Qasim Abeer, Schmidt Patrik, Bhatt Tanushree, Itare Vikram, Ihimoyan Ariyo, Khaja Misbahuddin, Kandhi Sameer
Internal Medicine, BronxCare Health System, Bronx, USA.
Gastroenterology, BronxCare Health System, Bronx, USA.
Cureus. 2023 Jun 6;15(6):e40050. doi: 10.7759/cureus.40050. eCollection 2023 Jun.
Dieulafoy's lesion (DL) is an unusual cause of recurrent gastrointestinal bleeding that can be fatal. It can occur in various parts of the gastrointestinal (GI) tract, most commonly located in the stomach, especially at the level of lesser curvature; however, it can occur in other parts, including the colon, esophagus, and duodenum. A duodenal Dieulafoy lesion is characterized by the presence of a larger-caliber artery that protrudes through the GI mucosa and can lead to massive hemorrhage. The exact cause of DL is yet to be determined. Clinical presentation includes painless upper GI bleeding, including melena, hematochezia, and hematemesis, or rarely iron deficiency anemia (IDA); however, most of the patients are asymptomatic. Some patients also have non-gastrointestinal comorbidities such as hypertension, diabetes, and chronic kidney disease (CKD). The diagnosis is established by esophagogastroduodenoscopy (EGD), which includes the presence of micro pulsatile streaming from a mucosal defect, the appearance of a fresh, densely adherent clot with a narrow point of attachment to a minute mucosal defect, and the visualization of a protruding vessel with or without bleeding. Initial EGD can be non-diagnostic due to the relatively small size of the lesion. Other diagnostic modalities include endoscopic ultrasound and mesenteric angiography. The treatment of duodenal DL includes thermal electrocoagulation, local epinephrine injection, sclerotherapy, banding, and hemoclipping. We present here a case of a 71-year-old female who had a history of severe IDA requiring multiple blood transfusions and intravenous iron in the past and was found to have duodenal DL.
迪厄拉富瓦病(DL)是复发性胃肠道出血的一种罕见病因,可能会致命。它可发生于胃肠道(GI)的各个部位,最常见于胃,尤其是胃小弯处;然而,它也可发生于其他部位,包括结肠、食管和十二指肠。十二指肠迪厄拉富瓦病的特征是存在一条较大口径的动脉穿过胃肠道黏膜,可导致大量出血。DL的确切病因尚未确定。临床表现包括无痛性上消化道出血,包括黑便、便血和呕血,或罕见的缺铁性贫血(IDA);然而,大多数患者无症状。一些患者还患有非胃肠道合并症,如高血压、糖尿病和慢性肾脏病(CKD)。通过食管胃十二指肠镜检查(EGD)确诊,其表现包括黏膜缺损处有微小搏动性血流、出现新鲜的、紧密附着的血凝块且附着点狭窄至微小黏膜缺损,以及可见突出的血管(有或无出血)。由于病变相对较小,初次EGD检查可能无法确诊。其他诊断方法包括内镜超声和肠系膜血管造影。十二指肠DL的治疗方法包括热凝术、局部肾上腺素注射、硬化疗法、套扎术和血管夹闭术。我们在此报告一例71岁女性病例,该患者既往有严重IDA病史,曾多次输血及静脉补铁,此次被发现患有十二指肠DL。