dermatology, Bhaskar Medical College, Hyderabad, India.
Indian J Dermatol Venereol Leprol. 2016 May-Jun;82(3):252-61. doi: 10.4103/0378-6323.179086.
Pure neuritic leprosy has always been an enigma due to its clinical and management ambiguities. Although only the Indian Association of Leprologist's classification recognizes 'pure neuritic leprosy' as a distinct sub group of leprosy, cases nonetheless are reported from various countries of Asia, Africa, South America and Europe, indicating its global relevance. It is important to maintain pure neuritic leprosy as a subgroup as it constitutes a good percentage of leprosy cases reported from India, which contributes to more than half of global leprosy numbers. Unfortunately, a high proportion of these patients present with Grade 2 disability at the time of initial reporting itself due to the early nerve involvement. Although skin lesions are absent by definition, when skin biopsies were performed from the skin along the distribution of the affected nerve, a proportion of patients demonstrated leprosy pathology, revealing sub-clinical skin involvement. In addition on follow-up, skin lesions are noted to develop in up to 20% of pure neuritic leprosy cases, indicating its progression to manifest cutaneous disease. Over the decades, the confirmation of diagnosis of pure neuritic leprosy has been subjective, however, with the arrival and use of high-resolution ultrasonography (HRUS) for nerve imaging, we have a tool not only to objectively measure and record the nerve thickening but also to assess the morphological alterations in the nerve including echo texture, fascicular pattern and vascularity. Management of pure neuritic leprosy requires multidrug therapy along with appropriate dose of systemic corticosteroids, for both acute and silent neuritis. Measures for pain relief, self-care of limbs and physiotherapy are important to prevent as well as manage disabilities in this group of patients.
单纯神经炎型麻风一直是一个谜,因为它的临床表现和处理都存在不确定性。尽管只有印度麻风协会的分类将“单纯神经炎型麻风”作为麻风的一个独特亚组来识别,但来自亚洲、非洲、南美洲和欧洲的各个国家仍有病例报告,表明其具有全球相关性。将单纯神经炎型麻风作为一个亚组保留下来很重要,因为它构成了印度报告的麻风病例中的很大一部分,占全球麻风病例的一半以上。不幸的是,由于早期神经受累,这些患者中有很大一部分在初次报告时就已经存在 2 级残疾。尽管根据定义皮肤损害不存在,但当沿受累神经分布的皮肤进行皮肤活检时,一部分患者显示出麻风病理学,表明存在亚临床皮肤受累。此外,在随访中,多达 20%的单纯神经炎型麻风患者会出现皮肤损害,表明其进展为显性皮肤疾病。几十年来,单纯神经炎型麻风的诊断确认一直是主观的,然而,随着高分辨率超声(HRUS)用于神经成像的到来和使用,我们不仅有了一种客观测量和记录神经增厚的工具,还可以评估神经的形态改变,包括回声纹理、束状模式和血管。单纯神经炎型麻风的治疗需要多药治疗,同时还需要适当剂量的全身皮质类固醇,用于治疗急性和无症状神经炎。对于这组患者,缓解疼痛、肢体自我护理和物理治疗等措施对于预防和管理残疾非常重要。