Squamous cell carcinoma of the hypopharynx

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Squamous cell carcinoma of the hypopharynx

ORPHA:494547Disease

What it is

A rare head and neck tumor characterized by a malignant epithelial neoplasm with evidence of squamous differentiation, most commonly located in the piriform sinus, less frequently the posterior pharyngeal wall or the postcricoid area. The tumor can spread directly to adjacent structures or metastasize via lymphatic and blood vessels to regional lymph nodes, or lung, liver, and bones, respectively. Primary risk factors are tobacco smoking and (to a lesser extent) alcohol consumption. Patients may present with odynophagia, dysphagia, signs and symptoms related to a neck mass, voice changes, otalgia, and constitutional symptoms.

Key facts

Prevalence
1-9 / 100 000 (annual incidence, Europe)
Age of onset
Adult, Elderly
Inheritance
Not applicable
Classified as
Disease

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Genes

ING1Disease-causing somatic mutation(s)
PTENDisease-causing somatic mutation(s)
TNFRSF10BMajor susceptibility factor

ICD-10 codes

C12ICD-10 uses a narrower term
C13.0ICD-10 uses a narrower term
C13.2ICD-10 uses a narrower term
C13.8ICD-10 uses a narrower term

Cross-references

MEDDRA 10041849MONDO 0044638OMIM 275355UMLS C0280321

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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