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Chondroepitrochlearis Muscle--A Phylogenetic Remnant with Clinical Importance
R-B Tröbs1, B Gharavi2, M Neid3
1Department of Pediatric Surgery, Marienhospital Herne, Ruhr-University of Bochum, Herne, Germany.
Insights
This case report details an infant with an accessory chondroepitrochlearis muscle causing shoulder deformity. Surgical resection of this axillary web normalized function and improved appearance.
Area of Science:
- Anatomy
- Developmental Biology
- Surgical Case Report
Background:
- Accessory muscles, such as the chondroepitrochlearis, are rare anatomical variations.
- These structures can potentially cause clinical symptoms due to their location and attachments.
Observation:
- An infant presented with a cord-like accessory muscle forming an axillary web.
- This anomaly caused restricted movement and abnormal shoulder shape due to humerus tethering.
Findings:
- The accessory muscle, identified as potentially the chondroepitrochlearis, was surgically resected.
- Post-operative follow-up at 7 months showed complete normalization of shoulder function and cosmetic appearance.
Implications:
- This case highlights the importance of recognizing rare accessory muscles in pediatric patients.
- Surgical intervention can effectively correct functional and cosmetic deficits caused by such anomalies.
Abstract:
We report on an infant, presenting with a cord-like accessory muscle crossing the anterior axillary fold. The accessory structure appeared as an axillary web and caused tethering of the humerus together with an abnormal shape of the shoulder. The chondroepitrochlearis muscle is thought to be of phylogenetic origin. In our patient the tendinous sling was resected at the age of 7 month with normalization of function and cosmetics.
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