Juvenile xanthogranuloma of the tongue: A case report

IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
Ayumi Yamamoto, Sho Ishida, Yasuo Hanazawa
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引用次数: 0

Abstract

Juvenile xanthogranuloma (JXG) is a rare non-Langerhans cell histiocytosis that typically presents as a self-limiting dermatological condition in young children, and oral mucosal involvement is exceedingly rare. We report the case of a 2-year-old boy, in whom a pink exophytic nodule gradually enlarged for 3 months and subsequently changed to an orange submucosal mass in approximately 1 month. Excisional biopsy was performed to obtain a definitive diagnosis. Histopathological examination revealed diffuse proliferation of foamy histiocytes and Touton giant cells within the lesion. Based on these results, the patient was diagnosed with JXG. Herein, we present an uncommon case of oral JXG to increase awareness about this lesion. The patient is currently healthy, and no recurrence has been observed 2 years after surgical excision.
青少年舌黄色肉芽肿1例
青少年黄色肉芽肿(JXG)是一种罕见的非朗格汉斯细胞组织细胞增生症,通常在幼儿中表现为一种自限性皮肤病,口腔粘膜病变极为罕见。我们报告一个2岁男孩的病例,其中一个粉红色的外生性结节逐渐扩大了3个月,随后在大约1个月的时间里变成了一个橙色的粘膜下肿块。切除活检以获得明确的诊断。组织病理学检查显示病灶内泡沫组织细胞和图顿巨细胞弥漫性增生。根据这些结果,诊断为JXG。在此,我们提出了一个罕见的口腔JXG病例,以提高对这种病变的认识。患者目前健康,手术切除2年后未见复发。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
129
审稿时长
83 days
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