Meigs’ syndrome and adult-type granulosa cell tumor

Objective: Adult-type granulosa cell tumors (GCT) are sex cord-stromal tumors and often accompanied with abdominal distention and hyperestrogenism-related symptoms. Adult-type GCT-presenting ascites and pleural effusion is extremely rare. Case report: A 56-year-old perimenopausal woman presented wit...

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Autores principales: Szu-Ting Yang, Min Cheng, Chung-Ru Lai, Shu-Huei Shen, Wen-Ling Lee, Peng-Hui Wang
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/9ee708e3d45d40be9457181ed6c17573
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spelling oai:doaj.org-article:9ee708e3d45d40be9457181ed6c175732021-11-18T04:44:51ZMeigs’ syndrome and adult-type granulosa cell tumor1028-455910.1016/j.tjog.2021.09.028https://doaj.org/article/9ee708e3d45d40be9457181ed6c175732021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S1028455921002680https://doaj.org/toc/1028-4559Objective: Adult-type granulosa cell tumors (GCT) are sex cord-stromal tumors and often accompanied with abdominal distention and hyperestrogenism-related symptoms. Adult-type GCT-presenting ascites and pleural effusion is extremely rare. Case report: A 56-year-old perimenopausal woman presented with abdominal distention and abnormal vaginal spotting. Ultrasound and abdominal computed tomography showed a complex cystic mass in the left ovary accompanied with bilateral pleural effusion and ascites. The patient underwent total abdominal hysterectomy, bilateral salpingo-oophorectomy, left pelvic lymph node dissection, omentectomy and appendectomy. Final histopathological diagnosis was adult-type GCT. The patient had postoperative hormone and anti-angiogenesis agent therapy with free of disease. Conclusion: Ovarian cystic complex mass accompanied with ascites and pleural effusion often results from malignant ovarian tumors or benign ovarian fibroma. Based on the aforementioned report, the rare types of ovarian tumors, such as adult-type granulosa cell tumor of the ovary should be taken into consideration.Szu-Ting YangMin ChengChung-Ru LaiShu-Huei ShenWen-Ling LeePeng-Hui WangElsevierarticleAdult granulosa cell tumorAscitesPleural effusionMeigs' syndromeGynecology and obstetricsRG1-991ENTaiwanese Journal of Obstetrics & Gynecology, Vol 60, Iss 6, Pp 1116-1120 (2021)
institution DOAJ
collection DOAJ
language EN
topic Adult granulosa cell tumor
Ascites
Pleural effusion
Meigs' syndrome
Gynecology and obstetrics
RG1-991
spellingShingle Adult granulosa cell tumor
Ascites
Pleural effusion
Meigs' syndrome
Gynecology and obstetrics
RG1-991
Szu-Ting Yang
Min Cheng
Chung-Ru Lai
Shu-Huei Shen
Wen-Ling Lee
Peng-Hui Wang
Meigs’ syndrome and adult-type granulosa cell tumor
description Objective: Adult-type granulosa cell tumors (GCT) are sex cord-stromal tumors and often accompanied with abdominal distention and hyperestrogenism-related symptoms. Adult-type GCT-presenting ascites and pleural effusion is extremely rare. Case report: A 56-year-old perimenopausal woman presented with abdominal distention and abnormal vaginal spotting. Ultrasound and abdominal computed tomography showed a complex cystic mass in the left ovary accompanied with bilateral pleural effusion and ascites. The patient underwent total abdominal hysterectomy, bilateral salpingo-oophorectomy, left pelvic lymph node dissection, omentectomy and appendectomy. Final histopathological diagnosis was adult-type GCT. The patient had postoperative hormone and anti-angiogenesis agent therapy with free of disease. Conclusion: Ovarian cystic complex mass accompanied with ascites and pleural effusion often results from malignant ovarian tumors or benign ovarian fibroma. Based on the aforementioned report, the rare types of ovarian tumors, such as adult-type granulosa cell tumor of the ovary should be taken into consideration.
format article
author Szu-Ting Yang
Min Cheng
Chung-Ru Lai
Shu-Huei Shen
Wen-Ling Lee
Peng-Hui Wang
author_facet Szu-Ting Yang
Min Cheng
Chung-Ru Lai
Shu-Huei Shen
Wen-Ling Lee
Peng-Hui Wang
author_sort Szu-Ting Yang
title Meigs’ syndrome and adult-type granulosa cell tumor
title_short Meigs’ syndrome and adult-type granulosa cell tumor
title_full Meigs’ syndrome and adult-type granulosa cell tumor
title_fullStr Meigs’ syndrome and adult-type granulosa cell tumor
title_full_unstemmed Meigs’ syndrome and adult-type granulosa cell tumor
title_sort meigs’ syndrome and adult-type granulosa cell tumor
publisher Elsevier
publishDate 2021
url https://doaj.org/article/9ee708e3d45d40be9457181ed6c17573
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AT chungrulai meigssyndromeandadulttypegranulosacelltumor
AT shuhueishen meigssyndromeandadulttypegranulosacelltumor
AT wenlinglee meigssyndromeandadulttypegranulosacelltumor
AT penghuiwang meigssyndromeandadulttypegranulosacelltumor
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