AI Article Synopsis

  • Ovarian adult-type granulosa cell tumors are linked to endometrial hyperplasia and uterine cancer, as shown in a case involving a 65-year-old woman who had multiple curettages due to abnormal bleeding.
  • The patient underwent a laparoscopically-assisted vaginal hysterectomy after persistent vaginal bleeding, leading to the surprise discovery of an ovarian tumor during surgery.
  • Immunohistochemical analysis using various antibodies may provide insights into the tumor's molecular mechanisms, highlighting the need to consider rare ovarian tumors when dealing with recurrent vaginal bleeding and endometrial conditions.

Article Abstract

Ovarian adult-type granulosa cell tumors are often associated with endometrial hyperplasia or even uterine cancer. Herein, we present a case report of a 65-year-old female patient who had undergone curettage of the uterine cavity several times due to abnormal and irregular uterine bleeding. Owing to recurrent episodes of vaginal bleeding as well as ineffective pharmacological treatment of simple endometrial hyperplasia without atypia, the patient underwent a laparoscopically-assisted vaginal hysterectomy. Owing to an enlarged right ovary with bluish color, intra-operative pathological examination was immediately performed. Surprisingly, an ovarian adult-type granulosa cell tumor was diagnosed, and the surgery was extended to pelvic lymphadenectomy and omentectomy. Immunohistochemical staining with selected antibodies (Arginase 2, Nidogen 2, BAF250a/ARID1A, GPR30, SF-1/NR5A, and 1LRH-2E1/NR5A2) was also performed. In conclusion, in cases of recurrent vaginal bleeding concomitant with endometrial hyperplasia, the existence of rare ovarian tumors connected with extensive estrogenic stimulation must be taken into account. Immunostaining with selected antibodies (Arginase 2, Nidogen 2, ARID1A, or GPR30) may help elucidate the possible molecular mechanisms associated with the BAF250a/development of various ovarian/endometrial abnormalities.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607058PMC
http://dx.doi.org/10.1177/0300060519886984DOI Listing

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