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A cavernous sinus cavernous hemangioma. Case report.

B Rosenblum, A S Rothman, C Lanzieri

    Journal of Neurosurgery
    |November 1, 1986
    PubMed
    Summary
    This summary is machine-generated.

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    This case study highlights a rare intracavernous hemangioma in a patient with Turner

    Area of Science:

    • Endocrinology
    • Neurosurgery
    • Genetics

    Background:

    • Turner's syndrome is a genetic condition associated with various health issues.
    • Intracavernous hemangiomas are rare vascular tumors.
    • Estrogen's role in hemangioma pathogenesis is an area of ongoing research.

    Observation:

    • A patient diagnosed with Turner syndrome presented with symptoms attributed to an intracavernous hemangioma.
    • Clinical presentation included neurological signs and symptoms consistent with a space-occupying lesion in the cavernous sinus.
    • Radiological imaging confirmed the presence and extent of the hemangioma.

    Findings:

    • The study highlights the extreme rarity of co-occurring Turner syndrome and intracavernous hemangioma.
    • Surgical excision of the hemangioma was successfully performed, resulting in no postoperative neurological deficits.

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  • Evidence suggests a potential role for estrogens in the pathogenesis of this specific hemangioma in the context of Turner syndrome.

    • Implications:

    • This case underscores the importance of considering rare diagnoses in patients with genetic syndromes.
    • The successful surgical outcome suggests that complete resection is a viable treatment option for intracavernous hemangiomas.
    • Further investigation into the hormonal influences, particularly estrogens, on vascular tumor formation is warranted.