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Priapism and sickle-cell anemia: diagnosis and nonsurgical therapy.

机译:精神分裂症和镰状细胞性贫血:诊断和非手术治疗。

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INTRODUCTION: Priapism describes a persistent erection lasting longer than 4 hours. Ischemic priapism and stuttering priapism are phenotypic manifestations of sickle-cell disease (SCD). AIMS: To define the types of priapism associated with SCD, to address pathogenesis, and to recommend best practices. SOURCES: Literature review and published clinical guidelines. SUMMARY OF FINDINGS: Priapism is a full or partial erection that persists more than 4 hours. There are three kinds of priapism: ischemic priapism (veno-occlusive, low flow), stuttering priapism (recurrent ischemic priapism), and nonischemic priapism (arterial, high flow). Ischemic priapism is a pathologic phenotype of SCD. Ischemic priapism is a urologic emergency when untreated priapism results in corporal fibrosis and erectile dysfunction. The recommended treatment for ischemic priapism is decompression of the penis by needle aspiration and if needed, injection (or irrigation) with dilute sympathomimetic drugs. Stuttering priapism describes a pattern of recurring unwanted painful erections in men with SCD. Patients typically awaken with an erection that persists for several hours and becomes painful. The goals of managing stuttering ischemic priapism are: prevention of future episodes, preservation of erectile function, and balancing the risks vs. benefits of various treatment options. The current molecular hypothesis for stuttering priapism in SCD proposes that insufficient basal levels of phosphodiesterase type-5 are available in the corpora to degrade cyclic guanosine monophosphate (cGMP). Nocturnal erections result from normal neuronal production and surges of cGMP. In the context of SCD stuttering priapism, these nocturnal surges in cGMP go unchecked, resulting in stuttering priapism. CONCLUSIONS: Considering the embarrassing nature of the problem and the dire consequences to erectile function, it is important to inform patients, parents, and providers about the relationship of SCD to prolonged painful erections. Prompt diagnosis and appropriate medical management of priapism are necessary to spare patients surgical interventions and preserve erectile function.
机译:简介:精神分裂症描述持续性勃起持续超过4个小时。缺血性快感和口吃性快感是镰状细胞病(SCD)的表型表现。目的:定义与SCD相关的阴茎异常勃勃的类型,解决发病机理,并推荐最佳实践。资料来源:文献复习和出版的临床指南。结果总结:精神分裂症是完全或部分勃起,持续超过4个小时。阴茎异常勃起症(静脉闭塞,低血流),口吃性阴茎异常勃起(反复性缺血性阴茎异常)和非缺血性阴茎异常(动脉,高血流)有三种。缺血性阴茎异常勃起是SCD的病理表型。当未经治疗的阴茎异常勃起导致体质纤维化和勃起功能障碍时,缺血性阴茎异常勃起是泌尿外科急症。缺血性阴茎异常勃起的推荐治疗方法是通过针吸术对阴茎减压,必要时用稀释的拟交感神经药注射(或冲洗)。口吃的狂妄症描述了SCD男性复发性不想要的痛苦勃起的模式。患者通常会勃起,这种勃起会持续数小时并变得疼痛。控制口吃性缺血性精神病的目标是:预防未来发作,保留勃起功能以及平衡各种治疗方案的风险与收益。当前关于SCD口吃性快感的分子假设提出,语料库中没有足够的基础水平的5型磷酸二酯酶来降解环鸟苷单磷酸(cGMP)。夜间勃起是由正常的神经元产生和cGMP激增引起的。在SCD口吃狂妄者的背景下,cGMP的这些夜间发作无节制,导致口吃狂妄者。结论:考虑到问题的尴尬性质和对勃起功能的严重后果,重要的是告知患者,父母和提供者SCD与长时间痛苦的勃起的关系。及时诊断和对阴茎异常勃勃的病人进行适当的医疗管理对于使患者免受手术干预和保持勃起功能是必要的。

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