Results 81 to 90 of about 7,453 (264)
Frontiers in Endocrinology, 2022 17α−hydroxylase/17,20−lyase deficiency (17-OHD), caused by mutations in the gene of the cytochrome P450 family 17 subfamily A member 1 (CYP17A1), is a rare type of congenital adrenal hyperplasia (CAH), usually characterized by cortisol and sex steroid ...
Min Yin +3 more
doaj +1 more source
46, XY complete gonadal dysgenesis with pubertal virilisation due to dysgerminoma/gonadoblastoma
BMJ Case Reports, 2020 Complete gonadal dysgenesis (CGD) or Swyer syndrome is characterised by sexual infantilism in a phenotypic female with 46, XY karyotype. Patients with gonadal dysgenesis and Y-chromosome material are at a high risk of developing gonadoblastoma and ...
S. Alam +3 more
semanticscholar +1 more source
Cromossomo Y na síndrome de Turner: revisão da literatura [PDF]
, 2009 Turner syndrome (TS) is one of the most common types of aneuploidy among humans, and is present in 1:2000 newborns with female phenotype. Cytogenetically, the syndrome is characterized by sex chromosome monosomy (45,X), which is present in 50-60% of the ...
Bianco, Bianca Alves Vieira +5 more
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Langerhans' cell histiocytosis: Possible association with malignant germ cell tumour [PDF]
, 1995 A rare case of adult onset Langerhans' cell histiocytosis associated with dysgerminoma in a 35 year old Chinese woman is reported. The patient had a history of dysgerminoma of left ovary 15 years previously and had undergone surgery followed by ...
Lam, KY, Ng, IOL, Ng, WK
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Dysgerminoma in three patients with Swyer syndrome
World Journal of Surgical Oncology, 2007 Background Dysgerminoma is the most common malignant germ cell tumor of the ovary. This malignancy can be associated with pure gonadal dysgenesis or Swyer syndrome, mixed gonadal dysgenesis and partial gonadal dysgenesis.
Karimi Zarchi Mojgan, Behtash Nadereh
doaj +1 more source
Gynecology and Minimally Invasive Therapy, 2020 Ovarian diffuse large B-cell lymphoma (DLBCL) is rare. DLBCL is a complex type of lymphoma. The ovarian DLBCL usually harbor a favorable prognosis. We report a case of ovarian DLBCL that presented as an ovarian mass with lower abdominal pain and was ...
Pei-Chen Li, P. Lim, Y. Hsu, D. Ding
semanticscholar +1 more source
Malignant ovarian dysgerminoma in a 16-year-old leopard gecko (Eublepharis macularius)
Veterinární Medicína, 2023 The 16-year-old female leopard gecko (Eublepharis macularius) was presented with distended coelom and cachexia. Examination of the faecal sample ruled out the presence of protozoan parasites.
H Zborilova +5 more
doaj +1 more source
Germ cell and other tumors in individuals with differences in sex development
CA: A Cancer Journal for Clinicians, EarlyView.Abstract 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.
Selma Feldman Witchel +1 more
wiley +1 more source
Clinical Case Reports, Volume 13, Issue 10, October 2025.MRI of the pelvis with and without contrast performed 3 days prior to biopsy. Axial (A) and sagittal (B) T2 weighted MRI of the anterior abdominal mass demonstrating heterogeneous T2 hyperintensity. Axial T1 (C) weighted image of the mass illustrates its relative T1 hypointensity.
Saurav Jha +3 more
wiley +1 more source
Classical gonadoblastoma: its relationship to the “dissecting” variant and undifferentiated gonadal tissue [PDF]
, 2017 Classical gonadoblastoma occurs almost entirely in the dysgenetic gonads of an individual who has a disorder of sex development. Approximately 40% of such neoplasms are bilateral.
Cheng, Liang, Roth, Lawrence M.
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