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Paraneoplastic acrokeratosis

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(Redirected from Acrokeratosis paraneoplastica) This article is about the cutaneous condition Bazex syndrome. For the inherited condition Bazex syndrome, see Bazex–Dupré–Christol syndrome. Medical condition
Paraneoplastic acrokeratosis
Other namesAcrokeratosis paraneoplastica of Bazex and Dupre and acrokeratosis paraneoplastica)
SpecialtyDermatology, oncology

Paraneoplastic acrokeratosis is a skin condition characterized by psoriasiform changes of fingers, toes, ears, and nose, with involvement of the nails and periungual tissues being characteristic and indistinguishable from psoriatic nails. The condition is associated with carcinomas of the upper aerodigestive tract.

History

A case was first reported by Henri Gougerot and C. Grupper in 1922. Andre Bazex described it as a paraneoplastic syndrome in 1965.

See also

References

  1. ^ Fonia, Athina; Baran, Robert (2021). "Cutaneous paraneoplastic syndromes with nail involvement". In Lipner, Shari (ed.). Nail Disorders: Diagnosis and Management, An Issue of Dermatologic Clinics. Elsevier. pp. 175–182. ISBN 978-0-323-70924-8.
  2. James, William D.; Elston, Dirk; Treat, James R.; Rosenbach, Misha A.; Neuhaus, Isaac (2020). "27. Genodermatoses and congenital anomalies". Andrews' Diseases of the Skin: Clinical Dermatology (13th ed.). Edinburgh: Elsevier. pp. 563–565. ISBN 978-0-323-54753-6.
  3. ^ Chiesa-Fuxench, Zelma C.; Ramírez, Liliana; Sánchez, Néstor P. (2011). "Cutaneous manifestations of internal malignancy and paraneoplastic syndromes". In Sánchez, Néstor P. (ed.). Atlas of Dermatology in Internal Medicine. New York: Springer Science & Business Media. p. 66. ISBN 978-1-4614-0687-7.
  4. Gougerot, H. and Grupper, C., (1922). Dermatose érythémato-squameuse avec hyperkératose palmoplantaire, porectasies digitales et cancer de la langue latent. Paris Med, 43, pp.234-237
  5. Bazex, A.; Griffiths, A. (September 1980). "Acrokeratosis paraneoplastica--a new cutaneous marker of malignancy". The British Journal of Dermatology. 103 (3): 301–306. doi:10.1111/j.1365-2133.1980.tb07248.x. ISSN 0007-0963. PMID 7000146.

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ClassificationD
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