1.Unicystic Granulosa Cell Tumor.
Nalli R SUMITRA DEVI ; Sathya Lakshmi RAMU ; Arun PRABHAKARAN ; Deepa Devi GOVINDASWAMY
Journal of Pathology and Translational Medicine 2015;49(2):167-170
No abstract available.
Granulosa Cell Tumor*
2.A case of bilateral granulosa cell tumors of both ovaries.
Bo Ok LEE ; Chang Qyun CHUNG ; Hyun Young BAE ; Jae Ho YOON ; Yong Hae PARK ; Ho Soon CHUNG
Korean Journal of Obstetrics and Gynecology 1992;35(8):1259-1263
No abstract available.
Female
;
Granulosa Cell Tumor*
;
Granulosa Cells*
;
Ovary*
3.Granulosa cell tumor of the ovary: time to launch a new prospective trial.
Journal of Gynecologic Oncology 2011;22(3):143-144
No abstract available.
Female
;
Granulosa Cell Tumor
;
Granulosa Cells
4.A Case of Precocious Pseudopuberty due to Granulosa Cell Tumor in an Infant.
Young Ran CHOI ; Youn Ha KANG ; Kyo Sun KIM ; Chang Hyo LEE
Journal of the Korean Pediatric Society 1983;26(8):835-839
No abstract available.
Female
;
Granulosa Cell Tumor*
;
Granulosa Cells*
;
Humans
;
Infant*
5.A case of granulosa cell tumor in pregnancy.
Hyun Chul CHO ; Sang Hee LEE ; Poong Gu LEE ; Jeong Gyu SHIN ; Won Jun CHOI ; Soon Ae LEE ; Jong Hak LEE ; Won Young PAIK
Korean Journal of Obstetrics and Gynecology 2002;45(7):1259-1262
Granulosa cell tumors of the ovary are rare, and account for 2 to 3% of ovarian tumors. Granulosa cell tumors are discovered often in perimenopausal or postmenopausal women but 10 to 26% are found in the reproductive age group. The tumors associated with pregnancy are infrequent. In this study, we present a case of granulosa cell tumor of left ovary at pregnancy.
Female
;
Granulosa Cell Tumor*
;
Granulosa Cells*
;
Humans
;
Ovary
;
Pregnancy*
6.Prolonged survival following maximal cytoreductive effort for peritoneal metastases from recurrent granulosa cell tumor of the ovary.
Terence C CHUA ; Narayan Gopalakrishna IYER ; Khee Chee SOO
Journal of Gynecologic Oncology 2011;22(3):214-217
No abstract available.
Female
;
Granulosa Cell Tumor
;
Granulosa Cells
;
Neoplasm Metastasis
;
Ovary
7.Adult Type Granulosa Cell Tumor of the Testis.
Dong Jun KIM ; Dong Woo SONG ; Sang Yeop YI ; Woon Yong YUN ; Tae Yung JEONG
Korean Journal of Urology 2008;49(1):95-97
Testicular granulosa cell tumor(GCT) is a rare neoplasm. We report here on an incidentally discovered testicular granulosa cell tumor in a 36-year-old man. The serum tumor markers were within the normal limits. The ultrasonographic findings revealed a mass with a heterogenous hypoechoic echotexture, including multiple variable sized cystic components. The histology on the orchiectomy specimen demonstrated a gonadal stromal tumor with granulosa cell features. Testicular granulosa cell tumor of the adult type is a very rare tumor, and there have been several isolated case reports and small serial studies described in the literature.
Adult
;
Female
;
Gonads
;
Granulosa Cell Tumor
;
Granulosa Cells
;
Humans
;
Orchiectomy
;
Testicular Neoplasms
;
Testis
;
Biomarkers, Tumor
8.Juvenile Granulosa Cell Tumor of Ovary in a Premenarcheal Girl.
Jong Hoon PARK ; Ki Heon AHN ; Dong Hyung LEE ; Ki Hyung KIM ; Man Soo YOON
Korean Journal of Obstetrics and Gynecology 2001;44(7):1324-1329
Granulosa cell tumors are rare in children, and less than 5% of all cases occur before puberty. In premenarcheal girls, the juvenile type of this tumor usually elicits the signs of sexual precocity. We have recently experienced a case of juvenile granulosa cell tumor of the ovary presented with sexual precocity. It is different from the adult granulosa cell tumor with regard to clinical and pathological features as well as biological behaviour as previously described by Scully. Only the clinical stage at the time of diagnosis is considered to be related to the prognosis. About 90% are diagnosed in early stage with a favorable prognosis. More advanced stage have a poor clinical outcome.
Adolescent
;
Adult
;
Child
;
Diagnosis
;
Female
;
Female*
;
Granulosa Cell Tumor*
;
Granulosa Cells*
;
Humans
;
Ovary*
;
Prognosis
;
Puberty
9.Adult granulosa cell tumor presenting with massive ascites, elevated CA-125 level, and low 18F-fluorodeoxyglucose uptake on positron emission tomography/computed tomography.
Ji Young TAK ; Gun Oh CHONG ; Ji Y PARK ; Seung Jeong LEE ; Yoon Hee LEE ; Dae Gy HONG
Obstetrics & Gynecology Science 2015;58(5):423-426
Adult granulosa cell tumors (AGCTs) presenting with massive ascites and elevated serum CA-125 levels have rarely been described in the literature. An ovarian mass, massive ascites, and elevated serum CA-125 levels in postmenopausal women generally suggest a malignant ovarian tumor, particularly advanced epithelial ovarian cancer. AGCT has low 18F-fluorodeoxyglucose uptake on positron emission tomography/computed tomography due to its low metabolic activity. In the present report, we describe a case of an AGCT with massive ascites, elevated serum CA-125 level, and low 18F-fluorodeoxyglucose uptake on positron emission tomography/computed tomography.
Adult*
;
Ascites*
;
Electrons*
;
Female
;
Granulosa Cell Tumor*
;
Granulosa Cells*
;
Humans
;
Ovarian Neoplasms
10.A Case of Hepatic Metastasis of Granulosa Cell Tumor of the Ovary.
Chang Ho CHO ; Ki Hyun PARK ; Bong Geun LEE ; Kyoung Bok LEE ; Ki Tae KIM ; Hyun Chan KIM
Korean Journal of Obstetrics and Gynecology 2001;44(12):2357-2361
Ovarian granulosa cell tumors are uncommon low-grade malignancies. They are characterized by their long history and their tendency to recur years after an apparent clinical cure. Only a small percentage of granulosa cell tumors metastasize, and they rarely do so to the liver. In this paper, we present a case of hepatic metastasis treated by surgery and BEP combination chemotherapy, with a brief review of corresponding literatures.
Drug Therapy, Combination
;
Female
;
Granulosa Cell Tumor*
;
Granulosa Cells*
;
Liver
;
Neoplasm Metastasis*
;
Ovary*