Peritoneal Dissemination Complicating Morcellation of Uterine Mesenchymal Neoplasms

被引:182
作者
Seidman, Michael A. [1 ]
Oduyebo, Titilope [2 ]
Muto, Michael G. [2 ]
Crum, Christopher P. [1 ]
Nucci, Marisa R. [1 ]
Quade, Bradley J. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Div Womens & Perinatal Pathol, Sch Med,Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Brigham & Womens Hosp, Div Gynecol Oncol, Sch Med,Dept Obstet & Gynecol, Boston, MA 02115 USA
关键词
SUPRACERVICAL HYSTERECTOMY; LAPAROSCOPIC MYOMECTOMY; PARASITIC MYOMAS; LEIOMYOMATOSIS; LEIOMYOSARCOMA; MALIGNANCY; SURGERY; TISSUE;
D O I
10.1371/journal.pone.0050058
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: Power morcellation has become a common technique for the minimally invasive resection of uterine leiomyomas. This technique is associated with dissemination of cellular material throughout the peritoneum. When morcellated uterine tumors are unexpectedly found to be leiomyosarcomas or tumors with atypical features (atypical leiomyoma, smooth muscle tumor of uncertain malignant potential), there may be significant clinical consequences. This study was undertaken to determine the frequency and clinical consequence of intraperitoneal dissemination of these neoplasms. Methodology/Principal Findings: From 2005-2010, 1091 instances of uterine morcellation were identified at BWH. Unexpected diagnoses of leiomyoma variants or atypical and malignant smooth muscle tumors occurred in 1.2% of cases using power morcellation for uterine masses clinically presumed to be "fibroids" over this period, including one endometrial stromal sarcoma (ESS), one cellular leiomyoma (CL), six atypical leiomyomas (AL), three smooth muscle tumor of uncertain malignant potential (STUMPs), and one leiomyosarcoma (LMS). The rate of unexpected sarcoma after the laparoscopic morcellation procedure was 0.09%, 9-fold higher than the rate currently quoted to patients during pre-procedure briefing, and this rate may increase over time as diagnostically challenging or under-sampled tumors manifest their biological potential. Furthermore, when examining follow-up laparoscopies, both from in-house and consultation cases, disseminated disease occurred in 64.3% of all tumors (zero of one ESS, one of one CL, zero of one AL, four of four STUMPs, and four of seven LMS). Only disseminated leiomyosarcoma, however, was associated with mortality. Procedures are proposed for pathologic evaluation of morcellation specimens and associated follow-up specimens. Conclusions/Significance: While additional study is warranted, these data suggest uterine morcellation carries a risk of disseminating unexpected malignancy with apparent associated increase in mortality much higher than appreciated currently.
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