【孤立性网状组织细胞肉芽肿——附3例报告并文献复习】。

S Anaguchi, S Sinomiya, S Kinebuchi, M Kumakiri
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引用次数: 0

摘要

病例1为20岁男性,阴囊有结节。病例2为一名14岁女性,鼻上有一个红棕色的圆顶结节。病例3为30岁男性,前臂有一个红棕色的圆丘状结节。所有切除标本均表现为单发网状组织细胞肉芽肿的典型特征。真皮肿瘤巢内可见组织细胞和多核巨细胞。PAS反应和抗溶菌酶抗体染色呈阳性,S-100蛋白抗体染色呈阴性。为了明确网状组织细胞肉芽肿的分类学,我们回顾了多中心网状组织细胞增多症和成人黄色肉芽肿的文献。多中心网状组织细胞增多症被认为是一种全身性疾病,不同于孤立的网状组织细胞肉芽肿。然而,成人黄色肉芽肿与孤立的网状组织细胞肉芽肿表现出相似的临床特征,而不是组织病理特征的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Solitary reticulohistiocytic granuloma--a report of three cases and a review of literature].

Case 1 was a 20-year-old male with a nodule on the scrotum. Case 2 was a 14-year-old female with a dome-shaped, reddish-brown nodule on the nose. Case 3 was a 30-year-old male with a dome-shaped, reddish-brown nodule on the forearm. All of the excised specimens showed typical features of solitary reticulohistiocytic granuloma. There were histiocytes and multi-nucleated giant cells in the dermal tumorous nests. They were stained positively with PAS reaction and anti-lysozyme antibody, but were stained negatively with S-100 protein antibody. To clarify the nosology of the reticulohistiocytic granuloma, we reviewed the literatures of multicentric reticulohistiocytosis and adult xanthogranuloma. Multicentric reticulohistiocytosis was considered to be a systemic disease and different from solitary reticulohistiocytic granuloma. However, adult xanthogranuloma showed clinical similarities to solitary reticulohistiocytic granuloma instead of the differences in the histopathologic features.

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