Pujol J, Parés D, Mora L, Sans M, Jaurrieta E
Department of Surgery, Hospital Princeps d'Espanya, Ciutat Sanitaria i Universitària de Bellvitge, University of Barcelona, Hospitalet de Llobregat 08907, Barcelona, Spain.
Dis Esophagus. 2000;13(2):169-71. doi: 10.1046/j.1442-2050.2000.00107.x.
Diffuse leiomyomatosis of the oesophagus is a rare entity among oesophageal diseases. Histopathologically it is characterized by diffuse hypertrophy of the muscular layer extending to the whole oesophagus predominantly in the lower third, where it can result in tumour formation. Leiomyomatosis can involve the upper part of the stomach and is frequently associated with genital or tracheobronchial (bronchitracheal) muscular localizations. Also, it can be associated with Alport's syndrome in familial cases. For diagnosis, barium swallow, computerized tomography (CT) scan and, in recent years, endoscopic ultrasonography are used. Oesophageal resection is the only suitable treatment in symptomatic cases. We report three observations during 1979-95.
食管弥漫性平滑肌瘤病在食管疾病中是一种罕见的病症。组织病理学上,其特征为肌层弥漫性肥厚,主要累及食管下段,可延伸至整个食管,在此处可导致肿瘤形成。平滑肌瘤病可累及胃上部,常与生殖器或气管支气管(支气管气管)肌肉定位有关。此外,在家族性病例中,它可与阿尔波特综合征相关。诊断时,可采用吞钡检查、计算机断层扫描(CT),近年来也使用内镜超声检查。对于有症状的病例,食管切除术是唯一合适的治疗方法。我们报告了1979年至1995年间的三例观察病例。