Barwell, "
Cowden's syndrome with immunodeficiency," Journal of Medical Genetics, vol.
Cowden syndrome is a serious genetic disorder characterized by multiple hemartomas usually of skin, but also of thyroid, G.I tract, Bones, CNS, Eyes and G.U tract
Cowden's syndrome is considered part of PTEN hemartomas tumor syndrome (PHTS) which also includes Bannyan--Riley --Ruvalcaba syndrome, proteus syndrome, and proteus--like syndrome.
The dermatopathology of
Cowden's syndrome. Br J Dermatol.
In patients with
Cowden's syndrome, retroperitoneal fibrosis, mediastinal fibrosis, sclerosing cholangitis, Riedel's thyroiditis, and inflammatory pseudotumor of the orbit can all manifest, either alone or in combination.
Cowden's syndrome (Multiple Hamartoma Syndrome): This rare condition is characterized by the presence of gastro intestinal, oral and cutaneous hamartomas and neoplasms of the breast and thyroid.
Cowden's syndrome is considered part of PTEN hemartomas tumor syndrome (PHTS) which also includes Bannyan--Riley --Ruval caba syndrome, proteus syndrome, and proteus--like syndrome.