Phoon Nguyen Amanda, Firth Norman, Mougos Sophie, Kujan Omar
UWA Dental School, University of Western Australia, Nedlands, WA 6009, Australia.
Private Practice, OMFSurgery, Cambridge Street, Wembley, WA, Australia.
Case Rep Dent. 2018 Aug 29;2018:4162436. doi: 10.1155/2018/4162436. eCollection 2018.
An otherwise healthy 20-year-old male presented with an exophytic, polypoid, yellowish lesion involving the dorsal surface of his tongue, which he reported being present since birth and unchanged. This was removed by surgical excision and diagnosed as a leiomyomatous hamartoma. Histological examination revealed a combination of fibrovascular connective tissue, conspicuous smooth-muscle bundles, adipose tissue, minor salivary gland tissue, blood vessels, lymphoid tissue, peripheral nerves, and normal skeletal muscle. This case is exceptional due to the patient's age, as until now, lingual leiomyomatous hamartomas have been reported almost exclusively in a paediatric population. To our knowledge, this is the eldest age at which a LLH has been reported in the literature. This underscores the need for clinicians to consider this rarely reported entity when considering the radiographic and clinical differential diagnoses for these lesions, both in the paediatric and adult populations. We also present a review of the literature regarding lingual leiomyomatous hamartomas.
一名20岁的健康男性,舌背出现一个外生性、息肉样、淡黄色病变,他称自出生以来就有且未发生变化。通过手术切除该病变,并诊断为平滑肌瘤性错构瘤。组织学检查显示,病变包含纤维血管结缔组织、明显的平滑肌束、脂肪组织、小唾液腺组织、血管、淋巴组织、周围神经和正常骨骼肌。该病例因患者年龄而特殊,因为迄今为止,舌部平滑肌瘤性错构瘤几乎仅在儿科人群中报道。据我们所知,这是文献中报道的舌部平滑肌瘤性错构瘤患者的最大年龄。这强调了临床医生在考虑儿科和成人患者这些病变的影像学和临床鉴别诊断时,需要考虑这种罕见报道的疾病。我们还对有关舌部平滑肌瘤性错构瘤的文献进行了综述。