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Large leiomyomatosis peritonealis disseminata after laparoscopic myomectomy: A case report with literature review

INTRODUCTION: Leiomyomatosis peritonealis disseminata (LPD) is a rare disease in which multiple leiomyomas are formed intraperitoneally. Several LPD cases were associated with laparoscopic myomectomy using power morcellators; however, LPD with a large tumor size remains extremely rare. We present a...

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Autores principales: Yoshino, Yasunori, Yoshiki, Naoyuki, Nakamura, Reiko, Iwahara, Yuki, Ishikawa, Tomonori, Miyasaka, Naoyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725661/
https://www.ncbi.nlm.nih.gov/pubmed/33395914
http://dx.doi.org/10.1016/j.ijscr.2020.12.005
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author Yoshino, Yasunori
Yoshiki, Naoyuki
Nakamura, Reiko
Iwahara, Yuki
Ishikawa, Tomonori
Miyasaka, Naoyuki
author_facet Yoshino, Yasunori
Yoshiki, Naoyuki
Nakamura, Reiko
Iwahara, Yuki
Ishikawa, Tomonori
Miyasaka, Naoyuki
author_sort Yoshino, Yasunori
collection PubMed
description INTRODUCTION: Leiomyomatosis peritonealis disseminata (LPD) is a rare disease in which multiple leiomyomas are formed intraperitoneally. Several LPD cases were associated with laparoscopic myomectomy using power morcellators; however, LPD with a large tumor size remains extremely rare. We present a case of large LPD occurring after laparoscopic surgery. PRESENTATION OF CASE: A 26-year-old woman, gravida 0, underwent laparoscopic myomectomy with power morcellation in our institution. After 5 years, follow-up examination revealed pelvic tumors. Although we recommended resection, she refused and only wanted to be followed up. After 9 years from the first surgery, the tumors became symptomatic and were increasing in number (>10 nodules) and size (>15 cm). Needle biopsy detected leiomyoma. Computed tomography angiography showed that omental and mesenteric arteries were feeding the tumors. We performed laparotomy, and all the 19 tumors emerging from the omentum and mesenterium and weighing 7647 g in total were removed without injuring other organs. The maximum diameter of the largest tumor was 34 cm. The pathological diagnosis was nonmalignant LPD with leiomyoma. DISCUSSION: Among all reported cases, our case had the largest LPD size. The tumors reached such a huge size because of two possible reasons: (1) they gradually grew asymptomatically over a long period from the time of diagnosis, and (2) they were fed by particularly large vessels, including the omental and mesenteric arteries. CONCLUSION: A large LPD is not always symptomatic. After a laparoscopic myomectomy, especially with power morcellation, long-term follow-up is necessary to detect LPD.
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spelling pubmed-77256612020-12-13 Large leiomyomatosis peritonealis disseminata after laparoscopic myomectomy: A case report with literature review Yoshino, Yasunori Yoshiki, Naoyuki Nakamura, Reiko Iwahara, Yuki Ishikawa, Tomonori Miyasaka, Naoyuki Int J Surg Case Rep Case Report INTRODUCTION: Leiomyomatosis peritonealis disseminata (LPD) is a rare disease in which multiple leiomyomas are formed intraperitoneally. Several LPD cases were associated with laparoscopic myomectomy using power morcellators; however, LPD with a large tumor size remains extremely rare. We present a case of large LPD occurring after laparoscopic surgery. PRESENTATION OF CASE: A 26-year-old woman, gravida 0, underwent laparoscopic myomectomy with power morcellation in our institution. After 5 years, follow-up examination revealed pelvic tumors. Although we recommended resection, she refused and only wanted to be followed up. After 9 years from the first surgery, the tumors became symptomatic and were increasing in number (>10 nodules) and size (>15 cm). Needle biopsy detected leiomyoma. Computed tomography angiography showed that omental and mesenteric arteries were feeding the tumors. We performed laparotomy, and all the 19 tumors emerging from the omentum and mesenterium and weighing 7647 g in total were removed without injuring other organs. The maximum diameter of the largest tumor was 34 cm. The pathological diagnosis was nonmalignant LPD with leiomyoma. DISCUSSION: Among all reported cases, our case had the largest LPD size. The tumors reached such a huge size because of two possible reasons: (1) they gradually grew asymptomatically over a long period from the time of diagnosis, and (2) they were fed by particularly large vessels, including the omental and mesenteric arteries. CONCLUSION: A large LPD is not always symptomatic. After a laparoscopic myomectomy, especially with power morcellation, long-term follow-up is necessary to detect LPD. Elsevier 2020-12-03 /pmc/articles/PMC7725661/ /pubmed/33395914 http://dx.doi.org/10.1016/j.ijscr.2020.12.005 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Yoshino, Yasunori
Yoshiki, Naoyuki
Nakamura, Reiko
Iwahara, Yuki
Ishikawa, Tomonori
Miyasaka, Naoyuki
Large leiomyomatosis peritonealis disseminata after laparoscopic myomectomy: A case report with literature review
title Large leiomyomatosis peritonealis disseminata after laparoscopic myomectomy: A case report with literature review
title_full Large leiomyomatosis peritonealis disseminata after laparoscopic myomectomy: A case report with literature review
title_fullStr Large leiomyomatosis peritonealis disseminata after laparoscopic myomectomy: A case report with literature review
title_full_unstemmed Large leiomyomatosis peritonealis disseminata after laparoscopic myomectomy: A case report with literature review
title_short Large leiomyomatosis peritonealis disseminata after laparoscopic myomectomy: A case report with literature review
title_sort large leiomyomatosis peritonealis disseminata after laparoscopic myomectomy: a case report with literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725661/
https://www.ncbi.nlm.nih.gov/pubmed/33395914
http://dx.doi.org/10.1016/j.ijscr.2020.12.005
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