BMJ case reports · 2021
Diverse manifestations of a sickle cell crisis.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Hashemzehi Tumaj, Bertok Szabolcs, Figaszewska Malwina Julia, Batura Deepak
Аннотация
We describe the case of a 21-year-old man with a background of sickle cell disease (SCD) who was on acute presentation in a sickle cell crisis required immediate intensive care admission with red blood cell exchange and ventilatory support. He had right frontal lobe infarcts and extensive bilateral deep white matter lesions most likely secondary to fat embolism. Inpatient investigations demonstrated a patent foramen ovale, explaining the route of spread of the fat embolus. He then had a transcatheter closure of the atrial defect. The patient needed prolonged inpatient rehabilitation. He was discharged from hospital in a wheelchair secondary to severe lower limb neurology and bilateral knee heterotopic ossification. He lives with the possibility of early onset dementia and cognitive decline, requiring constant care. The case highlights the multiple manifestations of SCD and their diverse and debilitating consequences.
Предметные рубрики MeSH
Anemia, Sickle CellBrain InfarctionCognitive DysfunctionContractureEchocardiographyEmbolism, FatErythrocyte TransfusionForamen Ovale, PatentFrontal LobeHumansIntensive Care UnitsKnee JointLeukoencephalopathiesMagnetic Resonance ImagingMaleNeuralgiaOssification, HeterotopicPlasmaPlatelet TransfusionPolyneuropathiesQuadriplegiaYoung Adult