[A case of Farber's disease--histochemical, electron microscopic and biochemical studies].

S Hamanaka, A Hara, F Otsuka
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引用次数: 0

Abstract

A case of Farber's disease (disseminated lipogranulomatosis) is reported. A Japanese boy presented with progressive joint deformity, a hoarse voice, mental retardation and skin granulomatous lesions. He died of bronchopneumonia at the age of 2 years. Biopsied specimen from the perianal granulomatous lesion showed many macrophage contained lipids, and acidic oligo-, or polysaccharides, or, glycoconjugates. Electron microscopic study revealed, in addition to curvilinear tubular bodies (Farber's bodies), numerous granular structures accumulated in the cytoplasm of the macrophage. Biochemical analysis demonstrated a storage of free ceramide in the patient's liver, and confirmed the patient's diagnosis. This is the 5th case reported in Japan.

[法伯氏病1例——组织化学、电镜及生化研究]。
本文报告1例法伯氏病(弥散性脂肪肉芽肿病)。一个日本男孩表现为进行性关节畸形,声音沙哑,智力迟钝和皮肤肉芽肿病变。他在两岁时死于支气管肺炎。肛周肉芽肿病变的活检标本显示许多巨噬细胞含有脂质,酸性寡糖或多糖,或糖缀合物。电镜观察显示,巨噬细胞细胞质中除了有曲线状管状体(法伯氏体)外,还有大量颗粒状结构积聚。生化分析显示游离神经酰胺储存在患者的肝脏,并证实了患者的诊断。这是日本报告的第5例病例。
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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