A Presentation of Meige Syndrome With Associated Upper Motor Neuron Symptoms

• Published in: Curēus (Palo Alto, CA) CA), 2024-05, Vol.16 (5), p.e60101
• Main Authors: Valencia Uribe, Jeffrey, Hossain, Nazia, Rizvi, Hassnain, Qureshi, Mohammed
• Format: Article
• Language: English
• Subjects: Anatomy; Botulinum toxin; Dysarthria; Dysphagia; Dystonia; Electromyography; Fractures; Magnetic resonance imaging; Medical imaging; Movement disorders; Neuroimaging; Neurology; Patients; Therapeutics; Tremor (Muscular contraction)
• ISSN: 2168-8184; 2168-8184
• DOI: 10.7759/cureus.60101

Meige syndrome (MS) is a cranial dystonia that involves blepharospasm and oromandibular dystonia. It can also evolve to include other adjacent muscle groups in the cervical region. It typically presents in middle-aged females, and while the disorder is relatively uncommon, its exact prevalence varies. Diagnosis is typically made with a thorough history and physical and workup to rule out other causes. Treatment options include medical management with gamma-aminobutyric acid (GABA) antagonists, dopamine antagonists, and anticholinergics for short-term management. Long-term treatment options are Botox and deep brain stimulation. This case report presents a 56-year-old female with a complex presentation of MS; the patient's symptoms progressed from isolated blepharospasms to involve orofacial and cervical musculature. A distinctive aspect of this case was the simultaneous presence of upper motor neuron (UMN) signs in the patient alongside acute to subacute compression fractures of the superior endplate of C7 and T3, as revealed by cervical spine imaging. Treatment with clonazepam led to significant symptomatic improvement, highlighting the importance of a multimodal approach in managing MS. This case underscores the need for careful clinical evaluation, collaboration with movement disorder specialists, and ongoing research efforts to enhance understanding and treatment of MS.