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获得性因子 VIII 抑制剂导致的结肠巨大壁内血肿

Giant Intramural Hematoma of the Colon in Acquired Factor VIII Inhibitor.

作者信息

Figueiredo Joana, Borges Nuno, Pascoalinho José, Matos Ricardo

机构信息

Department of General Surgery. Centro Hospitalar Universitário de Lisboa Central. Lisboa. Portugal.

出版信息

Acta Med Port. 2019 Sep 2;32(9):614-617. doi: 10.20344/amp.8519.

Abstract

Intramural hematoma of the colon is very rare, particularly when associated with the development of autoantibodies against factor VIII.We report a case of a 66-year-old man with abdominal pain, hematochezia and clots in the left colon, without any radiologic signs of active bleeding or bowel occlusion or analytical changes in routine coagulation screening, but with positive autoantibodies against factor VIII. The clinical instability prompted surgical exploration. An intramural hematoma of the left colon was found, and a left colectomy was performed. The patient was treated with hemoderivatives and corticosteroids with clinical improvement. The diagnosis of spontaneous intramural hematoma might be a challenge, particularly in the absence of clinical suspicion. An early recognition is essential for a positive outcome. This case highlights a rare cause of bleeding and intestinal obstruction, but also the difficulty and relevance of establishing a clinical diagnosis when diagnostic tests are not completely informative.

摘要

结肠壁内血肿非常罕见,尤其是与抗凝血因子VIII自身抗体的产生相关时。我们报告一例66岁男性病例,该患者有腹痛、便血及左半结肠血凝块,在常规凝血筛查中无任何活动性出血或肠梗阻的影像学征象或分析变化,但抗凝血因子VIII自身抗体呈阳性。临床不稳定促使进行手术探查。发现左半结肠壁内血肿,并实施了左半结肠切除术。患者接受血液制品和皮质类固醇治疗后临床症状改善。自发性壁内血肿的诊断可能具有挑战性,尤其是在缺乏临床怀疑的情况下。早期识别对于取得良好预后至关重要。该病例凸显了一种罕见的出血和肠梗阻原因,同时也表明当诊断检查信息不完全时建立临床诊断的难度和重要性。

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