Literature DB >> 3333004

Intracaval and intracardiac leiomyomatosis of uterine origin.

A Mazzola1, R Gregorini, B Procaccini, V Moretti, R Lucantoni, W Lorenzi, G Di Eusanio, M Colombati.   

Abstract

Intracaval leiomyomatosis of uterine origin is a rare disease. Extension to the right heart is exceptional. Based on the review of 11 cases reported in the literature and the case presented herein, which was treated successfully, the diagnostic and therapeutic problems are discussed. Diagnosis should be suggested when a female patient operated on previously for myofibroma of the uterus by hysterectomy, presents with a picture of cardiac myxoma. Diagnosis can be confirmed by iliocavogram and computerized tomography of the abdomen. Excision calls for a cardiac procedure under extracorporeal circulation and caval exploration which may be performed either simultaneously or as a two stage procedure.

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Year:  1986        PMID: 3333004     DOI: 10.1016/S0890-5096(06)60715-2

Source DB:  PubMed          Journal:  Ann Vasc Surg        ISSN: 0890-5096            Impact factor:   1.466


  4 in total

1.  Intravenous leiomyomatosis complicated by Budd-Chiari syndrome.

Authors:  B C Kuenen; P H Slee; C A Seldenrijk; S S Wagenaar
Journal:  Postgrad Med J       Date:  1996-11       Impact factor: 2.401

Review 2.  Intracaval and intracardiac leiomyomatosis of uterine origin.

Authors:  Cosmina Stoleriu; Kostas Rizas; Meinrad Gawaz; Tobias Geisler
Journal:  BMJ Case Rep       Date:  2013-11-05

Review 3.  Intracardiac leiomyomatosis: a comprehensive analysis of 194 cases.

Authors:  Bin Li; Xin Chen; Ya-Dong Chu; Ren-Yuan Li; Wei-Dong Li; Yi-Ming Ni
Journal:  Interact Cardiovasc Thorac Surg       Date:  2013-04-05

4.  Surgical treatment strategies for extra-pelvic intravenous leiomyomatosis.

Authors:  Hua Li; Jing Xu; Qiaowei Lin; Yong Zhang; Yun Zhao; Hanxing Tong; Ruiqin Tu; Demin Xu; Chunsheng Wang; Weiqi Lu
Journal:  Orphanet J Rare Dis       Date:  2020-06-16       Impact factor: 4.123

  4 in total

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