Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Oct 17;17(1):83.
doi: 10.1186/s13000-022-01258-9.

A case of death of patient with ovarian fibroma combined with Meigs Syndrome and literature review

Affiliations
Review

A case of death of patient with ovarian fibroma combined with Meigs Syndrome and literature review

Na Tan et al. Diagn Pathol. .

Abstract

Ovarian fibroma is the most common benign pure stromal tumor. It has no specific clinical manifestation, most of which are pelvic or adnexal masses. 10-15% of cases with hydrothorax or ascites, after tumor resection, hydrothorax and ascites disappear, known as Meigs Syndrome. The elevated level of CA125 in a few patients was easily misdiagnosed as ovarian malignant tumor. A case of bilateral Ovarian fibroma associated with Meigs Syndrome is reported and the literature is reviewed in order to improve the understanding of the changes and avoid misdiagnosis.

Keywords: Meigs Syndrome; Ovarian fibroma.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
A and B, CT coronal images through the 10th thoracic vertebrae and the pelvis demonstrate there were multiple irregular cystic and solid masses in bilateral adnexa (White small arrow). A large amount of effusion (white big arrowhead) is present within the bilateral thoracic cavity and pelvic and abdominal cavity. the uterus (circle 1), the bladder (circle 2)
Fig. 2
Fig. 2
Laparoscopic Intraoperative photograph, can be found bilateral ovarian fibroma (black cross) and ascites (black arrow)
Fig. 3
Fig. 3
A Histology: showed a large number of spindle cells or ovoid cells, Tumor cell nucleus is long fusiform. There is an obvious edema between cells (400×). B Immunohistochemistry: α-inhibin weakly positive (100×). C Immunohistochemistry: Vimentin positive (100×). D Immunohistochemistry: Reticular fiber positive (400×)

References

    1. Chung BM, Park SB, Lee JB, Park HJ, Kim YS, Oh YJ. Magnetic resonance imaging features of ovarian fibroma, fibrothecoma, and thecoma. Abdom Imaging. 2015;40(5):1263–72. doi: 10.1007/s00261-014-0257-z. - DOI - PubMed
    1. Chen YJ, Hsieh CS, Eng HL, Huang CC. Ovarian fibroma in a 7-month-old infant: a case report and review of the literature. Pediatr Surg Int. 2004;20(11–12):894–7. doi: 10.1007/s00383-004-1284-6. - DOI - PubMed
    1. Zhang Z, Wu Y, Gao J. CT diagnosis in the thecoma-fibroma group of the ovarian stromal tumors. Cell Biochem Biophys. 2015;71(2):937–43. doi: 10.1007/s12013-014-0288-7. - DOI - PubMed
    1. Hogan ME, Andreotti R. Ovarian Fibroma Presenting With Meigs Syndrome. Ultrasound Q. 2015;31(3):215–8. doi: 10.1097/RUQ.0000000000000144. - DOI - PubMed
    1. Numanoglu C, Kuru O, Sakinci M, Akbayır O, Ulker V. Ovarian fibroma/fibrothecoma: retrospective cohort study shows limited value of risk of malignancy index score. Aust N Z J Obstet Gynaecol. 2013;53(3):287–92. doi: 10.1111/ajo.12090. - DOI - PubMed

Supplementary concepts