Familial dermal eccrine cylindromatosis with emphasis on histology and genetic mapping
نویسندگان
چکیده
منابع مشابه
Familial Dermal Eccrine Cylindromatosis with Emphasis on Histology and Genetic Mapping
Familial cylindromatosis (FC) is an autosomal dominant disorder with apparently complete penetrance, but variable expression. There is an increasing evidence that FC is clinically, genetically, and histologically heterogeneous disorder as the simultaneous occurrence of cylindromas and other tumors of skin appendages within the affected individuals and families. The presence of multiple scalp cy...
متن کاملPorokeratotic eccrine ostial and dermal duct nevus with extensive linear distribution: a case report
Porokeratotic eccrine ostial and dermal duct nevus (PEODDN) is known as an uncommon disorder of keratinization in which acrosyringium is involved; however, its causes have yet remained unknown. It is presented clinically by discrete keratotic papules on distal extremities arranged in a linear pattern along Blaschko lines. Histopathologically, it is characterized by cornoid lamella, which is alm...
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چکیده ندارد.
15 صفحه اولPorokeratotic eccrine ostial and dermal duct nevus with sensory polyneuropathy and hyperthyroidism: Report of a case
The case, who discribed here is a 66-year-old man with one year history of asymptomatic, keratotic papules with a linear distribution on the skin of his right palm near the wrist. On histopathological examination cornoid lamella-like parakeratotic columns above eccrine sweat ducts were observed. The acrosyringium was also dilated. He had been followed up for predominantly sensory polyneur...
متن کاملPorokeratotic Eccrine Ostial and Dermal Duct Nevus
Comedo-like lesions of the palm, present since birth, are studied electronmicroscopically and their eccrine nature demonstrated. We suggest their inclusion under the name porokeratotic eccrine-ostial and dermal duct nevus previously proposed by Abell and Read.
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ژورنال
عنوان ژورنال: Annals of Medical and Health Sciences Research
سال: 2013
ISSN: 2141-9248
DOI: 10.4103/2141-9248.121207