J. D. Sharma, Upasana Kalita, Muktanjalee Deka, B. Bharadwaj, Adahra Patriesa Beso
{"title":"Juvenile granulosa cell tumor in a 35-year-old pregnant woman: A rare case report","authors":"J. D. Sharma, Upasana Kalita, Muktanjalee Deka, B. Bharadwaj, Adahra Patriesa Beso","doi":"10.32677/ijcr.v10i2.4357","DOIUrl":null,"url":null,"abstract":"Juvenile granulosa cell tumors (JGCTs) account for 5% of GCT and 3% are diagnosed after 30 years of age. JGCT is an uncommon neoplasm in pregnancy. About 90% are stage I at diagnosis but advanced-stage tumors are aggressive often resulting in recurrence or death within 3 years of diagnosis. We present a case of JGCT in a pregnant woman of 35 years old. The patient complained of sudden onset pain in her second trimester. Ultrasound whole abdomen was done and a malignant lesion was detected. Subsequently, the left ovarian cystectomy was performed and a diagnosis of JGCT was given which was confirmed by histopathology and immunohistochemistry.","PeriodicalId":13365,"journal":{"name":"Indian Journal of Case Reports","volume":"23 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32677/ijcr.v10i2.4357","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Juvenile granulosa cell tumors (JGCTs) account for 5% of GCT and 3% are diagnosed after 30 years of age. JGCT is an uncommon neoplasm in pregnancy. About 90% are stage I at diagnosis but advanced-stage tumors are aggressive often resulting in recurrence or death within 3 years of diagnosis. We present a case of JGCT in a pregnant woman of 35 years old. The patient complained of sudden onset pain in her second trimester. Ultrasound whole abdomen was done and a malignant lesion was detected. Subsequently, the left ovarian cystectomy was performed and a diagnosis of JGCT was given which was confirmed by histopathology and immunohistochemistry.