Results 41 to 50 of about 4,122 (198)
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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Pure ovarian dysgerminoma in a postmenopausal patient: A case report and review of the management
Gynecologic Oncology Reports, 2022 Background: A pure ovarian dysgerminoma in a postmenopausal female is a rare phenomenon. Case: A 65-year-old female presented with a large pelvic mass. Following surgical debulking, the patient was diagnosed with FIGO Stage IIB ovarian dysgerminoma.
Jennifer Vaz +8 more
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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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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
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Case Reports in Pathology, 2020 Ovarian dysgerminoma is a rare type of germ cell tumor. The majority of patient relapses occur within 2 years of diagnosis. Here, we report the case of a 74-year-old woman with a history of ovarian dysgerminoma 39 years earlier.
Yuichiro Sato +6 more
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Salvage resection of advanced mediastinal tumors [PDF]
, 2019 The surgical treatment of locally advanced mediastinal tumors invading the great vessels and other nearby structures still represent a tricky question, principally due to the technical complexity of the resective phase, the contingent need to carry out
Andreetti, Claudio +9 more
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JCRPE, 2022 Nijmegen breakage syndrome (NBS) is a rare autosomal recessive disease, affecting mainly patients of Slavic origin. It is caused by a defect in the NBN gene, resulting in defective nibrin protein formation.
Malgorzata A. Krawczyk +8 more
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Multiple primary malignancies and subtle mucocutaneous lesions associated with a novel PTENgene mutation in a patient with Cowden syndrome: Case report [PDF]
, 2011 Background Cowden syndrome (CS) is a cancer predisposition syndrome associated with increased risk of breast, thyroid, and endometrial cancers, and is characterized by development of benign mucocutaneous lesions.
Peter Vasovčák +3 more
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Inhibin immunoreactivity in gonadal and non-gonadal tumors [PDF]
, 1990 Inhibin immunoreactivity was estimated in a number of gonadal and non-gonadal tumors. Dog Sertoli cell tumors and human granulosa cell and Leydig cell tumors contained high concentrations of inhibin-like material.
Foekens, J.A. (John) +8 more
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Çocukluk çağı disgerminom tedavi sonuçları
Genel Tıp Dergisi, 2021 Amaç: Over disgerminomu tanısı ile izlenen hastaların demografik ve klinik özellikleri ile tedavi yaklaşımlarını geriye dönük olarak incelemektir. Gereç ve Yöntem: XXXXXX Üniversitesi Tıp Fakültesi Çocuk Onkoloji Bilim Dalı’nda, 2006-2020 yılları ...
Buket Kara +3 more
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