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Hereditary leiomyomatosis and renal cell carcinoma syndrome: A case report and implications of early onset
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نویسنده
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çaliskan e. ,bodur s. ,ulubay m. ,özmen i. ,çiçek a.f. ,deveci g. ,kaya e.
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منبع
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journal brazilian annals of dermatology - 2017 - دوره : 92 - شماره : 5 - صفحه:88 -91
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چکیده
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Hereditary leiomyomatosis and renal cell carcinoma (hlrcc) is an autosomal dominant manifestation of cutaneous and uterine leiomyomas together with renal cancer due to autosomal dominant germline mutations of fumarate hydratase gene. a twenty-year-old female patient presented with type-ii segmental piloleiomyoma and increased menstruation due to uterine leiomyomas,with a history of bilateral nephrectomy performed at 13 and 16 years of age for type 2 papillary renal cell carcinoma. this case represents one of the very early onsets of hereditary leiomyomatosis and renal cell carcinoma syndrome. as genetic anticipation for renal cancer is a well-documented entity for hlrcc syndrome,early recognition is crucial for both the patient and her family in order to provide appropriate counseling and initiation of surveillance. © 2017 by anais brasileiros de dermatologia.
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کلیدواژه
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Anticipation; Fumarate hydratase; Genetic; Kidney neoplasms; Leiomyomatosis; Mutation
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آدرس
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department of dermatology,gulhane school of medicine,ankara, Turkey, department of obstetrics and gynecology,gulhane school of medicine,ankara, Turkey, department of obstetrics and gynecology,gulhane school of medicine,ankara, Turkey, department of dermatology,çorlu state hospital,tekirdag, Turkey, department of pathology,gulhane school of medicine,ankara, Turkey, department of pathology,gulhane school of medicine,ankara, Turkey, department of urology,gulhane school of medicine,ankara, Turkey
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Authors
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