scholarly journals Occurrences of Dysgerminoma in the Left Ovary and of Granulosa-cell Tumor in the Right Ovary in a Japanese Black Cow

2003 ◽  
Vol 56 (9) ◽  
pp. 592-594
Author(s):  
Aya SHIBAHARA ◽  
Shunichi KAMIMURA ◽  
Takaaki ANDO ◽  
Hitomi KOIKE ◽  
Noriaki MIYOSHI ◽  
...  
Keyword(s):  
Granulosa Cell ◽  
Granulosa Cell Tumor ◽  
Cell Tumor ◽  
Left Ovary ◽  
The Right

scholarly journals Granulosa Cell Tumor In A Spayed Young Queen

2018 ◽  
Vol 69 (2) ◽  
pp. 1010
Author(s):  
Z. GÜNAY UÇMAK ◽  
M. UÇMAK ◽  
Ç. TEK ◽  
L. KOENHEMSI ◽  
Ö. ERDOGAN BAMAÇ ◽  
...  
Keyword(s):  
Granulosa Cell ◽  
Ovarian Tissue ◽  
Abdominal Mass ◽  
Granulosa Cell Tumor ◽  
Metastatic Potential ◽  
Cell Tumor ◽  
Obstetrics And Gynaecology ◽  
Young Queen ◽  
Internal Medicine Clinic ◽  
The Right

A four years old cat was presented to Clinic of Obstetrics and Gynaecology with complaints of weakness, inappetency, vomiting and estrus signs although it was spayed. Blood tests, radiography and ultrasonography revealed abdominal mass and uterine stump which were then removed surgically. Multilobular mass was defined as solid granulosa cell tumor (GCT). Increase of estrogen (E2) and insulin-like growth factor-1 (IGF-1) values were detected on the 10th postoperative day. On the 40th postoperative day, the cat was brought to Internal Medicine Clinic with the complaints of weakness, inappetency and cachexia. Anemia, leucocytosis, uremia, hyperglycemia, sensitiveness and pain in the right abdomen were determined. A tumor was detected in the liver by radiography and ultrasonography and was suspected to be GCT metastasis. Despite medical therapy, the cat died after four months. In conclusion; retained ovarian tissue after erroneous ovariohysterectomy may cause, regular estrus signs and GCT development. Even if GCTs are removed by surgical approach, they have metastatic potential that deteriorates the prognosis. Evaluating IGF-1 and E2 in the short postoperative term are beneficial for determining the metastatic potential of GCTs.

scholarly journals Ultrasound feature discordance in a bilateral juvenile ovarian granulosa cell tumor: A case report

2021 ◽  
Author(s):  
Li Zhang ◽  
Sheng Cai ◽  
Yahong Wang ◽  
Ying Wang ◽  
Zhitong Ge ◽  
...  
Keyword(s):  
Granulosa Cell ◽  
Granulosa Cell Tumor ◽  
Exploratory Laparotomy ◽  
Cell Tumor ◽  
Cystic Lesions ◽  
Ovarian Granulosa Cell ◽  
Ovarian Granulosa Cell Tumor ◽  
The Right ◽  
Cystic Masses

Abstract BackgroundAs a rare ovarian stromal tumor, the juvenile ovarian granulosa cell tumor (JGCT) is mainly seen in premenstrual and young women. It associates with high malignancy and recurrence rate, and early diagnosis and treatment could improve prognosis. Most cases are unilateral solid-cystic or solid masses, while unilocular cystic masses are rarely seen. As cystic ovarian tumors are often misdiagnosed as benign cystic lesions or functional cysts, cystic JGCT should not be overlooked.Case presentationWe report this special case of a 10-year-old female patient. It’s the first reported JGCT with completely inconsistent bilateral imaging manifestations, including an extremely rare unilocular cystic JGCT. A large solid-cystic JGCT appeared in her left ovary, and left adnexal resection was performed. A unilocular cyst occurred in the right ovary two years later. It was with a regular shape and smooth inner wall, mimicking a benign cyst. Since the patient was young and had the desire to preserve the right ovary, follow-up was initially recommended. However, the cyst size increased rapidly and exploratory laparotomy was finally performed. Pathology showed a unilocular cystic JGCT.ConclusionsAs cystic masses in young patients are easily misdiagnosed as benign or physiologic lesions, this case emphasizes the importance of postoperative follow-up for JGCTs. Exploratory laparotomy of persistent cystic lesions should be considered when necessary.

