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Isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review. | LitMetric

AI Article Synopsis

  • Temporalis muscle hypertrophy is a rare condition, especially when it occurs unilaterally, with only 9 cases documented in English literature since 1990, and this report features the youngest known case, a 7-year-old girl.
  • The patient presented with a painless swelling in the right temporalis muscle, lacking signs of inflammation, trauma, or other abnormalities, and was diagnosed through imaging and muscle biopsy showing normal structure.
  • The case emphasizes the need for careful diagnosis, even in rare pediatric conditions, as it can help rule out other potential health issues.

Article Abstract

Background: Temporalis muscle hypertrophy is a rare entity of masticatory muscle hypertrophy. All types of masticatory muscle hypertrophies have been documented of which temporalis muscle hypertrophy is one. Temporalis muscle hypertrophy is most commonly bilateral and usually associated with other types of masticatory muscles hypertrophy such as masseter or pterygoid hypertrophy. However, isolated unilateral temporalis muscle hypertrophy is extremely rare and only 9 cases have been reported to date in English literature since 1990 with only two patients less than 18 years. There is no exact etiology identified and the diagnosis is made by muscle biopsy combined with imaging study to exclude other possibilities. Age at presentation is ranges from 15 to 65 years with involvement of both sexes. We report the youngest child who is a seven year old girl with right side isolated unilateral temporalis muscle hypertrophy.

Case Presentation: In this patient, we discuss the youngest child with isolated unilateral temporalis muscle hypertrophy and literature review to date. The patient is a seven year old female presenting with painless swelling of the right temporalis muscle. There had no features of inflammation, trauma, neoplasm or history of parafunctions such as bruxism. The child was not complaining significantly headache or visual disturbances as well. She had undergone radiological assessment with ultrasound scan and contrast MRI. The diagnosis was confirmed by muscle biopsy which shows normal muscle architecture. She was managed conservatively with regular follow up.

Conclusion: Isolated unilateral temporalis muscle hypertrophy is extremely rare in children. However this case raises the importance of considering alternative diagnoses despite the condition being rare in the pediatric population.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817789PMC
http://dx.doi.org/10.1186/s12887-018-1061-7DOI Listing

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