An uncommon first manifestation of multiple sclerosis: Tako-Tsubo cardiomyopathy. (May 2016)

• Record Type: Journal Article
• Authors: Midaglia, Luciana; Juega Mariño, Jesús M; Sastre-Garriga, Jaume; Rovira, Alex; Vidal-Jordana, Angela; López-Pérez, María A; Marzo-Sola, María E; Librada Escribano, Fausto; Montalban, Xavier
• Is Part Of: Multiple sclerosis. Volume 22:Number 6(2016)
• Page Start: 842
• Page End: 846
• Publication Date: 2016-05
• Subjects: Tako-Tsubo cardiomyopathy -- multiple sclerosis -- solitary tract nucleus -- autonomic nervous system -- clinically isolated syndrome; Central nervous system -- Diseases -- Periodicals; Myelin sheath -- Diseases -- Periodicals; Inflammation -- Periodicals; Multiple sclerosis -- Periodicals; Central Nervous System Diseases -- Periodicals; Demyelinating Diseases -- Periodicals; Inflammation -- Periodicals; Multiple Sclerosis -- Periodicals; Système nerveux central -- Maladies -- Périodiques; Gaine de myéline -- Maladies -- Périodiques; Inflammation (Pathologie) -- Périodiques; Sclérose en plaques -- Périodiques; Electronic journals; 616.834005
• DOI: 10.1177/1352458516638557
• Languages: English
• ISSNs: 1352-4585

Abstract

Background: Clinically isolated syndromes affecting the brainstem may present with rare manifestations such as neurogenic pulmonary oedema (NPO). Objectives: We present the case of a 23 year-old man with NPO caused by Tako-Tsubo cardiomyopathy (TTC) as a first manifestation of multiple sclerosis (MS). Methods and Results: A brain magnetic resonance imaging scan at admission showed multiple supra and infratentorial white matter inflammatory demyelinating lesions. This examination was repeated 2 and 4 weeks after symptoms onset and active lesions showing contrast uptake were identified, two of them involving the pons and the medulla oblongata, probably affecting the solitary tract nucleus. Cerebrospinal fluid oligoclonal bands were detected. The patient was treated with a 3-day course of 1g intravenous methylprednisolone presenting a significant and progressive improvement. The proposed underlying physiopathology is an excessive secretion of catecholamines resulting in myocardial stunning and ventricular failure. Two months later he developed optic neuritis and disease-modifying treatment was initiated. Conclusions: Clinicians should consider a possible neurological origin of TTC, and according to the clinical characteristics of the patient, MS may be suspected.