青少年黄色肉芽肿病例报告及文献综述

S. Pradhan, Shuang Chen, Lin Xiong
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引用次数: 3

摘要

青少年黄色肉芽肿是一种罕见的,自限性皮肤病,尤其发生在婴儿,儿童晚期,很少发生在成人。它属于非朗格汉斯细胞组织细胞增多症的广泛组。它通常表现为单发或多发丘疹、斑疹或结节,直径几毫米,最常见的受累部位为头颈部,外阴少见。我们报告两例青少年黄色肉芽肿在一个18个月大的女性和18个月大的男性。4个月以来,女性外阴周围出现3个直径2-3毫米的黄色丘疹。同样,6个月以来,男性头部和前额出现多个直径3-4mm的棕橙色斑点。在这两个病例中,都进行了活检,但没有完全切除。临床及组织病理学检查证实为幼年型黄色肉芽肿。在儿童时期,幼年黄色肉芽肿是必要的,以区分与其他可能的鉴别诊断活检。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case Reports on Juvenile Xanthogranuloma and Brief Review of Literature
Juvenile xanthogranuloma is an unusual, self-limiting dermatological disorder occurring especially in infants, late childhood and rarely in adults. It belongs to the broad group of non-Langerhans cell histiocytosis. It usually appears as solitary or multiple papules, macules or nodules several millimeters in diameter with the head and neck being the most common site of involvement and vulva being the rare site. We report two cases of juvenile xanthogranuloma in an 18 months old female and 18 months old male. The female presented with three yellow papules measuring 2-3 mm in diameter around vulva region since 4 months. Similarly, the male presented with multiple tan-orange color macules on head and forehead measuring 3-4mm in diameter since 6 months. In both the cases, a biopsy without total excision was performed. The clinical and histopathological evaluation confirmed the diagnosis of juvenile xanthogranuloma. In childhood, juvenile xanthogranuloma is necessary to differentiate from another probable differential diagnosis by biopsy.
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