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A Case of Reed's Syndrome(Familial Leiomyomatosis Cutis Et Uteri) / 대한피부과학회지
Korean Journal of Dermatology ; : 612-616, 2007.
Article in Korean | WPRIM | ID: wpr-183509
ABSTRACT
Reed's syndrome is a rare, autosomal dominant disease with incomplete penetrance that is characterized by uterine and cutaneous leiomyomas. We report a case of Reed's syndrome in a 50-year-old woman. The patient underwent removal of the uterine leiomyoma at the age of 36. Following this the patient noticed development of multiple, cutaneous nodules on both arms at the age of 45. These nodules progressively increased in both number and size, while appearing in other sites. The histopathologic finding of an isolated, single skin lesion showed typical leiomyoma arising from arrector pilorum muscle. Familial history revealed that her father had been affected with similar cutaneous lesions.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Arm / Skin / Leiomyomatosis / Penetrance / Fathers / Leiomyoma Limits: Female / Humans Language: Korean Journal: Korean Journal of Dermatology Year: 2007 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Arm / Skin / Leiomyomatosis / Penetrance / Fathers / Leiomyoma Limits: Female / Humans Language: Korean Journal: Korean Journal of Dermatology Year: 2007 Type: Article