[Histoid leprosy in Morocco: retrospective study of 18 cases].

F Hali, H Benchikhi, A Latifi, J Boukry, F Smahi, M Sbai
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Abstract

Introduction: Histoid leprosy is a special and rare anatomoclinical form of multibacillary leprosy. Most of the few large series describing this entity In literature have been reported from India. The purpose of this study was to analyze the epidemiological, clinical and therapeutic characteristics of patients with histoid leprosy in Morocco.

Material and methods: This retrospective study was conducted at the National Centre of Leprology (CNL) in Casablanca from January 1991 to December 2006. Only histologially confirmed cases of histoid leprosy were included. Epidemiological, clinical, histological and therapeutic characteristics were compiled from records and analyzed using EPI-Info version 6.

Results: Confirmed histoid leprosy accounted for 18 of the new cases of leprosy recorded at CNL recorded during the 16-year study period. There were 13 men and 5 women with a mean age of 35.2 years. Family exposure was noted in 9 patients (50%) including two who had more than two relatives with leprosy. Nodules/subcutaneous nodules were the most common morphological pattern (88.8%). Neurological involvement was found in 10 patients. Seven patients had grade 1 deformities. Slit skin smears from histoid lesions revealed abundant bacilli with a high bacteriological index ranging from 3 + to 5 + according to the Ridley index. All patients received antibiotic treatment according to the Moroccan protocol. Outcome was favorable in all patients. Six patients (33.3%) developed erythema nodosum leprosum during the course of disease. With a average follow-up of 9 years, no recurrence has been observed.

Discussion: Because of its multibacillary character and despite its rarity, histoid leprosy poses a challenge to the leprosy eradication in Morocco. Like other forms of multibacillary leprosy, histoid leprosy requires early detection and prompt multidrug therapy. These requirments should be made a priority in the national program against leprosy.

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[摩洛哥组织麻风病:18例回顾性研究]。
组织样麻风是一种特殊的、罕见的多菌性麻风解剖临床形式。文献中描述这一实体的为数不多的大型系列大多来自印度。本研究的目的是分析摩洛哥麻风病的流行病学、临床和治疗特点。材料和方法:本回顾性研究于1991年1月至2006年12月在卡萨布兰卡国家麻风中心(CNL)进行。仅包括组织学证实的麻风病病例。从记录中收集流行病学、临床、组织学和治疗特征,并使用EPI-Info version 6进行分析。结果:在16年的研究期间,CNL记录的麻风新病例中有18例确诊为组织性麻风。男性13人,女性5人,平均年龄35.2岁。9名患者(50%)有家庭接触史,包括两名有两名以上亲属患有麻风病的患者。结节/皮下结节是最常见的形态(88.8%)。10例患者发现神经系统受累。7例患者为1级畸形。组织病变的切口皮肤涂片显示大量杆菌,细菌学指数高,根据Ridley指数在3 +至5 +之间。所有患者均按照摩洛哥方案接受抗生素治疗。所有患者的预后均良好。6例(33.3%)患者在病程中出现麻风结节性红斑。平均随访9年,未见复发。讨论:由于其多菌性和罕见性,麻风病对摩洛哥的麻风病根除工作提出了挑战。与其他形式的多菌性麻风病一样,组织性麻风病需要早期发现并及时进行多种药物治疗。这些要求应作为防治麻风病国家规划的优先事项。
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