Bilal Mohammad, Kapetanos Anastasios, Khan Haider Ali, Thakkar Shyam
Allegheny General Hospital, 320 East North Avenue, Pittsburgh, PA, 15212, USA.
Center for Liver and Digestive Diseases, Holy Family Hospital, Satellite Town, Rawalpindi, 46000, Pakistan.
J Med Case Rep. 2015 May 23;9:118. doi: 10.1186/s13256-015-0594-8.
Dieulafoy's lesion is an uncommon but important cause of gastrointestinal bleeding in which hemorrhage occurs from a pinpoint, non-ulcerated arterial lesion. DLs are usually located in the stomach, most commonly in people between the ages of 50 and 70 years. In this report, we describe a teenage patient with an unusual presentation of a bleeding duodenal Dieulafoy's-like lesion that resembled the duodenal papilla.
An 18-year-old Pakistani woman presented to our emergency department with hematemesis of 6 hours' duration. Her past medical history was unremarkable. A nasogastric aspirate was negative for blood. The patient's hemoglobin was found to be 4 g/dl. She was resuscitated with intravenous fluids and blood transfusion. An esophagogastroduodenoscopy was performed, which revealed swelling in the first part of the duodenum, the initial appearance of which suggested that it was an abnormally placed or accessory papilla. There was a small, <3-mm opening on the lesion that resembled the biliary or pancreatic orifice. On gentle manipulation with a catheter, blood spurted from the swelling area, and a vessel was visible. Adrenaline was used for hemostasis. After hemostasis was achieved, it became clear that the lesion was most consistent with a Dieulafoy's-like lesion and not a papilla. Band ligation was then performed, and the patient did not develop any complications and did not have any further episodes of bleeding. The patient was eventually discharged to home in stable condition.
This case report highlights the importance of considering a DL as a cause of small-bowel hemorrhage and recognizing its potential resemblance to the papilla. Although the endoscopic diagnostic criteria for a Dieulafoy's lesion have been described in great detail, there is a paucity of literature describing a Dieulafoy's lesion or a similar lesion resembling the duodenal papilla.
Dieulafoy病是胃肠道出血的一个罕见但重要的病因,出血源于一个针尖样、无溃疡的动脉性病变。Dieulafoy病通常位于胃内,最常见于50至70岁的人群。在本报告中,我们描述了一名青少年患者,其十二指肠Dieulafoy样病变出血的表现不寻常,类似十二指肠乳头。
一名18岁的巴基斯坦女性因持续6小时的呕血症状就诊于我院急诊科。她既往病史无异常。鼻胃管抽吸物未发现血液。患者血红蛋白为4 g/dl。通过静脉输液和输血对她进行了复苏。随后进行了食管胃十二指肠镜检查,结果显示十二指肠第一部有肿胀,其最初外观提示为位置异常或副乳头。病变处有一个小于3毫米的小孔,类似胆管或胰管开口。用导管轻轻操作时,肿胀区域有血液喷出,可见一根血管。使用肾上腺素进行止血。止血成功后发现,该病变最符合Dieulafoy样病变而非乳头。随后进行了套扎术,患者未出现任何并发症,也未再有出血发作。患者最终病情稳定出院。
本病例报告强调了将Dieulafoy病视为小肠出血病因并认识到其可能与乳头相似的重要性。尽管已详细描述了Dieulafoy病的内镜诊断标准,但关于Dieulafoy病或类似十二指肠乳头的病变的文献却很少。