Dincer H Erhan, Raza Tasleem
Veteran Affairs Southern Nevada Health Care System, Pulmonary and Critical Care Medicine, Las Vegas, NV, USA.
WMJ. 2005 Aug;104(6):67-71.
Sickle cell trait is a relatively common condition in the African-American population. Individuals with this condition may have any of several complications under rare circumstances. We report a patient who presented with extensive compartment syndrome leading to death. A 31-year-old African-American male with known history of sickle cell trait developed extensive compartment syndrome followed by rhabdomyolysis, severe acidosis, acute renal failure, and coagulopathy. Although the patient underwent multiple fasciotomies for extensive compartment syndrome and received aggressive resuscitation with massive transfusions of blood, blood products and intravenous fluids, he died. Multiple compartment syndromes in patients with sickle cell trait represent a very unusual complication and can cause significant morbidity and mortality. Avoidance of strenuous exercise, especially in hot climates, early diagnosis, and aggressive therapy are very important to prevent this catastrophic complication.
镰状细胞性状在非裔美国人中是一种相对常见的情况。患有这种情况的个体在极少数情况下可能会出现几种并发症中的任何一种。我们报告了一名出现广泛骨筋膜室综合征并导致死亡的患者。一名有镰状细胞性状已知病史的31岁非裔美国男性发生了广泛的骨筋膜室综合征,随后出现横纹肌溶解、严重酸中毒、急性肾衰竭和凝血病。尽管该患者因广泛的骨筋膜室综合征接受了多次筋膜切开术,并接受了大量输血、血液制品和静脉输液的积极复苏治疗,但他还是死亡了。镰状细胞性状患者出现多处骨筋膜室综合征是一种非常罕见的并发症,可导致显著的发病率和死亡率。避免剧烈运动,尤其是在炎热气候下,早期诊断和积极治疗对于预防这种灾难性并发症非常重要。