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What is acrokeratosis neoplastica? Acrokeratosis neoplastica is a rare skin condition with features rather like psoriasis. It is associated with squamous cell carcinoma of the upper respiratory or gastrointestinal tract. Acrokeratosis neoplastica is far more common in males than in females.
Bazex-Dupré-Christol syndrome is a rare genodermatosis characterised by the triad of congenital hypotrichosis and follicular atrophoderma, with subsequent development of multiple basal cell carcinomas. It is categorised as an ' ectodermal dysplasia with an hereditary tumour' syndrome.
Bazex–Dupré–Christol syndrome is a very rare condition inherited in an X-linked dominant fashion. Physical findings typically include follicular atrophoderma, multiple basal cell carcinomas, hypotrichosis, and hypohidrosis. [2] Genetics. BCDS is inherited in an X-linked dominant manner.
22 maj 2023 · Bazex syndrome, also known as acrokeratosis paraneoplastica or acrokeratosis neoplastica (AN) syndrome is a rare, acral psoriasiform dermatosis associated with internal malignancies, most frequently squamous cell carcinoma of the upper aerodigestive tract.
Paraneoplastic acrokeratosis, or Bazex syndrome is a cutaneous condition characterized by psoriasiform changes of hands, feet, ears, and nose, with involvement of the nails and periungual tissues being characteristic and indistinguishable from psoriatic nails.
Acrokeratosis paraneoplastica or Bazex syndrome is a rare, obligate paraneoplastic skin manifestation, typically characterized by rapid appearance of acral exfoliative, psoriasiform lesions, and palmoplantar keratosis [1].
10 lut 2007 · The association of acral hyperkeratosis and malignancy was first described by Bazex in 1965. 1 Bazex syndrome generally affects men over the age of 40 years and has universally been associated with malignancy in over 125 case reports.
