Results 31 to 40 of about 136,379 (287)
Familial Follicular-Cell Derived Carcinoma
Frontiers in Endocrinology, 2012 Follicular cell-derived well-differentiated thyroid cancer, papillary (PTC) and follicular thyroid carcinomas (FTC) compose 95% of all thyroid malignancies.
Eun Ju eSon, Vania eNosé
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Human Pathology: Case Reports, 2018 Germline mutations in the fumarate hydratase (FH) gene classically lead to Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) syndrome. Patients with HLRCC typically exhibit multiple cutaneous and uterine leiomyomas at a young age. They also display
Daniel R. Matson, M.D., Ph.D. +3 more
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Rare papillary renal neoplasm with reverse polarity: A case report and review of the literature
Frontiers in Oncology, 2023 Papillary renal neoplasm with reverse polarity (PRNRP) is a rare renal tumour and was newly named in 2019. This study reported a case of a 30-year-old female patient with a left renal tumour without any clinical symptoms and whose CT scan of her left ...
Xi Tu +4 more
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Indian Journal of Pathology and Microbiology, 2023 Xp11 translocation renal cell carcinoma (XPTRCC) is a very rare kidney neoplasm, which has been predominantly reported in young patients. Sarcomatoid transformation in renal cell carcinomas is known. However, its occurrence in XPTRCC is unreported so far
Rakhi V. Jagdale +3 more
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Three-gene risk model in papillary renal cell carcinoma: a robust likelihood-based survival analysis
Aging, 2020 Background: Papillary renal cell carcinoma (PRCC) accounts for 15% of all renal cell carcinomas. The molecular mechanisms of renal papillary cell carcinoma remain unclear, and treatments for advanced disease are limited.
Yutao Wang +12 more
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Papillary Renal Cell Carcinoma [PDF]
Journal of Diagnostic Medical Sonography, 1999 Papillary renal cell carcinoma comprises approximately 10% of all renal cell carcinomas. This subtype has a slower growth pattern, has less extensive involvement, and portends a better prognosis than do nonpapillary renal cell carcinomas. Papillary renal carcinomas tend to be avascular or hypovascular on ultrasound examination.
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Journal of Urological Surgery, 2018 We present a unique case of concurrent chromophobe, clear cell, and papillary renal cell carcinomas (RCC) in three separate sites in the same kidney after partial nephrectomy. We review the literature of synchronous RCC of up to two histologic subtypes,
Joan C. Delto +6 more
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EJNMMI Research, 2017 Background Despite the progress in the quality of multiphasic CT and MRI scans, it is still difficult to fully characterize a solid kidney lesion. Approximately 10% of all solid renal tumours turn out to be oncocytomas.
Antonios Tzortzakakis +5 more
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Hereditary papillary renal cell carcinoma
Seminars in Diagnostic PathologyHereditary papillary renal cell carcinoma (HPRCC) is an autosomal dominant syndrome characterized by the occurrence of bilateral and multifocal, classic type papillary renal cell carcinomas. In the recent decades, extensive molecular studies have narrowed the molecular underpinnings of this syndrome to missense mutations in tyrosine kinase domain of ...
Isa Mulingbayan Jacoba, Zhichun Lu
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Infectious Disease Reports, 2021 Neuropilin-1 (NRP1) is a recently identified glycoprotein that is an important host factor for SARS-CoV-2 infection. On the other hand, angiotensin-converting enzyme-2 (ACE2) acts as a receptor for SARS-CoV-2.
Md. Golzar Hossain +2 more
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