Duplicate Omohyoid Muscle Causing Progressive Dysphagia and Dyspnea: A Case Report.

Introduction: Duplicate omohyoid muscles are uncommon anomalies and exceedingly rare causes of progressive clinical symptoms. The goals of this case report are to describe the clinical characteristics, cross-sectional imaging, intraoperative findings, and curative treatment of our patient, to develop a differential diagnosis for this condition, and to review the pertinent literature regarding this particular type of anomalous omohyoid muscle as one among many variations.
Case Presentation: A 20 year-old man presented with progressive limited neck range of motion followed by dysphagia and then dyspnea caused by his duplicate omohyoid muscle. He underwent curative surgery in 2015 at our tertiary care center.
Discussion: Although rare, a duplicate omohyoid muscle should be considered in the differential diagnosis of dysphagia and dyspnea with concurrent central neck deformity. We report the first case, to our knowledge, of an anomalous omohyoid that caused significant progressive clinical symptoms. Direct excision of the restrictive anomalous tissue proved curative.