Giant cystic degeneration of a uterine leiomyoma in a patient with autosomal dominant polycystic kidney disease
OBJECTIVETo report the management of a large uterine leiomyoma with diffuse cystic degeneration in a patient with autosomal dominant polycystic kidney disease (ADPKD). DESIGNCase Report. SETTINGCleveland Clinic Florida, Department of Gynecology, Section of Minimally Invasive Gynecologic surgery, Wes...
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Published in: | Case reports in women's health Vol. 10; pp. 1 - 3 |
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Main Authors: | , , , , , |
Format: | Report |
Language: | English |
Published: |
01-04-2016
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Online Access: | Get full text |
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Summary: | OBJECTIVETo report the management of a large uterine leiomyoma with diffuse cystic degeneration in a patient with autosomal dominant polycystic kidney disease (ADPKD). DESIGNCase Report. SETTINGCleveland Clinic Florida, Department of Gynecology, Section of Minimally Invasive Gynecologic surgery, Weston Florida. PATIENTSA 52-year old woman with ADPKD with a large abdominal mass, abnormal uterine bleeding and symptomatic anemia. Imaging revealed a giant intramural cystic lesion of the uterus compressing the inferior vena cava. INTERVENTIONSUterine artery embolization and blood transfusion followed by a computed tomography guided cyst aspiration were performed on admission to alleviate anemia and abdominal pain and distension. Total laparoscopic hysterectomy with bilateral salpingectomy was performed in an outpatient setting. MAIN OUTCOME MEASURESManagement of large cystic degeneration of leiomyoma. RESULTSNormal recovery from definitive surgery. Surgical pathology confirmed a benign, cystically dilated leiomyoma. CONCLUSIONThis case demonstrates the management of giant intramural cyst lesion of the uterus using a minimally invasive surgical approach, as opposed to emergency surgery via laparotomy. CAPSULELarge uterine leiomyoma with diffuse cystic degeneration in a patient with autosomal dominant polycystic kidney disease, in which step-wise treatments allows successful minimally invasive hysterectomy. |
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Bibliography: | ObjectType-Case Study-2 content type line 59 SourceType-Reports-1 ObjectType-Report-1 |
ISSN: | 2214-9112 |
DOI: | 10.1016/j.crwh.2016.04.001 |