Leiomyomatosis associated with Reed syndrome: Case report
Introduction Reed syndrome, or Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC), is a rare autosomal dominant disorder first described by Reed et al. in 1973 [1]. It is characterized by the presence of cutaneous piloleiomyomas and uterine leiomyomas in women, with a genetic basis linked to mutations in the fumarate hydratase (FH) gene located on […]