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of 306
pro vyhledávání: '"Hereditary leiomyomatosis and renal cell carcinoma"'
Autor:
Xiaopeng Lan, Mei Feng, Ji Lv, Luchen Zhang, Pengcheng Hu, Yizhen Wang, Yanhui Zhang, Shen Wang, Chunzhao Liu, Chunlei Liu
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
ObjectivesMedical research continues to be extensively devoted to investigating the pathogenesis and treatment approaches of hereditary renal cancer. By aspect including researchers, institutions, countries, journals, and keywords, we conduct a bibli
Externí odkaz:
https://doaj.org/article/d632d34e19a349979b5674689fe8990f
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Hereditary leiomyomatosis and renal cell cancer syndrome is a rare autosomal dominant disease caused by mutations in the fumarate hydratase gene. The syndrome is characterized by skin leiomyomatosis, uterine leiomyomatosis, and renal cell carcinoma.
Externí odkaz:
https://doaj.org/article/f23bb6d513084b54b12b874c78c197a6
Publikováno v:
Clinical Case Reports, Vol 12, Iss 4, Pp n/a-n/a (2024)
Key Clinical Message The patient was found to have multiple uterine myomas at the age of 19, underwent laparoscopic myomectomy at the age of 20, and underwent laparotomic myomectomy again at the age of 23 due to the recurrence of uterine myoma. At th
Externí odkaz:
https://doaj.org/article/bfa69ccfe66c4351a79bd5d537f809f9
Publikováno v:
Xin yixue, Vol 53, Iss 1, Pp 10-13 (2022)
Fumarate hydratase （FH）-deficient uterine leiomyoma is a rare pathological type of uterine leiomyoma, which is caused by FH gene germ-line or system mutations, primarily the latter cause. Although this disease is rare, when it is a sentinel manif
Externí odkaz:
https://doaj.org/article/be39b6f4d4024ebaa565075d08837566
Publikováno v:
Cancer Imaging, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Backgound Fumarate hydratase-deficient renal cell carcinoma (FH-RCC) is a subtype of RCC that is increasingly recognized pathologically. The aim of this study was to evaluate the imaging features of FH-RCC on computed tomography (CT), magnet
Externí odkaz:
https://doaj.org/article/a66fb918e39b407fa3cda560ef2d75ca
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) is a rare genodermatosis characterized by cutaneous leiomyoma (CLM), uterine leiomyoma (ULM) and renal cell carcinoma (RCC). Five HLRCC patients are presented with a compi
Externí odkaz:
https://doaj.org/article/0298ad6359c747c3a916163b3187f695
Autor:
Ziad El-Zaatari, Mukul K Divatia
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 63, Iss 5, Pp 7-17 (2020)
Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) is an autosomal dominant syndrome wherein affected individuals are at risk for the development of cutaneous leiomyomas, early-onset multiple uterine leiomyomas, and an aggressive subtype of r
Externí odkaz:
https://doaj.org/article/8aa8799906e2476683a07076c93be572
Akademický článek
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Akademický článek
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Publikováno v:
BMC Urology, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) is a rare hereditary kidney cancer syndrome in which affected individuals are at risk of skin and uterine leiomyomatosis and kidney cancer. HLRCC-associated kidney cancer
Externí odkaz:
https://doaj.org/article/a159602adf7b417e931c4d31af633224