Results 21 to 30 of about 1,885 (186)

Juvenile Granulosa Cell Tumor of the Ovary in Pregnancy: A Case Report [PDF]

open access: yesGynecology and Minimally Invasive Therapy
Juvenile-type granulosa cell tumors (JGCT) of the ovary are extremely rare. Most of them occur in premenarchal girls. The occurrence of JGCT in an adult, particularly during pregnancy, is very rare.
Kavita Khoiwal   +5 more
doaj   +2 more sources

Granulosa Cell Tumour – A Rare Presentation at Age Twenty

open access: yesPakistan 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   +3 more sources

Juvenile Granulosa Cell Tumor Mimicking HAIR-AN in a 4-year-old: A Case Report [PDF]

open access: yesJCRPE
Predominantly androgen secreting juvenile granulosa cell tumors (JGCT) are uncommon and few reports have been published. We present a case of a JGCT that presented with signs of prepubertal hyperandrogenism and insulin resistance to highlight the ...
Rachel Choe Kim   +6 more
doaj   +2 more sources

JUVENILE GRANULOSA CELL TUMOR IN A 5 YEARS-OLD BULGARIAN GIRL PRESENTING WITH PRECOCIOUS PUBERTY: A CASE REPORT [PDF]

open access: yesJournal of IMAB
Ovarian tumors in children before puberty are rare and usually non-malignant. Granulosa cell tumors are rare sex cord-stromal tumors, accounting for 5% of all ovarian tumors and occur mainly in premenarchal girls and in women younger than 30 years.
Diana Hristova   +4 more
doaj   +2 more sources

Testicular juvenile granulosa cell tumor: a case report

open access: yesJournal of Ultrasound
The Testicular Juvenile Granulosa Cell Tumor (JGCT) is a rare testicular neoplasm that appears in the first months of life as a painless testicular mass. Following an accurate radiological ultrasound diagnosis, through which the cystic appearance of the lesion is observed, and histological confirmation, showing follicular growth pattern and an ...
Baldazzi M.   +12 more
core   +6 more sources

Pseudoprecocious puberty due to functional cystic juvenile granulosa cell tumor of the ovary in a 5-year-old girl

open access: yesJournal of Mahatma Gandhi Institute of Medical Sciences, 2016
A 5-year-old girl child presented with features of pseudoprecocious puberty in the form of bleeding per vaginum and bilateral breast enlargement since 10 days.
Shailaja Prabhala   +4 more
doaj   +2 more sources

A Case Report of Anaplastic Variant Juvenile Granulosa Cell Tumour [PDF]

open access: yesMajallah-i Zanān, Māmā̓ī va Nāzā̓ī-i Īrān, 2021
Introduction: Anaplastic variant of juvenile granulosa cell tumor is one of the rarest ovarian malignancies. The aim of this study is to describe a case of anaplastic variant ovarian granulosa cell tumor in a 14-year-old girl with presentation of ...
Masoumeh Gharib   +3 more
doaj   +1 more source

Juvenile granulosa cell tumor [PDF]

open access: yesAsian Journal of Oncology, 2016
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.
S. Rudra   +3 more
  +5 more sources

Granulosa-cell tumor after ovarian stimulation: A case report

open access: yesInternational Journal of Reproductive BioMedicine, 2018
Background: Ovarian superovulation and increased follicle-stimulating hormone concentration for infertility treatment may be the risk factors of developed granulosa-cell tumor.
Zohreh Yousefi   +7 more
doaj   +1 more source

Mixed sex cord–stromal tumor (gynandroblastoma) with malignant morphology involving both ovaries: a case report

open access: yesJournal of International Medical Research, 2023
Mixed sex cord–stromal tumors, which consist of poorly differentiated Sertoli cells and Leydig cells and juvenile granulosa cell tumor tissue, are extremely rare.
Bayan Maraqa   +4 more
doaj   +1 more source

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