Difference between revisions of "Hereditary leiomyomatosis and renal cell cancer"
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'''Hereditary leiomyomatosis and renal cell cancer''' is an uncommon syndrome caused by FH (fumarate hydratase) gene mutations.<ref name=omim136850>{{OMIM|136850 | '''Hereditary leiomyomatosis and renal cell cancer''' is an uncommon syndrome caused by FH (fumarate hydratase) gene mutations.<ref name=omim136850>{{OMIM|136850}}</ref> | ||
It is characterized by: | It is characterized by:<ref name=Ref_WMSP290>{{Ref WMSP|290}}</ref> | ||
* [[Papillary renal cell carcinoma]] type 2. | * [[Papillary renal cell carcinoma]] type 2. | ||
* Benign [[leiomyoma]]s skin/[[uterine leiomyoma|uterus]]. | * Benign [[leiomyoma]]s skin/[[uterine leiomyoma|uterus]]. | ||
Revision as of 06:26, 25 July 2014
Hereditary leiomyomatosis and renal cell cancer is an uncommon syndrome caused by FH (fumarate hydratase) gene mutations.[1]
It is characterized by:[2]
- Papillary renal cell carcinoma type 2.
- Benign leiomyomas skin/uterus.
- Uterine leiomyosarcoma.
See also
References
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 136850
- ↑ Humphrey, Peter A; Dehner, Louis P; Pfeifer, John D (2008). The Washington Manual of Surgical Pathology (1st ed.). Lippincott Williams & Wilkins. pp. 290. ISBN 978-0781765275.