Leiomiomatosis cutánea y uterina múltiple o síndrome de Reed: estudio retrospectivo de 13 casos
Author:
Publisher
Elsevier BV
Subject
Dermatology,Histology,Pathology and Forensic Medicine
Reference26 articles.
1. Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology;Kiuru;Am J Pathol,2001
2. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer;Tomlinson;Nat Genet,2002
3. Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43;Alam;Am J Hum Genet,2001
4. Piloleiomiomas faciales múltiples no familiares;Pastor;Actas Dermosifiliogr,2001
5. Familial leiomyomatosis: A review and discussion of pathogenesis;Garman;Dermatology,2003
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1. Atypical manifestations of uterine leiomyomas – expecting the unexpected;Case Reports in Women's Health;2023-12
2. Dermatologists might be the first to suspect hereditary leiomyomatosis and renal cell carcinoma syndrome;Anais Brasileiros de Dermatologia;2023-09
3. Reed’s syndrome: a combination of a renal cyst with leiomyoma of the skin and uterus (clinical observation);Russian Journal of Skin and Venereal Diseases;2022-08-23
4. Solitary painful nodule on the scapular region;Actas Dermo-Sifiliográficas;2022-02
5. Solitary painful nodule on the scapular region;Actas Dermo-Sifiliográficas (English Edition);2021-11
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