A rare case of purely cutaneous Rosai–Dorfman’s disease: Xanthoma-like presentation

Sushanti Jadhav, A. Dongre, B. Darkase, Ameet L. Dandale
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Abstract

Rosai–Dorfman’s disease (RDD) is sinus histiocytosis with massive lymphadenopathy. Cutaneous RDD is a rare entity that presents with isolated skin involvement without any systemic involvement. We report a 35-year-old man with an asymptomatic large nodule on the preauricular region of the face with an irregular surface and multiple yellow studded nodules. On detailed physical and systemic examination, there was no lymph node or systemic involvement. Skin biopsy on histopathology showed dense dermal inflammatory infiltrate and foamy histiocytes with emperipolesis. Immunohistochemical markers were positive for S100 protein and CD68 protein but negative for CD1a. Thus, a diagnosis of cutaneous RDD was made.
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一例罕见的纯皮肤Rosai-Dorfman病:黄瘤样表现
Rosai-Dorfman病(RDD)是一种窦性组织细胞增生伴大量淋巴结病。皮肤RDD是一个罕见的实体,表现为孤立的皮肤受累而没有任何全身受累。我们报告一个35岁的男性,在脸的耳前区域有一个无症状的大结节,表面不规则,并有多个黄色点缀的结节。详细的体格和全身检查,没有淋巴结或全身受累。皮肤组织病理活检显示真皮炎症浸润,组织细胞呈泡沫状,并伴有表皮增生。免疫组化标记S100蛋白和CD68蛋白阳性,CD1a蛋白阴性。因此,诊断为皮肤RDD。
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