Bazex syndrome (acrokeratosis paraneoplastica) diagnosed in a patient with oral persistent ulcerations

Head Neck Pathol. 2010 Dec;4(4):312-7. doi: 10.1007/s12105-010-0203-5. Epub 2010 Aug 19.

Abstract

Paraneoplastic syndromes associated with head and neck cancer are rare and have been reported under dermatological, endocrine, hematological, neurological and rheumatological disorders. Bazex syndrome is an intriguing paraneoplasia that can be associated with head and neck squamous cell carcinomas. A range of symmetrical dermatological manifestations, with a clear predilection to extremities, that encompasses erythematous squamous plaques, skin scaling and nail dystrophy can provide a psoriasiform pattern in Bazex syndrome. In addition to these tricky clinical features, the rarity of the disease and the lack of understanding on Bazex syndrome generally make such cases to be mismanaged as psoriasis or lichen planus, causing an important delay in the diagnosis of the underlying malignancy. The authors describe a case of Bazex syndrome that occurred in a patient with a recently diagnosed tongue squamous cell carcinoma. Clinicians should consider paraneoplasia when assessing skin and/or oral persistent lesions.

Publication types

  • Case Reports

MeSH terms

  • Aneurysm / pathology
  • Carcinoma, Basal Cell / pathology
  • Fatal Outcome
  • Histiocytoma, Benign Fibrous / pathology
  • Humans
  • Hypotrichosis / pathology
  • Male
  • Middle Aged
  • Mucous Membrane / pathology
  • Onycholysis / pathology*
  • Oral Ulcer / pathology*
  • Paraneoplastic Syndromes / pathology*
  • Penile Diseases / pathology
  • Skin / pathology
  • Skin Diseases, Papulosquamous / pathology*
  • Skin Neoplasms / pathology

Supplementary concepts

  • Bazex-Dupre-Christol syndrome