Results 11 to 20 of about 15,097 (214)
Adult‐type granulosa cell tumor: An unusual testicular tumor [PDF]
Clinical Case Reports, 2021 Adult type granulosa cell tumours are extremely rare. Albeit mostly benign, 10% have malignant potential associated with unfavorable pathological features.
Alain Mwamba Mukendi +3 more
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Meigs’ syndrome and adult-type granulosa cell tumor
Taiwanese Journal of Obstetrics & Gynecology, 2021 Objective: Adult-type granulosa cell tumors (GCT) are sex cord-stromal tumors and often accompanied with abdominal distention and hyperestrogenism-related symptoms. Adult-type GCT-presenting ascites and pleural effusion is extremely rare.
Szu-Ting Yang +5 more
doaj +3 more sources
Intraoperative scrape cytology: Adult granulosa cell tumor of ovary
Journal of Cytology, 2011 Adult granulosa cell tumor is often a hormonally active stromal cell neoplasm of the ovary with malignant potential. Intra-operative pathological assessment is a valuable tool in guiding optimal surgical treatment in patients.
Prabal Deb, Ajay Malik, Kavita K Sinha
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Testicular granulosa cell tumor, adult type
Indian Journal of Pathology and Microbiology, 2008 Granulosa cell tumor (GCT) of the adult type is a rare and slow-growing neoplasm in the testis. This tumor may be associated with endocrine manifestations and resemble classic GCT of the ovary morphologically. It has a potential for distant metastasis or
Gupta Anshu +3 more
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Cytomorphology of adult granulosa cell tumor in ascitic fluid
Indian Journal of Pathology and Microbiology, 2010 Adult granulosa cell tumors (AGCT) are associated with ascites in 10% of the cases. Although these tumors form two per cent of all ovarian tumors, they may create a diagnostic challenge in cytologic preparations.
Azad Kalpana, Khunger Jitender
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Juvenile Granulosa Cell Tumor of the Testis: A Preoperative Approach of the Diagnosis with Ultrasound [PDF]
Advanced Ultrasound in Diagnosis and Therapy, 2023 Granulosa cell tumor of the testis is a rare intermediate stromal cell tumor that can be distinguished in adult and juvenile type. The juvenile type is commonly presented in infants less than a year old-most often during the first 6 months of life and ...
Rodanthi Sfakiotaki, MS, Sergia Liasi, BM, Eleni Papaiakovou, BM, Irene Vraka, PhD, Marina Vakaki, PhD, Chrysoula Koumanidou, PhD
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Adult granulosa cell tumor with minor foci of juvenile granulosa cell tumor in postmenopausal woman: A rare case report. [PDF]
Int J Surg Case Rep, 2021 Granulosa cell tumor (GCT) is a rare neoplasm that is divided into adult GCT (AGCT) and juvenile GCT (JGCT). Generally, a patient will only have the AGCT or JGCT subtypes. Here, we presented the first case of AGTC accompanied by focal JGTC in a postmenopausal woman.A 63-year-old postmenopausal woman came with distended abdomen accompanied by ...
Rustamadji P +3 more
europepmc +3 more sources
Adult-type granulosa cell tumor of the testicle: case report
Research and Reports in Urology, 2019 Omar Halalsheh,1 Alia Al-Mohtaseb,2 Anas Ibrahim Al-Karasneh,3 Mustafa Mokhalad Al-Janabi,3 Amer Hussein Hallak41Department of Surgery and Urology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan; 2Department of Pathology,
Halalsheh O +4 more
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Granulosa Cell Tumour – A Rare Presentation at Age Twenty
Pakistan Journal of Medicine and Dentistry, 2020 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 ...
Munazza Ani +4 more
doaj +1 more source
Molecular manipulation of keratin 8/18 intermediate filaments: modulators of FAS-mediated death signaling in human ovarian granulosa tumor cells [PDF]
, 2016 Background: Granulosa cell tumors (GCT) are a rare ovarian neoplasm but prognosis is poor following recurrence. Keratin intermediate filaments expressed in these tumors are a diagnostic marker, yet paradoxically, may also constitute a target for ...
Davis, John S. +4 more
core +3 more sources