Congenital striated muscle hamartoma of the temporalis muscle: an index presentation

Striated muscle hamartomas are rare, benign malformations of disorganised but mature striated muscle fibres. This case report presents a congenital striated muscle hamartoma (CSMH) in a primary school-going girl, involving the temporalis and frontalis muscles-an unprecedented and atypical location. The patient exhibited a progressively enlarging swelling in the left temporal region, initially suspected to be a capillary haemangioma or rhabdomyoma based on imaging findings. However, a definitive diagnosis was achieved through histopathological evaluation, which confirmed CSMH. Complete surgical excision ensured excellent long-term outcomes with no recurrence over six years of follow-up. The report highlights the limited literature outcomes on CSMHs in atypical locations and underscores the importance of histopathological confirmation for accurate diagnosis and management.

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Publication Details

Journal
BMJ Case Reports
Published
2026-02-01
DOI
https://doi.org/10.1136/bcr-2025-267135
Primary Topic
Tumors and Oncological Cases
Type
article
Field-Weighted Citation Impact
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article

Congenital striated muscle hamartoma of the temporalis muscle: an index presentation

Dipika Choudhary, Shilpi Karmakar
BMJ Case Reports
Tumors and Oncological Cases
article

Congenital striated muscle hamartoma of the temporalis muscle: an index presentation

Dipika Choudhary, Shilpi Karmakar
article en

Abstract

Striated muscle hamartomas are rare, benign malformations of disorganised but mature striated muscle fibres. This case report presents a congenital striated muscle hamartoma (CSMH) in a primary school-going girl, involving the temporalis and frontalis muscles-an unprecedented and atypical location. The patient exhibited a progressively enlarging swelling in the left temporal region, initially suspected to be a capillary haemangioma or rhabdomyoma based on imaging findings. However, a definitive diagnosis was achieved through histopathological evaluation, which confirmed CSMH. Complete surgical excision ensured excellent long-term outcomes with no recurrence over six years of follow-up. The report highlights the limited literature outcomes on CSMHs in atypical locations and underscores the importance of histopathological confirmation for accurate diagnosis and management.

BMJ Case ReportsVol. 19(2)
All India Institute of Medical Sciences Jodhpur (IN), King George's Medical University (IN)
Openalex Percentile: Top 59%
Tumors and Oncological Cases
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