Hypopharyngeal cancer pathophysiology

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Faizan Sheraz, M.D. [2]

Overview

Genes involved in the pathogenesis of hypopharyngeal cancer include p16, NOTCH1, and cyclin D1. Hypopharyngeal cancer is associated with sideropaenic dysphagia and Paterson Brown Kelly syndrome.On gross pathology, flattened plaques, mucosal ulceration, and raised margins of the lesion are characteristic findings of hypopharyngeal cancer. On microscopic histopathological analysis, spindle cells, basaloid cells, and nuclear atypia are characteristic findings of hypopharyngeal cancer.[1]

Pathophysiology

Genetics

Genes involved in the pathogenesis of hypopharyngeal cancer include:

  • p16
  • NOTCH1
  • cyclin D1
  • TP53

Associated Diseases

Hypopharyngeal carcinoma is associated with:[1]

  • Sideropaenic dysphagia
  • Paterson Brown Kelly syndrome

Gross Pathology

Gross pathology of hypopharyngeal cancer includes:[1]

  • Flattened plaques
  • Raised margins of the lesion
  • Mucosal ulceration
  • Tumor spread to piriform sinus

Microscopic Pathology

Microscopic features of hypopharyngeal carcinoma include:[1]

References

  1. 1.0 1.1 1.2 1.3 Helliwell TR (2003). "acp Best Practice No 169. Evidence based pathology: squamous carcinoma of the hypopharynx". J Clin Pathol. 56 (2): 81–5. PMC 1769882. PMID 12560383.

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