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An Extremely Rare Case of Disseminated Peritoneal Leiomyomatosis with a Pelvic Leiomyosarcoma and Omental Metastasis after Laparoscopic Morcellation: Systematic Review of the Literature
Minimally invasive treatment of uterine fibroids usually requires a power morcellation, which could be associated with several complications. A rare sequela is disseminated peritoneal leiomyomatosis. Indeed, recurrence or metastasis in these cases could be attributed to iatrogenic or under-evaluatio...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777378/ https://www.ncbi.nlm.nih.gov/pubmed/36553227 http://dx.doi.org/10.3390/diagnostics12123219 |
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author | Vimercati, Antonella Santarsiero, Carla Mariaflavia Esposito, Angela Putino, Carmela Malvasi, Antonio Damiani, Gianluca Raffaello Laganà, Antonio Simone Vitagliano, Amerigo Marinaccio, Marco Resta, Leonardo Cicinelli, Ettore Cazzato, Gerardo Cascardi, Eliano Dellino, Miriam |
author_facet | Vimercati, Antonella Santarsiero, Carla Mariaflavia Esposito, Angela Putino, Carmela Malvasi, Antonio Damiani, Gianluca Raffaello Laganà, Antonio Simone Vitagliano, Amerigo Marinaccio, Marco Resta, Leonardo Cicinelli, Ettore Cazzato, Gerardo Cascardi, Eliano Dellino, Miriam |
author_sort | Vimercati, Antonella |
collection | PubMed |
description | Minimally invasive treatment of uterine fibroids usually requires a power morcellation, which could be associated with several complications. A rare sequela is disseminated peritoneal leiomyomatosis. Indeed, recurrence or metastasis in these cases could be attributed to iatrogenic or under-evaluation of primary tumors, although a subset of cases is a sporadic sample of biological progression. We present an extremely rare case of a patient who underwent laparoscopic morcellation and after 12 years developed a pelvic leiomyosarcoma with two omental metastases, disseminated peritoneal leiomyomatosis with a parasite leiomyoma with bizarre nuclei and a parasite cellular leiomyoma simultaneously. The diagnosis was predicted preoperatively by an expert sonographer who recognized the ultrasound characteristics of uterine sarcoma and the localization of some of the masses, so the patient was referred to the gynaecological oncologists who could appropriately treat her. We present here a case report and a systematic review that could be a useful tool for further discussion and future clinical practice guidelines. |
format | Online Article Text |
id | pubmed-9777378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97773782022-12-23 An Extremely Rare Case of Disseminated Peritoneal Leiomyomatosis with a Pelvic Leiomyosarcoma and Omental Metastasis after Laparoscopic Morcellation: Systematic Review of the Literature Vimercati, Antonella Santarsiero, Carla Mariaflavia Esposito, Angela Putino, Carmela Malvasi, Antonio Damiani, Gianluca Raffaello Laganà, Antonio Simone Vitagliano, Amerigo Marinaccio, Marco Resta, Leonardo Cicinelli, Ettore Cazzato, Gerardo Cascardi, Eliano Dellino, Miriam Diagnostics (Basel) Case Report Minimally invasive treatment of uterine fibroids usually requires a power morcellation, which could be associated with several complications. A rare sequela is disseminated peritoneal leiomyomatosis. Indeed, recurrence or metastasis in these cases could be attributed to iatrogenic or under-evaluation of primary tumors, although a subset of cases is a sporadic sample of biological progression. We present an extremely rare case of a patient who underwent laparoscopic morcellation and after 12 years developed a pelvic leiomyosarcoma with two omental metastases, disseminated peritoneal leiomyomatosis with a parasite leiomyoma with bizarre nuclei and a parasite cellular leiomyoma simultaneously. The diagnosis was predicted preoperatively by an expert sonographer who recognized the ultrasound characteristics of uterine sarcoma and the localization of some of the masses, so the patient was referred to the gynaecological oncologists who could appropriately treat her. We present here a case report and a systematic review that could be a useful tool for further discussion and future clinical practice guidelines. MDPI 2022-12-19 /pmc/articles/PMC9777378/ /pubmed/36553227 http://dx.doi.org/10.3390/diagnostics12123219 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Vimercati, Antonella Santarsiero, Carla Mariaflavia Esposito, Angela Putino, Carmela Malvasi, Antonio Damiani, Gianluca Raffaello Laganà, Antonio Simone Vitagliano, Amerigo Marinaccio, Marco Resta, Leonardo Cicinelli, Ettore Cazzato, Gerardo Cascardi, Eliano Dellino, Miriam An Extremely Rare Case of Disseminated Peritoneal Leiomyomatosis with a Pelvic Leiomyosarcoma and Omental Metastasis after Laparoscopic Morcellation: Systematic Review of the Literature |
title | An Extremely Rare Case of Disseminated Peritoneal Leiomyomatosis with a Pelvic Leiomyosarcoma and Omental Metastasis after Laparoscopic Morcellation: Systematic Review of the Literature |
title_full | An Extremely Rare Case of Disseminated Peritoneal Leiomyomatosis with a Pelvic Leiomyosarcoma and Omental Metastasis after Laparoscopic Morcellation: Systematic Review of the Literature |
title_fullStr | An Extremely Rare Case of Disseminated Peritoneal Leiomyomatosis with a Pelvic Leiomyosarcoma and Omental Metastasis after Laparoscopic Morcellation: Systematic Review of the Literature |
title_full_unstemmed | An Extremely Rare Case of Disseminated Peritoneal Leiomyomatosis with a Pelvic Leiomyosarcoma and Omental Metastasis after Laparoscopic Morcellation: Systematic Review of the Literature |
title_short | An Extremely Rare Case of Disseminated Peritoneal Leiomyomatosis with a Pelvic Leiomyosarcoma and Omental Metastasis after Laparoscopic Morcellation: Systematic Review of the Literature |
title_sort | extremely rare case of disseminated peritoneal leiomyomatosis with a pelvic leiomyosarcoma and omental metastasis after laparoscopic morcellation: systematic review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777378/ https://www.ncbi.nlm.nih.gov/pubmed/36553227 http://dx.doi.org/10.3390/diagnostics12123219 |
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