Cooray Samantha, Dellaportas Dionysios, Caruana Clifford, Davies Andrew R
Department of Upper Gastrointestinal Surgery, St. Thomas' Hospital, Guy's and St. Thomas' Oesophago-Gastric Centre, London, UK.
Case Rep Surg. 2017;2017:4086056. doi: 10.1155/2017/4086056. Epub 2017 Feb 20.
. Spontaneous intramural oesophageal haematoma is a rare condition that usually occurs secondary to an acute or chronic coagulation disorder. The presenting complaint is often with retrosternal chest pain and most patients are initially investigated to exclude more common causes in the differential diagnosis, such as acute coronary syndromes. Severe life-threatening bleeding or perforation seldom, if ever, arises. . We present a case of spontaneous oesophageal haematoma which appears to have developed gradually in a 69-year-old female with uncontrolled hypertension and antiplatelet medication use. The diagnosis was made on computed tomography imaging and was further evaluated with upper gastrointestinal endoscopy. Management was conservative and a follow-up endoscopy two weeks later showed almost complete resolution of the lesion. . Spontaneous oesophageal haematomas are very rare and usually result in the separation of the mucosal layer from the underlying muscle, presenting with chest pain, haematemesis, and dysphagia. Usually the diagnosis is one of exclusion, based on computed tomography imaging and endoscopy. Conservative management is almost always successful.
自发性食管壁内血肿是一种罕见疾病,通常继发于急性或慢性凝血功能障碍。主要症状常为胸骨后胸痛,大多数患者最初接受检查以排除鉴别诊断中更常见的病因,如急性冠状动脉综合征。严重的危及生命的出血或穿孔极少发生。我们报告一例自发性食管血肿病例,该病例似乎在一名69岁患有未控制高血压且正在使用抗血小板药物的女性患者中逐渐发展。通过计算机断层扫描成像做出诊断,并通过上消化道内镜进行进一步评估。治疗采用保守治疗,两周后的随访内镜检查显示病变几乎完全消退。自发性食管血肿非常罕见,通常导致黏膜层与下层肌肉分离,表现为胸痛、呕血和吞咽困难。通常基于计算机断层扫描成像和内镜检查进行排除性诊断。保守治疗几乎总是成功的。