Lee K S, Kullnig P, Hartman T E, Müller N L
Department of Radiology, University of British Columbia, Vancouver, Canada.
AJR Am J Roentgenol. 1994 Mar;162(3):543-6. doi: 10.2214/ajr.162.3.8109493.
Description of the CT findings of cryptogenic organizing pneumonia has been limited to a small number of cases. This study was performed to characterize the CT findings of this disease in a larger number of cases and to compare the findings in immunocompetent and immunocompromised patients.
The CT scans of 43 (32 immunocompetent and 11 immunocompromised) patients who had biopsy-proved cryptogenic organizing pneumonia were reviewed. The scans were obtained by using contiguous 8- or 10-mm collimation and selected thin (1.5 or 2.0 mm) section (n = 23), thin-section collimation at 10-mm intervals (n = 12), or 8- or 10-mm collimation only (n = 8). The scans were analyzed by three observers, and final decisions were reached by consensus.
The most common pattern seen was consolidation, which was present alone or as part of a mixed pattern in 34 cases (79%). The consolidation had a predominantly subpleural and/or peribronchovascular distribution in 27 cases (63%). Ground-glass attenuation and nodules were seen in 26 patients (60%) and 13 patients (30%), respectively, and were usually random in distribution. Consolidation was present in 91% (29/32) of immunocompetent and 45% (5/11) of immunocompromised patients (p < .01). Ground-glass attenuation was present in 56% (18/32) of immunocompetent and 73% (8/11) of immunocompromised patients (p > .25). Nodules were present in seven (22%) of 32 immunocompetent patients and six (55%) of 11 immunocompromised patients (p < .025).
We conclude that in immunocompetent patients the CT findings in cryptogenic organizing pneumonia most commonly consist of bilateral areas of consolidation involving mainly the subpleural and/or peribronchovascular regions. In the immunocompromised patient, the CT findings are variable.
关于隐源性机化性肺炎的CT表现描述仅限于少数病例。本研究旨在对更多病例的该疾病CT表现进行特征描述,并比较免疫功能正常和免疫功能低下患者的表现。
回顾了43例经活检证实为隐源性机化性肺炎患者的CT扫描结果(32例免疫功能正常,11例免疫功能低下)。扫描采用8或10mm连续准直,并选取薄层(1.5或2.0mm)扫描(n = 23)、10mm间隔的薄层准直扫描(n = 12)或仅采用8或10mm准直扫描(n = 8)。由三名观察者对扫描结果进行分析,并通过共识达成最终诊断。
最常见的表现为实变,34例(79%)单独出现或作为混合表现的一部分。27例(63%)实变主要分布于胸膜下和/或支气管血管周围。分别有26例(60%)和13例(30%)患者出现磨玻璃影和结节,且通常呈随机分布。免疫功能正常患者中91%(29/32)出现实变,免疫功能低下患者中45%(5/11)出现实变(p <.01)。免疫功能正常患者中56%(18/32)出现磨玻璃影,免疫功能低下患者中73%(8/11)出现磨玻璃影(p >.25)。32例免疫功能正常患者中有7例(22%)出现结节,11例免疫功能低下患者中有6例(55%)出现结节(p <.025)。
我们得出结论,免疫功能正常患者隐源性机化性肺炎的CT表现最常见的是双侧实变区域,主要累及胸膜下和/或支气管血管周围区域。免疫功能低下患者的CT表现则各不相同。