2.Recurrent and Troublesome Variceal Bleeding from Parastomal Caput Medusae.
Claire STRAUSS ; Malathi SIVAKKOLUNTHU ; Abraham A AYANTUNDE
The Korean Journal of Gastroenterology 2014;64(5):290-293
Variceal bleeding is common in chronic liver disease and is a frequent cause of acute upper gastrointestinal bleeding. The most common site of varices is the lower oesophagus but they may occur at any location where there are portosystemic anastomoses and collateral vascular formation. Location of ectopic varices at the site of enterocutaneous stomas is rare. We report on three cases of recurrent and severe bleeding from parastomal varices, requiring hospital admission. The patients had chronic liver disease but of different aetiological factors. Variceal formation results from portal hypertension due to chronic liver disease. There are various treatment options for parastomal variceal bleeding, including local, medical, and surgical interventions. Management of parastomal variceal bleeding presents a recurring and difficult problem. Bleeding may be considerable and sometimes life threatening. This diagnosis must be considered in patients with chronic liver disease presenting with stomal bleeding, even where the variceal formation may not be readily visible.
Aged, 80 and over
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Chronic Disease
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Female
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*Gastrointestinal Hemorrhage
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Humans
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Liver Diseases/complications/*pathology
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Male
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Middle Aged
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Recurrence
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Severity of Illness Index
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Tomography, X-Ray Computed
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Varicose Veins/complications/*diagnosis
4.Recurrent Lower Gastrointestinal Bleeding from Congenital Arteriovenous Malformation in the Terminal Ileum Mimicking Intestinal Varicosis: A Case Report.
Jae Hee CHEON ; Ho June SONG ; Joo Sung KIM ; Kyu Joo PARK ; Woo Ho KIM ; Hyun Chae JUNG ; In Sung SONG
Journal of Korean Medical Science 2007;22(4):746-749
We report on an exceptional vascular cause of gastrointestinal hemorrhage. A 30-yr-old man was admitted because of recurrent hematochezia. Colonoscopy showed circumferential, erythematous, and nodular vascular distensions with hematocystic spots in the terminal ileum resembling varicosis and subsequent computed tomography with 3-dimensional angiographic reconstruction revealed a vascular architecture around the terminal ileum. No other potential source of bleeding was identified. The patient was treated by ileocecectomy and the final diagnosis was of an arteriovenous malformation confined to the terminal ileum. He has been followedup without a further hemorrhagic episode.
Adult
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Arteriovenous Malformations/complications/*pathology
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Diagnosis, Differential
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Gastrointestinal Hemorrhage/etiology/*pathology
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Humans
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Ileum/*abnormalities
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Intestines/*blood supply
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Male
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Recurrence
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Varicose Veins/etiology/*pathology
5.Jejunal Variceal Bleeding Successfully Treated with Percutaneous Coil Embolization.
So My KOO ; Soung Won JEONG ; Jae Young JANG ; Tae Hee LEE ; Seong Ran JEON ; Hyun Gun KIM ; Jin Oh KIM ; Yong Jae KIM
Journal of Korean Medical Science 2012;27(3):321-324
A 52-yr-old male with alcoholic liver cirrhosis was hospitalized for hematochezia. He had undergone small-bowel resection due to trauma 15 yr previously. Esophagogastroduodenoscopy showed grade 1 esophageal varices without bleeding. No bleeding lesion was seen on colonoscopy, but capsule endoscopy showed suspicious bleeding from angiodysplasia in the small bowel. After 2 weeks of conservative treatment, the hematochezia stopped. However, 1 week later, the patient was re-admitted with hematochezia and a hemoglobin level of 5.5 g/dL. Capsule endoscopy was performed again and showed active bleeding in the mid-jejunum. Abdominal computed tomography revealed a varix in the jejunal branch of the superior mesenteric vein. A direct portogram performed via the transhepatic route showed portosystemic collaterals at the distal jejunum. The patient underwent coil embolization of the superior mesenteric vein just above the portosystemic collaterals and was subsequently discharged without re-bleeding. At 8 months after discharge, his condition has remained stable, without further bleeding episodes.
Embolization, Therapeutic/*methods
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Gastrointestinal Hemorrhage/etiology/therapy
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Humans
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Jejunum/*blood supply
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Liver Cirrhosis, Alcoholic/complications
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Male
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Middle Aged
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Varicose Veins/diagnosis/etiology/*therapy
6.Involvement of Splenic Hemangioma and Rectal Varices in a Patient with Klippel - Trenaunay Syndrome.
