A 31-year-old man presented to the hospital after suffering a sudden cardiac arrest. Despite optimal therapy, the patient passed away. His medical history included febrile rash at age 2. At autopsy, there was aneurysmal dilation and severe coronary artery stenosis by atherosclerotic plaques and myocardial fibrosis. These findings were presumed to be due to complications of Kawasaki disease, given the remote history of severe febrile rash as a toddler and the presence of chronic coronary artery injury, recanalization, and thrombosis with ischemic heart disease leading to sudden cardiac collapse and death.
Introducción. La ataxia espinocerebelosa es un grupo de desórdenes genéticos que consisten en una degeneración progresiva que afecta principalmente al cerebelo, el tronco encefálico y la médula espinal, y se asocia de forma variable con otros síntomas neurológicos. Presentación del caso. Mujer de 60 años sin antecedentes médicos relevantes, quien consultó al servicio de fisiatría por cuadro clínico de dos años de evolución consistente en alteración progresiva en la marcha, pérdida de fuerza en miembros inferiores, temblor en miembros superiores, disfagia y fatiga. Al examen físico se encontró disartria leve, disdiadococinesia, dismetría, sacadas hipométricas bilaterales y marcha atáxica. Se realizó resonancia magnética nuclear (RMN) del cerebro que mostró atrofia cerebelosa, y electromiografía y neuroconducciones que confirmó polirradiculoneuropatía axonal. Las pruebas genéticas moleculares evidenciaron expansión de una de una repetición de pentanucleotidos ATTCT, lo que confirmó el diagnóstico de ataxia cerebelosa tipo 10 (SCA10). Se inició manejo multidisciplinario donde fisiatría inició plan de rehabilitación neurológica, manejo del dolor con neuromodulador y prescripción de dispositivo de asistencia para la movilidad tipo caminador. La paciente mejoró su independencia en actividades de la vida diaria: el índice de Barthel pasó de 45 puntos a 75 tras 12 semanas en rehabilitación neurológica. Conclusión. La SCA10 se consideró inicialmente como una ataxia cerebelosa pura asociada a convulsiones; sin embargo, en los últimos años la identificación de nuevas familias con este desorden ha revelado fenotipos más diversos, incluyendo polineuropatía, signos piramidales y deterioro cognitivo y neuropsiquiátrico. Se describe aquí un caso de SCA10 de inicio tardío (más de 50 años de edad) que podría ser el primero esporádico reportado en Colombia.
Introduction: Albuquerque New Mexico is the "hot air balloon capital of the world," with balloons flying throughout the year and during the Albuquerque International Balloon Fiesta. The medical literature regarding morbidity and mortality in hot air balloon accidents is relatively scarce.Methods: A series of fatal, hot air balloon accidents were identified by querying and analyzing the databases of the Office of the Medical Investigator in New Mexico from 1972 to 2021.Results: Twenty-one lethal cases from 11 hot air balloon accidents were evaluated. Fifty-seven percent of decedents were male, the age range was 29 to 74 years, and all the decedents were White. Causes of death were certified as multiple injuries (52.4%), blunt trauma (42.9%), and electrocution (4.76%). The manner of death was accidental in all cases. Most common autopsy findings were rib fractures (100%), pelvic fractures (81.8%), and subarachnoid hemorrhage (72.7%). October was the month with the most accidents (63.63%), the most common cause was the pilot's failure to maintain clearance from obstacles (14.3%), and the most frequent collision was with power lines (63.6%).Conclusions: Hot air balloon fatalities are rare, and the patterns of injury resemble those seen in free falls from significant heights with extensive blunt trauma.
Introduction: Myofascial pain syndrome is an acute and chronic painful musculoskeletal condition that involves muscle and surrounding connective tissue. Trigger point injection is a common treatment for this condition providing long-term relief. The procedure is generally safe; however some side effects have been reported including pain, nerve injury, bleeding, infection, and pneumothorax. Objective: To report a case of a patient with myofascial pain syndrome successfully treated by Ultra Sound-guided infiltration of a myofascial trigger point in the rhomboid major muscle. Case description: A 39-year-old presented with cervical and dorsal pain of 4 months of evolution. She had physical and occupational therapy, with partial improvement of cervical pain but persistence of dorsal pain. No abnormal finding was noted on the neurological examination. On palpation, the patient had a myofascial trigger point in the left rhomboid major muscle. Given the persistence of the myofascial trigger point after physical therapy, it was considered the patient might benefit from Ultra Sound-guided infiltration. No adverse events were reported. At the end of the procedure, the patient reported a 70% reduction in pain. The patient returned for a follow-up visit one month after the procedure, reporting pain relief of 80%. Conclusions: The use of an Ultra Sound-guided technique for trigger point injection decreases the risk of iatrogenic complications. The blind method may result in poor localization of the point. Further studies are required to develop Ultra Sound based criteria to determine its clinical use.
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