Volume 201, Issue 6 , Pages 574.e1-574.e5, December 2009
Intravenous leiomyomatosis with intracardiac extension: a single-institution experience
Objective
The aim of this study was to outline the surgical management and outcomes for patients diagnosed with intravenous leiomyomatosis with intracardiac extension at a single institution.
Study Design
This was a retrospective review of patients diagnosed with intravenous leiomyomatosis with intracardiac extension between 2002–2008.
Results
Four patients were identified. The surgical approach in 3 (75%) patients was a single-stage operation. Four (100%) patients presented with cardiac symptoms: 3 (75%) with syncope and 1 (25%) with an abnormal electrocardiogram. Mean age at presentation was 48 years (range, 42–58 years). Complete resection of tumor was obtained in 1 (25%) patient and 3 (75%) patients experienced incomplete resection. Mean follow-up, including surveillance imaging, was 25.5 months (range, 8–57 months) and all 4 patients (100%) are currently free of recurrence.
Conclusion
Surgical excision remains an effective therapy for treating patients with benign metastasizing leiomyomatosis. Incomplete surgical resection may result in favorable response.
Key words: cardiac mass, fibroid, intravenous leiomyomatosis
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Reprints not available from the authors.
Film footage of the surgical procedure described in this article has been used to create a video abstract and was presented at the 57th Annual Clinical Meeting of the American College of Obstetricians and Gynecologists, Chicago, IL, May 2-6, 2009.
Cite this article as: Worley MJ Jr, Aelion A, Caputo TA, et al. Intravenous leiomyomatosis with intracardiac extension: a single-institution experience. Am J Obstet Gynecol 2009;201:574.e1-5.
PII: S0002-9378(09)00681-4
doi:10.1016/j.ajog.2009.06.037
© 2009 Published by Elsevier Inc.
Volume 201, Issue 6 , Pages 574.e1-574.e5, December 2009
