Persistent Idiopathic Facial Pain Associated with Somatoform Disorder in an 11-Year-Old Boy

Yoshihiko Sakurai1, Asami Fujii2,3, Fumie Kato2,4

  • 1Department of Pediatrics, Matsubara Tokushukai Hospital, 7-13-26 Amami-higashi, Matsubara, Osaka 580-0032, Japan.

Insights

Persistent idiopathic facial pain (PIFP) in children is rare. This case highlights the potential psychogenic factors and the effectiveness of psychological counseling in managing PIFP symptoms.

Area of Science:

  • Neurology
  • Psychiatry
  • Pediatrics

Background:

  • Persistent idiopathic facial pain (PIFP) is a chronic condition rarely diagnosed in pediatric patients.
  • Facial pain in children can be misdiagnosed, often initially treated for infections like cellulitis.

Observation:

  • An 11-year-old boy presented with recurrent facial pain after a streptococcal infection, initially suspected as trigeminal neuralgia (TN).
  • Diagnostic imaging ruled out vascular compression typical of TN, and the pain's continuous, dull nature differed from TN's sharp, episodic pain.
  • The patient experienced significant functional impairment, including school absence due to malaise, nausea, headache, and anorexia.

Findings:

  • The diagnosis shifted to PIFP after excluding TN and other organic causes.
  • Psychological assessment revealed significant stress related to the patient's social environment.
  • Psychotherapy focusing on stress management led to gradual improvement in the patient's general malaise and facial expression.

Implications:

  • This case underscores the importance of considering psychogenic factors in pediatric PIFP.
  • Psychological counseling and stress management techniques can be valuable therapeutic tools for managing PIFP.
  • Early identification of psychosocial contributors may improve treatment outcomes and functional recovery in children with facial pain.

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