Abstract:with Doppler evaluation is a good imaging modality for characterizing vascular lesions involving the wall of the gastrointestinal tract [5]. Bleeding from duodenal AVMs is extremely rare. This case is unique because of the characteristic appearance of the AVM on endoscopic ultrasound and the successful management by angioembolization.
“…Poon et al 3 reported a duodenal AVM in a 47‐year‐old man with melena which was initially misdiagnosed as a varix due to its appearance and the patient's history of alcoholism; the bleeding recurred after Histoacryl injection, and an AVM was diagnosed by angiography; surgical intervention was performed after embolization due to persistent melena and shock. Endoscopic ultrasonography and angiography may assist diagnosis, while angiography provides a vascular map that is essential for planning management 3,5 . AVMs are characterized by a large afferent artery, a racemose vascular network, and early venous drainage, as revealed by angiography in our case.…”
Section: Discussionmentioning
confidence: 69%
“…These treatments are less likely to be successful for large submucosal vessels; thus, surgical intervention is the mainstay of treatment 2–4 . However, treatment with endoscopic and angiographic methods seems to be acceptable in selected cases 5,6 . In our case, TAE was initially successful, but bleeding recurred 8 months later due to large and abundant blood vessels supplying the AVM.…”
Section: Discussionmentioning
confidence: 71%
“…Previously, the mainstay of treatment was surgical intervention. With the advantages of improving technology, definitive treatment by an endoscopic or angiographic method is possible 5,6 . In this article we present a patient with intermittent tarry stools secondary to a duodenal AVM which was revealed by angiography and initially treated by embolization but required surgical intervention 8 months after the procedure.…”
Arteriovenous malformations are a rare cause of gastrointestinal bleeding. Endoscopic examination can result in a variety of findings, and diagnosis and therapeutic management are uniquely challenging. We present an 83‐year‐old man with a history of hypertension and a 1‐month history of intermittent tarry stools. Esophagogastroduodenoscopy revealed one bulging mass with pulsation in the second portion of the duodenum which was confirmed as a duodenal arteriovenous malformation by angiography. The mass was initially embolized successfully, but subsequent surgical intervention was necessary due to recurrent bleeding eight months after the embolization. A relevant review of English medical literature was also performed in the text.
“…Poon et al 3 reported a duodenal AVM in a 47‐year‐old man with melena which was initially misdiagnosed as a varix due to its appearance and the patient's history of alcoholism; the bleeding recurred after Histoacryl injection, and an AVM was diagnosed by angiography; surgical intervention was performed after embolization due to persistent melena and shock. Endoscopic ultrasonography and angiography may assist diagnosis, while angiography provides a vascular map that is essential for planning management 3,5 . AVMs are characterized by a large afferent artery, a racemose vascular network, and early venous drainage, as revealed by angiography in our case.…”
Section: Discussionmentioning
confidence: 69%
“…These treatments are less likely to be successful for large submucosal vessels; thus, surgical intervention is the mainstay of treatment 2–4 . However, treatment with endoscopic and angiographic methods seems to be acceptable in selected cases 5,6 . In our case, TAE was initially successful, but bleeding recurred 8 months later due to large and abundant blood vessels supplying the AVM.…”
Section: Discussionmentioning
confidence: 71%
“…Previously, the mainstay of treatment was surgical intervention. With the advantages of improving technology, definitive treatment by an endoscopic or angiographic method is possible 5,6 . In this article we present a patient with intermittent tarry stools secondary to a duodenal AVM which was revealed by angiography and initially treated by embolization but required surgical intervention 8 months after the procedure.…”
Arteriovenous malformations are a rare cause of gastrointestinal bleeding. Endoscopic examination can result in a variety of findings, and diagnosis and therapeutic management are uniquely challenging. We present an 83‐year‐old man with a history of hypertension and a 1‐month history of intermittent tarry stools. Esophagogastroduodenoscopy revealed one bulging mass with pulsation in the second portion of the duodenum which was confirmed as a duodenal arteriovenous malformation by angiography. The mass was initially embolized successfully, but subsequent surgical intervention was necessary due to recurrent bleeding eight months after the embolization. A relevant review of English medical literature was also performed in the text.
Highlights
We report a rare case of small intestinal AVM.
Distinguishing small intestinal AVM is difficult.
Intravenous injection of ICG made the location and boundary more clear.
“…The patient has since not reported any further bleeding episodes and has remained stable with no requirement for iron infusions during a 10month follow-up period. Large duodenal AVMs are rare and previous case reports have described successful management of bleeding lesions with angiographic embolization [1,2] although this approach has not been universally effective [3], nor has laparoscopic ligation of the feeding branch of the gastroduodenal artery [3]. Band ligation has not been previously described but carries the risk of delayed bleeding from post-ligation ulcer development and glue injection has only provided temporary hemostasis in another case report [3].…”
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