Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Feb 19;18(1):71.
doi: 10.1186/s12887-018-1061-7.

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

Affiliations
Review

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

Jagath C Ranasinghe et al. BMC Pediatr. .

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.

Keywords: IUTMH in pediatrics; Isolated unilateral temporalis muscle hypertrophy; Sri Lanka.

PubMed Disclaimer

Conflict of interest statement

Authors’ information

JCR (MBBS, DCH) is a trainee MD pediatrics affiliated with the Teaching Hospital Kandy Sri Lanka. CW (MBBS,DCH,MD,FCCP) is a consultant pediatrician at the Teaching Hospital Kandy Sri Lanka. GR (MBBS, MD) is a consultant radiologist at the Teaching Hospital Kandy Sri Lanka.

Ethics approval and consent to participate

Not applicable

Consent for publication

Written informed consent was obtained from the parents of the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor-In-Chief of this journal.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
Isolated right temporalis muscle hypertrophy on an axial MRI image. T2W image of the cMRI study demonstrating enlarged right temporalis muscle on an axial section without abnormal contrast enhancement. White arrow head indicate enlarged right temporalis muscle
Fig. 2
Fig. 2
Isolated right temporalis muscle hypertrophy on a coronal MRI image. T2W image of the cMRI study demonstrating enlarged right temporalis muscle on a coronal section without abnormal contrast enhancement. White arrow head indicate enlarged right temporalis muscle

References

    1. Legg JW. Enlargement of the temporal and masseter muscles on both sides. Trans Pathol Soc L. 1880;31:361–366.
    1. Kessel LJ. Benign bilateral masseteric hypertrophy with temporal muscle involvement. Oral Surgery, Oral Med. Oral Pathol. [Internet]. 1970 [cited 2016 Feb 5];30:450–3. Available from: https://www.sciencedirect.com/science/article/pii/0030422070901568 - PubMed
    1. Kalish GH. Hypertrophy of the Masseter or Temporalis Muscles or Both. Arch. Pediatr. Adolesc. Med. [Internet]. American Medical Association; 1971 [cited 2016 Feb 4];121:346. Available from: https://jamanetwork.com/journals/jamapediatrics/article-abstract/503983?... - PubMed
    1. Da Silva K, Mandel L. Bilateral temporalis muscle hypertrophy: a case report. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. [Internet]. 2006 [cited 2015 Sep 16];102:e1–3. Available from: http://www.oooojournal.net/article/S1079-2104(06)00077-1/fulltext - PubMed
    1. Kim HJ, Yum KW, Lee SS, Heo MS, Seo K. Effects of botulinum toxin type a on bilateral masseteric hypertrophy evaluated with computed tomographic measurement. Dermatologic Surg. 2003;29:484–489. - PubMed

LinkOut - more resources