Juvenile granulosa cell tumor in a 35-year-old pregnant woman: A rare case report

J. D. Sharma, Upasana Kalita, Muktanjalee Deka, B. Bharadwaj, Adahra Patriesa Beso
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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.
一名 35 岁孕妇的幼年颗粒细胞瘤:罕见病例报告
幼年颗粒细胞瘤(JGCT)占 GCT 的 5%,其中 3% 在 30 岁以后确诊。幼年颗粒细胞瘤在妊娠期是一种不常见的肿瘤。约 90% 的肿瘤在确诊时为 I 期,但晚期肿瘤具有侵袭性,通常会导致复发或在确诊后 3 年内死亡。我们报告了一例 35 岁孕妇的 JGCT 病例。患者主诉在怀孕后三个月突然出现疼痛。她接受了全腹超声波检查,发现了恶性病变。随后,进行了左侧卵巢囊肿切除术,并经组织病理学和免疫组化确诊为 JGCT。
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