一名3岁男孩舌部的肺泡软组织肉瘤：病例报告
Alveolar soft part sarcoma of the tongue in a 3-year-old boy: a case report.
作者信息
Noussios George, Chouridis Pantelis, Petropoulos Ioannis, Karagiannidis Kostas, Kontzoglou George
机构信息
ENT Department, (Street Konstantinoupoleos 49) Hippokratio General Hospital, Thessaloniki, Greece.
出版信息
J Med Case Rep. 2010 May 8;4:130. doi: 10.1186/1752-1947-4-130.
INTRODUCTION
Alveolar soft tissue sarcoma of the tongue is a very rare and aggressive tumor which occurs in infancy with a relatively controversial histogenesis. It may mimic benign vascular neoplasms and may metastasize to the lungs, brain or bones.
CASE PRESENTATION
We present the case of a three-year-old Caucasian boy who was admitted to our department with a history of dysphagia and two episodes of oral bleeding which had lasted for a period of six months. A thorough histological examination together with imaging techniques form the basis of a reliable diagnosis.
CONCLUSION
Alveolar soft tissue sarcoma of the tongue is a rare tumor which occurs in infancy and which is often misdiagnosed pre-operatively. It should therefore be included in the differential diagnosis of oral pediatric lesions.
引言
舌部肺泡软组织肉瘤是一种非常罕见且侵袭性强的肿瘤，发生于婴儿期，其组织发生相对存在争议。它可能类似良性血管肿瘤，并可能转移至肺、脑或骨骼。
病例报告
我们报告一例3岁白人男孩，因吞咽困难及两次口腔出血病史6个月入院。全面的组织学检查及影像学技术是可靠诊断的基础。
结论
舌部肺泡软组织肉瘤是一种发生于婴儿期的罕见肿瘤，术前常被误诊。因此，它应列入小儿口腔病变的鉴别诊断中。
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