Lingual juvenile xanthogranuloma in a woman: a case report.
Lingual juvenile xanthogranuloma in a woman: a case report.
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女性中的舌幼年黄色神经瘤：病例报告。
DOI：
10.1186/1752-1947-5-30
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发表时间：
2011-01-24
影响因子：
1
通讯作者：
Villa F
中科院分区：
文献类型：
--
作者：
Villa A;Mariani U;Villa F
青少年黄色肉芽肿是一种罕见的非朗格汉斯细胞组织细胞增生症，通常发生在婴儿和儿童早期。存在单个或多个凸起的皮肤病变是这种自愈性疾病的特征。皮外部位罕见。我们提出了一个罕见的情况下，口腔青少年黄色肉芽肿在49岁的白人妇女。组织病理学诊断为组织细胞增生伴巨细胞，Touton型，符合青少年黄色肉芽肿。为了建立准确的诊断，显微镜检查和免疫组化染色是必要的。牙科医生，皮肤科医生和全科医生可能是第一个在口腔检查过程中认识到这种罕见情况的人。
Juvenile xanthogranuloma is a rare non-Langerhans cell histiocytosis that usually occurs during infancy and early childhood. The presence of single or multiple raised cutaneous lesions characterize this self-healing disorder. Extracutaneous sites are rare. We present a rare case of oral juvenile xanthogranuloma in a 49-year-old Caucasian woman. The histopathologic diagnosis of the lingual neoformation was histiocitary proliferation with the presence of giant cells, Touton type, compatible with juvenile xanthogranuloma. To establish an accurate diagnosis, microscopic evaluation and immunohistochemical staining are necessary. Dentists, dermatologists and general practitioners may be the first to recognize this rare condition during the inspection of the oral cavity.