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Intranasal glomus tumor.

A J Potter, G Khatib, S B Peppard

    Archives of Otolaryngology (Chicago, Ill. : 1960)
    |November 1, 1984
    PubMed
    Summary
    This summary is machine-generated.

    Glomus tumors are rare vascular lesions. This case report details the fifth instance of a glomus tumor found in the nasal cavity, highlighting its potential symptoms and curative surgical treatment.

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    Area of Science:

    • Otorhinolaryngology
    • Pathology
    • Surgical Oncology

    Background:

    • Glomus tumors, also known as glomangiomas, are benign neoplasms originating from glomus body cells, typically smooth muscle in origin.
    • These hamartomatous lesions are characterized by vascular channels and epithelioid cells.
    • Glomus tumors are uncommon, particularly in the head and neck region.

    Observation:

    • This report documents the fifth known case of a glomus tumor occurring within the nasal cavity.
    • The observed intranasal glomus tumor was asymptomatic.
    • Previous literature describes symptomatic presentations including nasal obstruction, pain, and epistaxis.

    Findings:

    • Glomus tumors in the nasal cavity are exceptionally rare, with this being the fifth documented case.

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  • The histological composition involves vascular spaces and characteristic epithelioid cells.
  • Complete surgical excision is the standard and curative treatment for glomus tumors.

    • Implications:

    • This case expands the understanding of glomus tumor localization and presentation.
    • Highlights the importance of considering rare diagnoses in the differential for nasal masses.
    • Emphasizes the efficacy of surgical management for intranasal glomus tumors.