Vasconcelos Alexandra, Prior Ana Rita, Ferrão Anabela, Morais Anabela
Paediatrics Department, Hospital Professor Doutor Fernando Fonseca, Lisboa, Portugal.
BMJ Case Rep. 2012 Apr 28;2012:bcr1120115146. doi: 10.1136/bcr.11.2011.5146.
Sickle-cell anaemia (SCA) is a multi-system disease, associated with episodes of acute illness and progressive organ damage. Disease severity shows substantial variation and it is often a burden for adolescents. Complications such as leg ulcer and priapism have a significant impact on quality of life. There are still no definitive treatment guidelines available. Considering the embarrassing nature of priapism and the dire consequences for erectile dysfunction, it is important to inform patients, parents and providers about the relationship of SCA to prolonged painful erections. This article will review the pathophysiology and treatment options of SCA focusing the complications of leg ulcers, priapism, cholelithiasis and retinopathy. The case study of a 14-year-old boy is used to present a management challenge of multiple SCA-related complications.
镰状细胞贫血(SCA)是一种多系统疾病,与急性发病和进行性器官损害相关。疾病严重程度差异很大,对青少年来说往往是一种负担。腿部溃疡和阴茎异常勃起等并发症对生活质量有重大影响。目前仍没有明确的治疗指南。考虑到阴茎异常勃起的尴尬性质以及勃起功能障碍的严重后果,告知患者、家长和医护人员SCA与长期疼痛性勃起之间的关系很重要。本文将回顾SCA的病理生理学和治疗选择,重点关注腿部溃疡、阴茎异常勃起、胆石症和视网膜病变等并发症。通过一个14岁男孩的案例研究来呈现与多种SCA相关并发症的管理挑战。