Granulosa Cell Tumour – A Rare Presentation at Age Twenty

2020 ◽  
Author(s):  
Munazza Anis
Keyword(s):  
Granulosa Cell ◽  
Tertiary Care ◽  
Granulosa Cell Tumor ◽  
Cell Tumor ◽  
Care Hospital ◽  
Age Group ◽  
Rare Presentation ◽  
Rare Type ◽  
Juvenile Granulosa Cell Tumor ◽  
The Right

Granulosa cell tumor is a rare type of ovarian tumor, which arises from sex cord stroma. Histologically this tumor has two types and is named according to the common age group they affect; adult granulosa cell tumor (AGCT) and juvenile granulosa cell tumor. AGCT constitutes 2-5% of all ovarian cancers. Mostly present in women of age > 40 years. In this case report, we discussed the role of conservative surgery in young adult reported with granulosa cell tumor. An unmarried teenage girl presented at a private tertiary care hospital with abdominal pain and abdominal distention. Radiological examinations suggested a mass originating from the right ovary for which laparotomy was done and a ruptured cyst was found near the right ovary with a mass adherent to surrounding peritoneal viscera. Right ovarian cystectomy along with omental biopsy and left ovarian biopsy was performed. Rare presentation of this tumor will help clinicians to not categorize the type histologically with the age group.

scholarly journals Incidental diagnosis of granulosa cell tumour in a 25-year-old woman

2021 ◽  
Vol 10 (3) ◽  
pp. 1202
Author(s):  
P. G. Paul ◽  
Sanghamitra Thakur ◽  
Anjana Annal ◽  
George Paul ◽  
K. Anusha Chowdary
Keyword(s):  
Granulosa Cell ◽  
Color Doppler ◽  
Granulosa Cell Tumor ◽  
Cell Tumor ◽  
Left Ovary ◽  
Inhibin B ◽  
Transvaginal Sonography ◽  
Solid Mass ◽  
Post Surgery ◽  
Intact Surface

A 25-year-old woman presented with backache of 2 weeks duration and had 45-60 days menstrual cycle. On transvaginal sonography (TVS), her left adnexa showed a heterogenous solid mass of 5.3×4.2 cm and moderate vascularity on color doppler. Serum inhibin B was raised to 2249 pg/ml. MRI showed 5.5× 4.5 cm solid mass in the left ovary with lobulated margins suggestive of sex cord-stromal/ germ cell tumor. Laparoscopy showed an enlarged left ovary with intact surface. Left adnexectomy with staging biopsies and infracolic omentectomy was performed. Histopathology showed adult granulosa cell tumor with intact ovarian capsule. One-month post-surgery, inhibin B level was 44 pg/ml. She wishes to conceive after six months follow-up. 

Postmenopausal hirsutism and hyperandrogenemia due to granulosa cell tumor of the ovary

2013 ◽  
Author(s):  
Cigdem Bahadir ◽  
Aysegul Atmaca ◽  
Hulusi Atmaca ◽  
Ramis Colak
Keyword(s):  
Granulosa Cell ◽  
Granulosa Cell Tumor ◽  
Cell Tumor

Granulosa cell tumor of the ovary

2017 ◽  
Vol 2 (16) ◽  
pp. 48
Author(s):  
D. Oprescu ◽  
C. Herghelegiu ◽  
A. Moldoveanu
Keyword(s):  
Granulosa Cell ◽  
Granulosa Cell Tumor ◽  
Cell Tumor

scholarly journals Right trisectionectomy for liver metastasis of granulosa cell tumor: a case report and literature review

2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Itsuki Koganezawa ◽  
Koichi Tomita ◽  
Masashi Nakagawa ◽  
Yosuke Ozawa ◽  
Toshimichi Kobayashi ◽  
...  
Keyword(s):  
Case Report ◽  
Liver Metastasis ◽  
Literature Review ◽  
Granulosa Cell ◽  
Granulosa Cell Tumor ◽  
Cell Tumor

scholarly journals Juvenile granulosa cell tumor

2016 ◽  
Author(s):  
Geetanjali Tuteja ◽  
S. Unmesh ◽  
S. Shree ◽  
S. Rudra ◽  
Keyword(s):  
Granulosa Cell ◽  
Precocious Puberty ◽  
Early Stage ◽  
Pubertal Development ◽  
Granulosa Cell Tumor ◽  
Cell Tumor ◽  
Cell Tumour ◽  
Tumour Resection ◽  
Granulosa Cell Tumour ◽  
Juvenile Granulosa Cell Tumor

The differential diagnosis for precocious puberty in a young female includes peripheral causes. This case report documents a rare cause of isosexual precocious puberty, a juvenile granulosa cell tumour of the ovary–and a brief literature review. A one year-old baby girl presented with mass abdomen, vaginal discharge and rapid onset of pubertal development. She underwent an exploratory laparotomy for tumour resection. Pathology reported a juvenile granulosa cell tumour of the ovary. Early stage granulosa cell tumor surgically treated has good prognosis. Adjuvant chemotherapy is not indicated in this setting.

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