scholarly journals Megestrol activity in recurrent adult type granulosa cell tumour of the ovary

1997 ◽  
Vol 8 (8) ◽  
pp. 811-812 ◽  
Author(s):  
E. Briasoulis ◽  
V. Karavasilis ◽  
N. Pavlidis
2021 ◽  
Author(s):  
Jessica A. Pilsworth ◽  
Anne‐Laure Todeschini ◽  
Samantha J. Neilson ◽  
Dawn R. Cochrane ◽  
Daniel Lai ◽  
...  

2017 ◽  
Vol 13 (1) ◽  
pp. 134-138 ◽  
Author(s):  
Vitaly Mezentsev ◽  
Hebah Ali ◽  
Jolanta McKenzie ◽  
Jaspal Virdi

2016 ◽  
Vol 14 (1) ◽  
pp. 44-49 ◽  
Author(s):  
Osama Al-Alao ◽  
Tawiz Gul ◽  
Ammar Al-Ani ◽  
Issam A. Bozom ◽  
Khalid Al-Jalham

2019 ◽  
Author(s):  
Ahmed Badran ◽  
Mahmoud A. Elshenawy ◽  
Hussein Soudy ◽  
Ayman Elshentenawy ◽  
Ahmed Mohieldin ◽  
...  

Abstract Background: Ovarian granulosa cell tumour is rare. This study aim is to report the clinical characteristics and long-term outcomes of adult-type OGCT (AOGCT) at King Faisal Specialist Hospital and Research Centre ( KFSH&RC) and to determine the prognostic factors affecting relapse and survival. we retrospectively reviewed patients with AOGCT, from 1988 to 2014, who were treated at our institution. Baseline characteristics, pathological findings, and outcomes were analysed, and reported. RESULTS: Sixty-one patients with AOGCT were identified with a median age of 49 years. Median follow-up was 5.0 years (range 2.1 -8.2 years). 74% of patients were FIGO stage I, whereas 7% stage II, 5% stage III and unknown in 14%. The most common presenting symptoms included abdominal pain (43%) and vaginal bleeding (43%). The majority of patients (38 patients, 62%) were treated with total abdominal hysterectomy and bilateral salpingo-oophorectomy. Five (8%) patients received adjuvant chemotherapy. Sixteen patients (26%) relapsed with a median time to relapse of 5.5 years (0.7-8.1 years). Half of the recurrences (8 patients, 50%) occurred after 5 years of diagnosis. Five-year overall survival and disease-free survival were 93% and 84%, respectively. Factors associated with high risk of recurrence were presence of ascites (p=0.000) and elevated preoperative CA 125 level (p=0.048). The overall survival was significantly influenced by the menopausal status (premenopausal 100% vs. postmenopausal 84%; p=0.02), preoperative CA 125 (normal 100% vs. elevated 64%; p=0.005), Ascites (present 33% vs. absent 100%; p=0.000), and age (<55 years 100% vs. ≥ 55 years 77%; p= 0.002). CONCLUSION: This study confirms a good outcome of patients with AOGCT. They require long-term follow-up because the recurrence can occur many years post the definitive therapy. The presence of ascites and elevated preoperative CA 125 levels were associated with a higher risk of recurrence and poor prognosis. The outcome seems not to be affected by fertility-sparing surgery and/or adjuvant chemotherapy.


2008 ◽  
Vol 61 (8) ◽  
pp. 914-919 ◽  
Author(s):  
E M Leuverink ◽  
B A Brennan ◽  
M L Crook ◽  
D A Doherty ◽  
I G Hammond ◽  
...  

2012 ◽  
Vol 62 (2) ◽  
pp. 257-266 ◽  
Author(s):  
Colin J R Stewart ◽  
Dorota Doherty ◽  
Rowan Guppy ◽  
Katherine Louwen ◽  
Yee C Leung

1960 ◽  
Vol XXXV (IV) ◽  
pp. 513-517
Author(s):  
W. P. Plate

ABSTRACT The hormone-producing mesenchymomas of the ovaries can be divided into androblastomas and gynaecoblastomas. The former are derived from »male« elements, and consist of Sertoli-cell tumours and Leydig-cell tumours. The latter arise from »female« elements and consist of granulosacell tumours and theca-cell tumours. Sertoli-cell tumours and granulosacell tumours produce oestrogens, while Leydig-cell tumours and theca-cell tumours produce oestrogens or androgens. Histologically, androblastomas and gynaecoblastomas are often difficult to distinguish. Since no »female« elements occur in a testicle, a granulosa-cell tumour in a testicle is improbable. Gynandroblastomas, therefore, can only be found in an ovary.


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