Literature DB >> 26522119

Malignant presentation of uterine lymphangioleiomyomatosis.

Dariusz Szpurek1, Sebastian Szubert2, Pawel Zielinski3, Andrzej Frankowski4, Stefan Sajdak1, Rafal Moszynski1.   

Abstract

OBJECTIVE: The main aim of this case report was to present the method of diagnosis, management, and the 12-year-follow-up of a patient diagnosed with primary uterine lymphangioleiomyomatosis (LAM). CASE REPORT: A 47-year-old woman was admitted to the Department of Thoracosurgery due to pulmonary lesions suspected to be metastatic. The potential primary site of the neoplasm was not identified by previous imaging studies and specialist counseling. The patient had a history of total abdominal hysterectomy without ovaries due to a uterine tumor recognized as cellular leiomyoma and left salpingo-oophorectomy due to a solid ovarian tumor also recognized as leiomyoma. She had previously undergone the removal of a left kidney angiomyolipoma. After histopathological examination of the pulmonary lesions and repeated evaluation of the ovarian and uterine tumors, the diagnosis of primary uterine LAM with metastases to the ovary and the lungs was established. Although new metastatic lesions occurred, the patient remained in good condition during the 12-year-follow-up.
CONCLUSION: The history of our patient and review of the literature suggest that although uterine LAM presents malignant features (i.e., metastasis), the disease is long lasting and the patient can be in good condition for a number of years.
Copyright © 2015. Published by Elsevier B.V.

Entities:  

Keywords:  genital track; lymphangioleiomyomatosis; metastasis; tuberous sclerosis; uterus

Mesh:

Year:  2015        PMID: 26522119     DOI: 10.1016/j.tjog.2015.08.015

Source DB:  PubMed          Journal:  Taiwan J Obstet Gynecol        ISSN: 1028-4559            Impact factor:   1.705


  5 in total

1.  Extrapulmonary uterine lymphangioleiomyomatosis (LAM) and dysfunctional uterine bleeding: the first presentation of LAM in a tuberous sclerosis complex patient.

Authors:  Lucy Grant; Saliya Chipwete; San Soo Hoo; Anjali Bhatnagar
Journal:  BMJ Case Rep       Date:  2019-02-25

2.  Unusual case of uterine intravascular leiomyomatosis with lymphatic spread to pelvic lymph nodes.

Authors:  Hanna Siatecka; Ramya P Masand
Journal:  Int J Clin Exp Pathol       Date:  2022-05-15

3.  Uterine PEComas: A Morphologic, Immunohistochemical, and Molecular Analysis of 32 Tumors.

Authors:  Jennifer A Bennett; Ana C Braga; Andre Pinto; Koen Van de Vijver; Kristine Cornejo; Anna Pesci; Lei Zhang; Vicente Morales-Oyarvide; Takako Kiyokawa; Gian Franco Zannoni; Joseph Carlson; Tomas Slavik; Carmen Tornos; Cristina R Antonescu; Esther Oliva
Journal:  Am J Surg Pathol       Date:  2018-10       Impact factor: 6.394

4.  Malignant perivascular epithelioid cell tumor in the female genital tract: Preferred reporting items for systematic reviews and meta-analyses.

Authors:  Chia-Hao Liu; Wei-Ting Chao; Shih-Chieh Lin; Hei-Yu Lau; Hua-Hsi Wu; Peng-Hui Wang
Journal:  Medicine (Baltimore)       Date:  2019-01       Impact factor: 1.889

5.  Pelvic Lymph Node Lymphangiomyomatosis Found During Surgery for Gynecological Fallopian Tube Cancer: A Case Report and Literature Review.

Authors:  Shan Xiao; Yijia Chen; Qianjue Tang; Lianwei Xu; Li Zhao; Zhenzhen Wang; Erkai Yu
Journal:  Front Med (Lausanne)       Date:  2022-07-15
  5 in total

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