Results 31 to 40 of about 7,611 (271)
Diagnostics, 2020 This article reports a case of a 7-year-old girl with Turner syndrome, treated with growth hormone (GH), who developed ovarian dysgerminoma. The patient karyotype was mosaic for chromosome Xq deletion: 46,X,del(X)(q22)/45,X.
Ada Gawrychowska +6 more
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Advanced-Stage Gonadal Dysgerminoma in a Patient With a Previous Diagnosis of Familial Swyer Syndrome: A Very Rare Genetic Entity. [PDF]
Case Rep MedIntroduction Swyer syndrome is a genetic abnormality characterized by a 46,XY karyotype in a phenotypically female individual. Affected individuals typically have average or tall stature, unambiguous genitalia at birth, the presence of Müllerian structures, and bilateral streak gonads.
Oğlak SC +9 more
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Tumor Microenvironments in Malignant Ovarian Germ Cell Tumors: MHC Class I Loss and T-Cell Exhaustion in Dysgerminoma. [PDF]
Cancer SciMalignant ovarian germ cell tumor subtypes exhibit distinct tumor microenvironments. Dysgerminomas harbor abundant nonexhausted T cells, with progenitor exhausted T cells present in 60% of PD‐1–positive cases. However, MHC class I expression is lost across all analyzed subtypes, suggesting that restoring class I expression in dysgerminomas may enhance ...
Nakashima M +13 more
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Germ cell and other tumors in individuals with differences in sex development. [PDF]
CA Cancer J ClinAbstract Approximately one in 3500 to one in 5100 live‐born infants have atypical external genital development, known as differences in sex development (DSD). In 2005, an expert consensus conference thoroughly reviewed aspects of health care for individuals with DSD.
Witchel SF, Reyes-Múgica M.
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Ovarian dysgerminoma: clues to the radiological diagnosis
Diagnostic and Interventional Radiology, 2023 Ovarian dysgerminoma (OD) is a rare germ cell tumor accounting for 1%–2% of all malignant ovarian tumors and is generally associated with a good prognosis.
S. Amante, A. Félix, T. Cunha
semanticscholar +1 more source
Ovarian Dysgerminoma – Challenging Presurgical Diagnosis and Mini-Mally Invasive Treatment
Archives of Clinical and Medical Case Reports, 2023 Dysgerminoma is a rare malignant germ cell tumor of the ovary that often affects women in reproductive age. The presurgical differentiation of dysgerminoma from benign conditions is challenging. In early stages, malignant dysgerminoma can be treated with
Otto K +5 more
semanticscholar +1 more source
Unique combination of an ovarian dysgerminoma, streak ovary and uterine agenesis in a girl of 12 [PDF]
Archive of Oncology, 2008 Dysgerminoma of the ovary is a rare malignancy. It is common in dysegenetic ovaries. The prognosis is excellent if treated properly. This is a case report of a girl with agenesis of the uterus, streak ovary and dysgerminoma. Her external genitalia seemed
Dangal Ganesh
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Swyer Syndrome Presenting as Dysgerminoma: A Case Report
Journal of the ASEAN Federation of Endocrine Societies, 2023 Complete gonadal dysgenesis with 46,XY karyotype is a clinical condition characterized by the absence of testicular tissue but with the presence of typical Müllerian structures in a phenotypically female individual.
S. Tarenia +7 more
semanticscholar +1 more source
Imaging Findings in Dysgerminoma in a Case of 46 XY, Complete Gonadal Dysgenesis (Swyer syndrome) [PDF]
Journal of Clinical and Diagnostic Research, 2016 A 46 XY pure gonadal dysgenesis also known as Swyer syndrome. These patients are phenotypic females with normal female external genitalia and absent testicular tissue.
Pratiksha Yadav +2 more
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Cancer, 1978 A rare case of rapidly evolving dysgerminoma produced death by tumor in less than two months after onset of symptoms. It is important to recall that dysgerminoma possesses considerable malignant potential, which infrequently is manifested by rapidly progressive disease.
J J, Gillespie, L K, Arnold
openaire +2 more sources