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Familial leiomyomatosis cutis affecting nine family members in two successive generations including four cases of Reed's syndrome.
Indian J Dermatol Venereol Leprol ; 2013 Jan-Feb; 79(1): 83-87
Article in English | IMSEAR | ID: sea-147398
ABSTRACT
Reed's syndrome or familial leiomyomatosis cutis et uteri is an autosomal dominant disorder, characterized by multiple cutaneous and uterine leiomyomas. We report here a case of a 53-year-old woman who presented to us with multiple painful nodules over different parts of her body. Based on the histopathological examination, imaging, and past medical records, a diagnosis of Reed's syndrome was made. Three of her sisters had similar disease. Subsequently, it was found that a total of nine members of their family in two successive generations were affected with cutaneous leiomyomas. The present case series has been reported for its interesting clinical presentations and rarity.
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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pedigree / Skin Neoplasms / Uterine Neoplasms / Female / Humans / Leiomyomatosis / Genetic Predisposition to Disease / Fumarate Hydratase / Middle Aged Language: English Journal: Indian J Dermatol Venereol Leprol Year: 2013 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pedigree / Skin Neoplasms / Uterine Neoplasms / Female / Humans / Leiomyomatosis / Genetic Predisposition to Disease / Fumarate Hydratase / Middle Aged Language: English Journal: Indian J Dermatol Venereol Leprol Year: 2013 Type: Article