کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4288985 | 1612105 | 2015 | 4 صفحه PDF | دانلود رایگان |
• Diffuse esophageal leiomyomatosis is frequently associated with Alport syndrome.
• Only curative option is esophagectomy.
• Misdiagnosis is common and workup should include endoscopic ultrasonography and 3D-gastric computed tomography for better anatomical delineation.
• Extensive imaging workup can result in better operative planning.
• Total esophagectomy should include all diseased tissue and provide good long term quality of life.
IntroductionDiffuse esophageal leiomyomatosis is a rare disease. Misdiagnosis is frequent and previous surgeries can complicate surgical management. The only treatment described for severe symptomatic cases is esophagectomy.Presentation of caseWe describe a case of diffuse esophageal leiomyomatosis associated with Alport syndrome in a 21 year-old female where endoscopic ultrasonography (EUS) with concomitant fluoroscopy and 3D-gastric computed tomography (3D-GCT) modified surgical management.DiscussionThe diagnosis of diffuse esophageal leiomyomatosis is difficult but can be greatly facilitated by extensive endoscopic and radiologic workup. Esophagectomy should only be entertained after complete anatomic mapping of the lesions, especially after previous surgeries.ConclusionEUS and 3D-GCT should strongly be considered as part of routine preoperative workup in these patients.
Journal: International Journal of Surgery Case Reports - Volume 10, 2015, Pages 183–186