Shah R M, Friedman A C
Department of Radiologic Sciences, Medical College of Pennsylvania, Philadelphia 19129, USA.
AJR Am J Roentgenol. 1998 Mar;170(3):719-21. doi: 10.2214/ajr.170.3.9490960.
The CT angiogram sign--that is, the ability to see normal pulmonary vasculature within parenchymal consolidations--was initially reported as specific for the diagnosis of bronchioloalveolar cell carcinoma. Our purpose was to establish the frequency of this sign in lobar consolidations of varied causes as revealed by contrast-enhanced CT. We also sought to determine if the presence of this sign contributed to the specificity of radiographic diagnosis.
All consecutive contrast-enhanced thoracic CT examinations performed for evaluation of lobar consolidations between May 1994 and April 1997 were reviewed. The CT angiogram sign was considered present when segments of pulmonary vessels could be identified within alveolar consolidations. Medical records were reviewed to establish the causes of the consolidations.
Fifty-one patients (24 women, mean age = 59 years; 27 men, mean age = 46 years) had lobar or multilobar consolidations due to pneumonia without central obstruction (n = 20), pneumonia or pneumonitis with central obstruction (n = 19), passive atelectasis (n = 7), and (one case each) mucus plugging, lipoid pneumonia, pulmonary lymphoma, bronchioloalveolar cell carcinoma, and pulmonary hemorrhage. The CT angiogram sign was present in 15 (29%) of 51 consolidations, including seven (37%) of 19 postobstructive consolidations, four (20%) of 20 cases of pneumonia without central obstruction, one (14%) of seven cases of passive atelectasis, and each single case of lymphoma, bronchioloalveolar cell carcinoma, and lipoid pneumonia.
The CT angiogram sign is a common finding in lobar consolidations evaluated by contrast-enhanced CT. However, the sign does not add specificity to the radiographic diagnosis.
CT血管造影征,即实质实变区内可见正常肺血管的能力,最初被报道为细支气管肺泡癌诊断的特异性表现。我们的目的是通过增强CT确定该征象在各种病因导致的肺叶实变中的出现频率。我们还试图确定该征象的存在是否有助于影像学诊断的特异性。
回顾了1994年5月至1997年4月期间为评估肺叶实变而进行的所有连续胸部增强CT检查。当肺泡实变区内可识别出肺血管段时,认为存在CT血管造影征。查阅病历以确定实变的病因。
51例患者(24例女性,平均年龄59岁;27例男性,平均年龄46岁)出现肺叶或多肺叶实变,病因包括无中央阻塞的肺炎(n = 20)、有中央阻塞的肺炎或肺炎性病变(n = 19)、被动性肺不张(n = 7),以及各1例的黏液嵌塞、类脂性肺炎、肺淋巴瘤、细支气管肺泡癌和肺出血。51例实变中有15例(29%)出现CT血管造影征,包括19例阻塞后实变中的7例(37%)、20例无中央阻塞肺炎中的4例(20%)、7例被动性肺不张中的1例(14%),以及淋巴瘤、细支气管肺泡癌和类脂性肺炎各1例。
CT血管造影征是增强CT评估肺叶实变时的常见表现。然而,该征象并未增加影像学诊断的特异性。