Youn Jung CHOI ; Sam Ryong JEE ; Kwan Sik PARK ; Choong Heon RYU ; Hyo Rim SEO ; Seoung In HA ; Sang Heon LEE ; Kyung Sun OK
The Korean Journal of Gastroenterology 2011;58(3):157-161
Klippel - Trenaunay syndrome (KTS) is characterized by a cutaneous vascular nevus of the involved extremity, bone and soft tissue hypertrophy of the extremity and venous malformations. We present a case of KTS with splenic hemangiomas and rectal varices. A 29-year-old woman was referred for intermittent hematochezia for several years. She had history with a number of operations for cutaneous and soft tissue hamangiomas since the age of one year old and for increased circumference of her left thigh during the last few months. Abdominal CT revealed multiple hemangiomas in the spleen, fusiform aneurysmal dilatation of the deep veins and soft tissue hemangiomas. There was no evidence of hepatosplenomegaly or liver cirrhosis. Colonoscopy revealed hemangiomatous involvement in the rectum. There were rectal varices without evidence of active bleeding. Upon venography of the left leg, we also found infiltrative dilated superficial veins in the subcutaneous tissue and aneurysmal dilatation of the deep veins. The patient was finally diagnosed with KTS, and treated with oral iron supplementation only, which has been tolerable to date. Intervention or surgery is not required. When gastrointestinal varices or hemangiomatous mucosal changes are detected in a young patient without definite underlying cause, KTS should be considered.
Adult
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Colonoscopy
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Female
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Hemangioma/*complications
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Humans
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Iron, Dietary/therapeutic use
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Klippel-Trenaunay-Weber Syndrome/complications/*diagnosis/drug therapy
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Rectum/blood supply
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Spleen/blood supply
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Tomography, X-Ray Computed
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*Varicose Veins
7.Ruptured duodenal varices arising from the main portal vein successfully treated with endoscopic injection sclerotherapy: a case report.
Ha Yan KANG ; Won Kyung LEE ; Yong Hyun KIM ; Byung Woon KWON ; Myung Soo KANG ; Suk Bae KIM ; Il Han SONG
The Korean Journal of Hepatology 2011;17(2):152-156
Duodenal varices result from retroperitoneal portosystemic shunts that usually come from the pancreaticoduodenal vein and drain into the inferior vena cava. Because they are a rare but fatal cause of gastrointestinal bleeding, a prompt hemostatic intervention is mandatory. A 62-year-old man who had a history of excessive alcohol consumption presented with massive hematemesis and melena. Emergent endoscopy revealed ruptured varices with an adhering whitish fibrin clot on the postbulbar portion of the duodenum. Abdominal computed tomography demonstrated a cirrhotic liver with venous collaterals around the duodenum and extravasated contrast in the second and third portions. The collaterals originated from the main portal vein and drained via the right renal vein into the inferior vena cava. Endoscopic injection sclerotherapy with cyanoacrylate was successful in achieving hemostasis, and resulted in the near eradication of duodenal varices at a 6-month follow-up.
Cyanoacrylates/therapeutic use
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Duodenal Diseases/diagnosis/etiology/*therapy
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Duodenum/*blood supply
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Endoscopy, Gastrointestinal
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Gastrointestinal Hemorrhage/etiology/*therapy
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Humans
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Male
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Middle Aged
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Portal Vein
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Rupture
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Sclerosing Solutions/therapeutic use
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*Sclerotherapy
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Tomography, X-Ray Computed
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Varicose Veins/complications/*therapy
8.Clinical characteristics and outcomes of antenatal fetal intra-abdominal umbilical vein varix detection.
Si Won LEE ; Moon Young KIM ; Jung Eun KIM ; Jin Hoon CHUNG ; Hyun Jung LEE ; Ji Young YOON
Obstetrics & Gynecology Science 2014;57(3):181-186
OBJECTIVE: This study reviewed clinical characteristics of fetal intra-abdominal umbilical vein (FIUV) varices that were detected during antenatal ultrasound examinations. METHODS: Between January 2006 and January 2012, 121 cases of FIUV varices were detected and 7 cases were lost to follow-up. We retrospectively reviewed the medical records of 114 patients and neonates. RESULTS: From a total 96,553 ultrasound examinations in 43,995 pregnancies, 121 cases of FIUV varices were identified (2.8 per 1,000 pregnancies). Gestational age at diagnosis was 32.0 +/- 2.9 weeks (range, 20.1-36.3 weeks), the mean diameter of the FIUV varix was 12.6 +/- 2.1 mm (range, 8.0-21.0 mm) at initial diagnosis and the mean maximal diameter was 13.1 +/- 2.3 mm (range, 8.0-21.0 mm) during follow-up. The most severe pregnancy complications included one case of intrauterine fetal death and another case of fetal hydrops. Associated fetal anomalies (n = 11, 9.6%) detected by ultrasonography included bilateral renal pelvis dilatation, ventriculomegaly, cryptorchidism, incomplete renal duplication and pulmonary sequestration. A total of 104 cases (91.2%) were delivered at term and 10 cases (8.8%) were preterm deliveries before 37 weeks of gestation. CONCLUSION: FIUV varices that are not associated with fetal anomalies based on ultrasound examination during prenatal care have favorable pregnancy outcomes. Nevertheless, close fetal monitoring is recommended to decrease perinatal complications.
Bronchopulmonary Sequestration
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Cryptorchidism
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Diagnosis
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Dilatation
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Female
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Fetal Death
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Fetal Monitoring
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Follow-Up Studies
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Gestational Age
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Humans
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Hydrops Fetalis
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Infant, Newborn
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Kidney Pelvis
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Lost to Follow-Up
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Male
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Medical Records
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Pregnancy
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Pregnancy Complications
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Pregnancy Outcome
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Prenatal Care
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Retrospective Studies
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Ultrasonography
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Umbilical Veins*
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Varicose Veins*