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Wade histoid leprosy revisited

机译:韦德组蛋白麻风病再次发作

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An 18-year-old man presented with a 4-year history of erythematous patches on the trunk, followed 2-years later by multiple nodules, mostly located on the limbs, and distal paresthesias. Two close contacts were treated for leprosy during his childhood. Histopathological examination revealed a histiocytic infiltrate with acid-fast bacilli on Ziehl-Neelsen stain. The slit-skin and nasal smears showed numerous acid-fast bacilli. The correlation between clinical, epidemiological, histopathological, and microbiological features allowed the diagnosis of lepromatous leprosy, histoid variant. Multidrug therapy as recommended by the WHO was initiated. A rapid and sustained improvement was seen. Histoid leprosy is a rare manifestation of lepromatous leprosy, first described by Wade in 1960. Since then few cases have been reported, the majority of them from countries with a high prevalence of the disease. Early recognition and treatment are of most importance to prevent neurological disabilities and achieve epidemiological control.
机译:一名18岁男子在躯干上出现了4年的红斑斑病史,两年后又出现了多个结节,大部分位于四肢和远端感觉异常。在他的童年时期,两名亲密接触者因麻风病而接受治疗。组织病理学检查显示在Ziehl-Neelsen染色中有抗酸杆菌浸润的组织细胞。裂口皮肤和鼻腔涂片显示出许多耐酸杆菌。临床,流行病学,组织病理学和微生物学特征之间的相关性可以诊断出麻风病的麻风,组蛋白变体。根据世界卫生组织的建议,开始了多药治疗。看到了快速而持续的改善。组织状麻风病是麻风病的一种罕见表现,韦德于1960年首次描述。此后很少有病例报告,其中大多数来自该病高发国家。早期识别和治疗对于预防神经功能障碍和实现流行病学控制至关重要。

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