Related Experiment Video

Updated: Nov 1, 2025

Adapting Human Videofluoroscopic Swallow Study Methods to Detect and Characterize Dysphagia in Murine Disease Models
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Intermittent dysphagia revealing a lateropharyngeal neurofibroma in a child: Case report: A case report

Wydadi Omar1, Ahmed Brahim Ahmedou1, Oukessou Youssef1

  • 1ENT, Head and Neck Surgery Department, Ibn Rochd UniversityHospital, Faculty of Medicine and Pharmacy, Hassan II, Casablanca, Morocco.

Annals of Medicine and Surgery (2012)
|June 25, 2021
PubMed

Insights

Neurofibromatosis type 1 (NF1) can present with cervical neurofibromas causing dysphagia. Conservative management with regular monitoring may be appropriate for slow-growing tumors in NF1 patients.

Area of Science:

  • Medical Genetics
  • Pediatric Neurology

Background:

  • Neurofibromatosis type 1 (NF1) is a genetic disorder.
  • Characterized by café-au-lait spots, neurofibromas, and potential neoplasms.

Observation:

  • A 12-year-old patient with NF1 presented with dysphagia and a cervical neurofibroma.
  • Symptoms included intermittent dysphagia and a sensation of food attachment.

Findings:

  • The patient was monitored for two years with annual CT scans.
  • Minimal progression of dysphagia and no significant growth of the cervical mass were observed.

Implications:

  • Treatment for NF1-related cervical neurofibromas is not standardized.
  • Conservative management and watchful waiting can be a viable approach.
Abstract

Keywords:
Abstention therapeuticChildDysphaiaNeck regionType 1 neurofibromatosis

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