Sequential treatments in Hereditary Leiomyomatosis and Renal Cell Carcinoma (HLRCC). Case report and review of the literature.
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چکیده
منابع مشابه
Hereditary leiomyomatosis and renal cell carcinoma (HLRCC syndrome): a case report
Recently multiple cutaneous leiomyomas, uterine leiomyoimatosis and renal cancer have been described as a cancer syndrome with autosomal dominant pattern of inheritance.We report a 79-year-old man who presented with multiple hyperkertotic erythematous nodules on his right leg with histological diagnosis of pilar leiomyoma. In his past medical history several systemic co...
متن کاملHereditary leiomyomatosis and renal cell carcinoma
Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) is an autosomal-dominant hereditary syndrome, which is caused by germline mutations in the FH gene that encodes the tricarboxylic acid cycle enzyme fumarate hydratase (FH). HLRCC patients are predisposed to develop cutaneous leiomyomas, multiple, symptomatic uterine fibroids in young women resulting in early hysterectomies, and early on...
متن کاملA Case of Hereditary Leiomyomatosis and Renal Cell Carcinoma
A 49-year-old lady presented with multiple recurring painful lesions over her thighs, arms, and back. Past medical history included a left sided nephrectomy for renal cell carcinoma and a hysterectomy for multiple uterine fibroids (leiomyomas). Histopathological examination revealed changes consistent with pilar leiomyomas. Gene mutation analysis confirmed a diagnosis of hereditary leiomyomatos...
متن کاملRenal Capillary Hemangioma Mimicking Urothelial Carcinoma, A Case Report and Review of the Literature
Renal hemangioma is a rare tumor which can be capillary or cavernous. There have been less than 30 renal capillary hemangioma cases reported in the English literature. Herein we will report a case of renal hemangioma which was detected in a 74-year-old man operated with the impression of urothelial carcinoma of hilum.
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ژورنال
عنوان ژورنال: Canadian Urological Association Journal
سال: 2015
ISSN: 1920-1214,1911-6470
DOI: 10.5489/cuaj.2264