Levey D S, MacCormack L M, Sartoris D J, Haghighi P, Resnick D, Thorne R
Department of Radiology, Spohn Health Systems, Corpus Christi, TX 78404, USA.
Skeletal Radiol. 1996 Apr;25(3):287-93. doi: 10.1007/s002560050082.
The objective of this article was to offer a better characterization of the typical clinical presentation, radiologic findings, histology, treatment approaches, and differential diagnosis of cystic angiomatosis, a rare condition of which previous reports have been confusing because of unclear diagnostic criteria, different classifications, and variations in terminology. A case report using the improved imaging techniques of computed tomography scanning is presented in addition to an analysis and review of the previous literature, which relied heavily on plain film radiography, biopsy, and necropsy for diagnosis. A case report of a 26-year-old man initially symptomatic at age 12 is presented. Although a rare condition, cystic angiomatosis must be considered in pediatric and young adult patients presenting with diffuse, multifocal, cystic skeletal lesions, with or without visceral involvement.
本文的目的是更好地描述囊性血管瘤病的典型临床表现、放射学表现、组织学、治疗方法及鉴别诊断。囊性血管瘤病是一种罕见疾病，由于诊断标准不明确、分类不同及术语存在差异，以往的报告令人困惑。除了对以往主要依靠平片、活检及尸检进行诊断的文献进行分析和综述外，还呈现了一份使用计算机断层扫描这种改进成像技术的病例报告。报告了一名26岁男性的病例，其在12岁时首次出现症状。尽管囊性血管瘤病较为罕见，但对于出现弥漫性、多灶性囊性骨骼病变（无论有无内脏受累）的儿童及青年成人患者，必须考虑到该病。
