Optometry and vision science : official publication of the American Academy of Optometry · 2014
Delayed recurrence of intracranial chordoma.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
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.
Alldredge Brooks R, Meers George W
Аннотация
PURPOSE: Although a chordoma is extremely rare, it commonly presents with ocular symptoms, often impacting one or more cranial nerves.
CASE REPORT: The authors describe a unique case of rapidly developing intracranial chordoma that recurred 9 years after the original mass was successfully diagnosed and treated. It is noteworthy that, although the tumor originated within the cranium at the base of the skull, it presented primarily with clinical signs of a unilateral orbital mass because of tumor extension.
CONCLUSIONS: The lifetime recurrence rate for chordoma is high after treatment; therefore, a high level of suspicion is warranted in any patient with new symptoms and a history of intracranial chordoma.
CASE REPORT: The authors describe a unique case of rapidly developing intracranial chordoma that recurred 9 years after the original mass was successfully diagnosed and treated. It is noteworthy that, although the tumor originated within the cranium at the base of the skull, it presented primarily with clinical signs of a unilateral orbital mass because of tumor extension.
CONCLUSIONS: The lifetime recurrence rate for chordoma is high after treatment; therefore, a high level of suspicion is warranted in any patient with new symptoms and a history of intracranial chordoma.