Goldsmith P, Soames J V, Meikle D
National Hospital for Neurology & Neurosurgery, Queen Square, London.
J Laryngol Otol. 1995 Dec;109(12):1190-1. doi: 10.1017/s0022215100132402.
A case of a rare leiomyomatous hamartoma arising in the posterior tongue of a sixteen-month-old male is reported. There has been no recurrence following simple excision and presenting symptoms of choking on swallowing have resolved. Most other leiomyomatous hamartomas in the upper aerodigestive tract have been reported in Japanese patients and have involved the maxillary gingiva and hard palate.
报告了一例发生在一名16个月大男性舌后部的罕见平滑肌瘤性错构瘤病例。单纯切除后未复发，吞咽时窒息的症状已缓解。上呼吸道消化道的大多数其他平滑肌瘤性错构瘤病例报告来自日本患者，且病变累及上颌牙龈和硬腭。
