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Anaplastic Hemangiopericytoma of the Jugular Foramen: Case Report and Systematic Review

Journal

WORLD NEUROSURGERY
Volume 153, Issue -, Pages 11-20

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.wneu.2021.06.094

Keywords

Anaplastic hemangiopericytoma; Jugular foramen tumor; Solitary fibrous tumor

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This study presented a rare case of anaplastic HPC in the jugular foramen and conducted a systematic review of the literature concerning JF HPC/SFTs. It highlights the importance of tissue diagnosis and appropriate management in such cases.
BACKGROUND: Hemangiopericytomas (HPCs) and solitary fibrous tumors (SFTs) are rare tumors of mesenchymal origin. Here, the authors present a rare case of anaplastic HPC in the jugular foramen (JF). The authors also conduct a systematic review of the literature to examine the current fund of knowledge on JF HPC/SFTs. METHODS: A systematic MEDLINE search was conducted using key words hemangiopericytoma OR solitary fibrous tumor AND jugular foramen OR extracranial OR skull base. Clinicopathologic characteristics and outcomes of the present case were reviewed and compared with those in the literature. RESULTS: A 41-year-old male, who had undergone stereotactic radiation therapy 6 years ago for a presumed glomus jugulare tumor, presented to our institution with worsening dysphagia, hoarseness, persistent tongue weakness, and radiographic evidence of tumor progression. The patient underwent uncomplicated gross total resection with sacrifice of the infiltrated hypoglossal nerve. Histopathologic evaluation revealed anaplastic HPC/SFT (World Health Organization grade III). Review of the literature yielded 9 additional cases of JF HPC/SFT in 5 males (56%) and 4 females (44%), with a mean age of 49.6 years old. Patients commonly presented with pain (37.5%) and lower cranial nerve deficits (100%). Preoperative diagnoses included glomus jugulare (n = 2) or JF schwannomas (n = 3). All patients underwent microsurgical resection of the lesion, except for 1 who refused all treatment after diagnostic biopsy. CONCLUSION: The authors present the only reported case of anaplastic HPC of the JF. The illustrative case and those found on systematic review of the literature highlight the importance of tissue diagnosis and appropriate management.

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