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- W2050772853 abstract "In Brief BACKGROUND: Uterine arteriovenous malformations (AVMs) are extremely rare and can result in severe complications. Experience with diagnosis and management of these vascular malformations is very limited. CASE: We report on a patient with a history of nonmetastatic gestational trophoblastic disease. The patient developed a concomitant 4.4-cm intrauterine mass, suggestive of a molar pregnancy, during her second pregnancy. Despite suction and sharp curettage, the mass and menorrhagia persisted. After complex diagnostic imaging, the diagnosis of a uterine AVM was made. Subsequently, the patient underwent uterine arterial embolization and laparoscopic surgery to resect the mass. CONCLUSION: Because uterine AVMs are infrequently encountered, they initially may not be included in the differential diagnosis. The use of contemporary imaging, interventional radiology, and surgery can optimize patient outcome. Arteriovenous malformations are rarely identified in the uterus, and as a result, the differential diagnosis often is confounded." @default.
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- W2050772853 date "2008-08-01" @default.
- W2050772853 modified "2023-09-26" @default.
- W2050772853 title "Contemporary Diagnosis and Management of a Uterine Arteriovenous Malformation" @default.
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- W2050772853 doi "https://doi.org/10.1097/aog.0b013e3181719f7d" @default.
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