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Purpose: To subclassify parapharyngeal extension in nasopharyngeal carcinoma (NPC) and investigate its prognostic value and staging categories based on magnetic resonance imaging (MRI).
Methods And Materials: Data from 1504 consecutive NPC patients treated with definitive-intent radiotherapy were analyzed retrospectively. Sites of parapharyngeal extension were defined by MRI. Overall survival (OS), local relapse-free survival (LRFS), and distant metastasis-free survival (DMFS) were calculated by the Kaplan-Meier method and compared with the log-rank test. Hazard consistency and hazard discrimination were determined by multivariate analysis with Cox proportional hazards models.
Results: 1104 patients (73.4%) had parapharyngeal extension; 1.7-63.8% had involvement of various anatomic sites. The hazard ratio for death was significantly higher with extensive parapharyngeal extension (lateral pterygoid muscle of masticator space and beyond or parotid space) than with mild extension (medial pterygoid muscle of masticator space, or carotid, prestyloid, and prevertebral or retropharyngeal space). OS, LRFS, and DMFS with extensive parapharyngeal extension were similar to those in T4 disease; OS, LRFS, and DMFS with mild parapharyngeal extension were significantly higher than in those T3 disease (all P ≤ 0.015).
Conclusions: Parapharyngeal extension in NPC should be subclassified as mild or extensive, which should be regarded as stages T2 and T4 diseases, respectively.
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http://dx.doi.org/10.1155/2015/749515 | DOI Listing |
Cureus
August 2025
Pathology, Hanoi Medical University, Hanoi, VNM.
Parapharyngeal space (PPS) tumors are extremely rare in the pediatric population, accounting for a small fraction of all head and neck neoplasms. The majority of neoplasms in the PPS are benign tumors. We present a case of an eight-year-old male with a large PPS ganglioneuroma, who presented with a neck mass that had been progressing over five years with no symptoms of dysphasia.
View Article and Find Full Text PDFCase Rep Otolaryngol
August 2025
Department of Surgery, The Aga Khan University, Karachi 74800, Pakistan.
Schwannomas are benign, slow-growing tumors that develop from Schwann cells in the nerve sheath and can occur in peripheral, cranial, or autonomic nerves. Foramen ovale schwannomas are a rare variant in the head and neck region representing 1%-2% of all intracranial schwannomas, with parapharyngeal space involvement complicating surgical resection. A 48-year-old male presented with headaches after an episode of light-headedness along with facial pain.
View Article and Find Full Text PDFSage Open Pediatr
May 2025
Ibn Sina University Hospital Center, Rabat, Morocco.
Cerebellopontine meningiomas in pediatric patients are exceptionally rare, with cases involving extracranial extension being even less common. These tumors present significant surgical challenges due to their complex anatomical location and potential for extensive involvement of surrounding structures. Imaging is crucial in evaluating the extent of the tumor, assessing cranial nerve involvement, excluding other differential diagnoses, and facilitating optimal treatment planning.
View Article and Find Full Text PDFIndian J Otolaryngol Head Neck Surg
July 2025
Department of Radiology, Smita Memorial Hospital and Research Centre, Thodupuzha, Kerala India.
Congenital thymic cysts are rare benign neck masses found primarily in the paediatric population, comprising only 0.3% of congenital neck cysts in children. These cysts arise from embryonal thymic tissue along its descent path, with mediastinal extension seen in approximately 50% of cases.
View Article and Find Full Text PDFDiscov Oncol
May 2025
Department of Cancer Center, Army Medical Center of PLA, Army Medical University, No. 10 Changjiang Zhilu, Yuzhong District, Chongqing, 400042, China.
Introduction: Solitary fibrous tumor (SFT) of the central nervous system (CNS) is a spindle cell neoplasm originating from mesenchymal tissue. SFT is prone to local recurrence or distant metastasis. The main sites of metastasis include the liver, lung, and bone.
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