Multiple leiomyomatous hamartoma in the oral cavity
Multiple leiomyomatous hamartoma in the oral cavity
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DOI：
10.1111/j.1600-0714.2007.00518.x
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发表时间：
2007-04-01
影响因子：
3.3
通讯作者：
Kogo, Mikihiko
中科院分区：
文献类型：
--
作者：
Iida, Seiji;Kishino, Mitsunobu;Kogo, Mikihiko
平滑肌瘤性错构瘤是一种罕见的口腔先天性病变。在英文文献中，所有报告的病例均表现为牙槽嵴或舌部的孤立性病变，从未有报告显示此病变多次发生。一个相当罕见的情况下，多LH发生在一个2岁的日本男孩。在舌背有两个孤立的病灶，一个在后背呈息肉样肿块，另一个在前背呈小梭形隆起。组织学诊断均为LH。
Leiomyomatous hamartoma (LH) is congenital lesion rarely seen in oral cavity. In English literature, all reported cases appeared as solitary lesion in alveolar ridge or the tongue, and there have never been a report showing a case of multiple occurrence of this lesion. A quite rare case of multiple LH occurred in a 2-year-old Japanese boy is presented. A polypoid lesion was presented at incisive papilla and two isolated lesions in the tongue dorsum, one appeared as a polypoid mass in the posterior dorsum and other as a small spindle-shaped agger in the anterior dorsum. All of them were histologically diagnosed as LH.