Acquired Hemophilia A with Gastrointestinal Bleeding

被引:6
|
作者
Park, Narae [1 ]
Jang, Jin Seok [1 ]
Cha, Jae Hwang [1 ]
机构
[1] Dong A Univ, Coll Med, Dept Internal Med, Div Gastroenterol, Busan, South Korea
关键词
Acquired; Factor VIII deficiency; Gastrointestinal hemorrhage; Hemophilia A; PEPTIC-ULCER; EPIDEMIOLOGY; HEMORRHAGE; DIAGNOSIS; METAANALYSIS;
D O I
10.5946/ce.2019.036
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Peptic ulcer disease is the most common cause of acute gastrointestinal bleeding, followed by variceal bleeding, Mallory-Weiss syndrome, and malignancy. On the contrary, acquired hemophilia A is a very rare hemorrhagic disease, which usually manifests with nusculocutaneous bleeding, caused by autoantibodies against coagulation factor VIII. A 78-year-old man presented to the Emergency Department with melena. Dieulafoy's lesions were observed on esophagogastroduodenoscopy, and endoscopic cauterization was performed. However, the patient complained of back pain and symptoms indicative of upper gastrointestinal bleeding. Abdominopelvic computed tomography was performed, and hematoma in the psoas muscle was detected. Antibodies against coagulation factor VIII were confirmed with a blood test, and the diagnosis of acquired hemophilia A was made. Here, we report a case of acquired hemophilia A presenting with upper gastrointestinal bleeding symptoms and present a brief review of literature.
引用
收藏
页码:90 / 93
页数:4
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