TY - JOUR KW - Female KW - Fumarate Hydratase KW - Genetic Predisposition to Disease KW - Humans KW - Leiomyomatosis KW - Middle Aged KW - Neoplastic Syndromes, Hereditary KW - Pedigree KW - Skin Neoplasms KW - Uterine Neoplasms AU - Mandal RK AU - Koley S AU - Banerjee S AU - Kabiraj SP AU - Ghosh SK AU - Kumar P AB -
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.
BT - Indian journal of dermatology, venereology and leprology C1 - http://www.ncbi.nlm.nih.gov/pubmed/23254734?dopt=Abstract DA - 2013 Jan-Feb DO - 10.4103/0378-6323.104674 IS - 1 J2 - Indian J Dermatol Venereol Leprol LA - eng N2 -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.
PY - 2013 SP - 83 EP - 7 T2 - Indian journal of dermatology, venereology and leprology TI - Familial leiomyomatosis cutis affecting nine family members in two successive generations including four cases of Reed's syndrome. VL - 79 SN - 0973-3922 ER -