Results 11 to 20 of about 3,652 (213)

The association of enchondromatosis with malignant transformed chondrosarcoma and ovarian juvenile granulosa cell tumor (Ollier disease)

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2017
Objective: Ovarian juvenile granulosa cell tumor has an interesting association with multiple enchondromatosis (Ollier disease and Maffucci syndrome) and should be considered a leading diagnosis when an ovarian mass is found in young patients with these ...
Andrea Burgetova   +8 more
doaj   +3 more sources

Juvenile Granulosa Cell Tumor of the Testis: Prenatal Diagnosis and Management [PDF]

open access: yesEuropean Journal of Pediatric Surgery Reports, 2019
Prepubertal primary testicular tumors account for ∼1% of all pediatric solid tumors. We report a new case of prenatal diagnosis of juvenile-type granulosa cell tumor (JGCT).
Fabrizio Vatta   +6 more
doaj   +2 more sources

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

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 of the Testis: A Preoperative Approach of the Diagnosis with Ultrasound [PDF]

open access: yesAdvanced 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
doaj   +1 more source

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
openaire   +3 more sources

Ovarian Juvenile Granulosa Cell Tumor Case Report [PDF]

open access: yesJournal of Education and Teaching in Emergency Medicine, 2022
A 5-month-old female presented to the emergency department with worsening abdominal distention and postprandial emesis. Point-of-care ultrasound (POCUS) demonstrated extensive abdominal free fluid with a large, heterogeneous mass in the suprapubic region. This was confirmed on computed tomography (CT) of the abdomen and pelvis. The patient was urgently
Lemmons, Jasmine   +2 more
openaire   +4 more sources

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

Advances in non-germ cell tumours of the testis: focus on new molecular developments in sex cord-stromal tumours. [PDF]

open access: yesHistopathology
In this review, we summarise the major recent advances in Testicular Sex Cord‐Stromal Tumours, focusing on molecular alterations and biomarkers relevant for diagnosis, classification and prognosis. Testicular sex cord‐stromal tumours (TSCSTs) represent ~4%–8% of all testicular neoplasms.
Lobo J, Acosta AM.
europepmc   +2 more sources

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