ABSTRACT
Platypnea-orthodeoxia is a rare syndrome characterized by dyspnea and deoxygenation induced by a change to a sitting or standing from a recumbent position. It is the result of posturally accentuated intracardiac or pulmonary right-to-left shunt leading to arterial oxygen desaturation. Only few cases of platypnea-orthodeoxia syndrome are reported in the literature and the association between stroke and platypnea-orthodeoxia syndrome with evidence of patent foramen ovale is extremely rare. We describe the case of a 67-year-old female admitted to our Rehabilitation Unit for disabling basilar stroke due to paradoxical embolism from patent foramen ovale that during the first days of rehabilitation showed signs and symptoms of platypnea-orthodeoxia syndrome. To remove a life-threatening condition for the patient and in order to develop the normal rehabilitation project, that was stopped by the platypnea-orthodeoxia syndrome, the patient fastly underwent to percutaneous closure of patent foramen ovale. The stabilization of oxygen arterial saturation with postural changes and the disappearance of symptoms of POS allowed to develop the rehabilitation project with progressive neurological improvement.
Subject(s)
Dyspnea, Paroxysmal/rehabilitation , Foramen Ovale, Patent/complications , Foramen Ovale, Patent/rehabilitation , Stroke Rehabilitation , Vertebrobasilar Insufficiency/etiology , Vertebrobasilar Insufficiency/rehabilitation , Aged , Dyspnea, Paroxysmal/etiology , Female , Foramen Ovale, Patent/surgery , Humans , Hypoxia/etiology , Hypoxia/rehabilitation , Stroke/etiology , Treatment OutcomeABSTRACT
Described are five patients who developed palmaris brevis (PB) spasm syndrome following prolonged use of a computer mouse and keyboard. Electromyography showed spontaneous activity characterized by irregular discharges of single motor unit potentials and myokymia from PB muscle that did not disappear after ulnar nerve block at the wrist, suggesting a distal lesion.
