Multiple cutaneous leiomyoma
Multiple cutaneous leiomyoma | |
---|---|
Other names: Hereditary leiomyomatosis and renal cell cancer [1] | |
a)Multiple cutaneous leiomyomas initial presentation b) 1 month after initial lesions were treated/carbon dioxide laser ablation c) 6 months postoperative | |
Specialty | Dermatology |
Multiple cutaneous leiomyomas, also known as Pilar leiomyomas,[2] arise from the arrectores pilorum muscles, and are made up of a poorly circumscribed proliferation of haphazardly arranged smooth muscle fibers located in the dermis that appear to infiltrate the surrounding tissue and may extend into the subcutis.[2]
Sometimes associated with uterine leiomyomas (a combination known as multiple cutaneous and uterine leiomyomatosis, MCUL), these lesions may also be a manifestation of the hereditary leiomyomatosis and renal cell cancer syndrome.
See also
References
- ↑ "Hereditary leiomyomatosis and renal cell cancer | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 28 April 2019. Retrieved 28 April 2019.
- 1 2 Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). Page 1033. McGraw-Hill. ISBN 0-07-138076-0.
External links
Classification | |
---|---|
External resources |
|
This article is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.