Desselle B C, O'Brien T, Bugnitz M, Beaty O, Wilimas J, Helton K
Department of Pediatrics, LeBonheur Children's Medical Center, University of Tennessee College of Medicine, Memphis 38103, USA.
Pediatr Hematol Oncol. 1995 Mar-Apr;12(2):159-62. doi: 10.3109/08880019509029549.
We describe a case of an adolescent with sickle-beta+ thalassemia who developed fatal fat embolism syndrome. After presenting with bone pain, the patient developed mental status changes, hypoxemia, and died following cardiorespiratory arrest.
我们描述了一例患有镰状β+地中海贫血的青少年发生致命性脂肪栓塞综合征的病例。在出现骨痛后，患者出现精神状态改变、低氧血症，并在心肺骤停后死亡。
