Shafiq Maria, Ali Natasha
Department of Pathology and Microbiology, Aga Khan University and Hospital, Karachi, Pakistan.
Am J Case Rep. 2013 Oct 16;14:416-8. doi: 10.12659/AJCR.884020. eCollection 2013.
Male, 20 FINAL DIAGNOSIS: Sickle cell anemia Symptoms: Bone marrow necrosis • bone pain • fever • hepatomegaly • icterus • splenomegaly • weakness
Unusual clinical course.
In sickle cell disease, bone involvement is the commonest clinical presentation in the acute as well as chronic setting presenting as painful vaso-occlusive crisis and avascular necrosis, respectively. Other complications include bone marrow necrosis and infarction.
We report a case of a 20-year-old male who was referred for bone marrow evaluation due to symptoms of fever, weakness, and repeated episodes of bone pains. Bone trephine biopsy revealed multiple areas of central necrosis surrounded by fibroblasts.
Recognition of necrosis through bone trephine biopsy is important for early initiation of therapy.
男性,20岁 最终诊断:镰状细胞贫血 症状:骨髓坏死、骨痛、发热、肝肿大、黄疸、脾肿大、虚弱
不寻常的临床病程
在镰状细胞病中,骨骼受累是急性和慢性情况下最常见的临床表现,分别表现为疼痛性血管闭塞危象和无血管性坏死。其他并发症包括骨髓坏死和梗死。
我们报告一例20岁男性,因发热、虚弱和反复骨痛症状被转诊进行骨髓评估。骨穿刺活检显示多个中央坏死区域被成纤维细胞包围。
通过骨穿刺活检识别坏死对于早期开始治疗很重要。