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特发性肺纤维化患者局部通气-灌注不匹配的原因:一项CT与闪烁扫描联合研究

Cause of regional ventilation-perfusion mismatching in patients with idiopathic pulmonary fibrosis: a combined CT and scintigraphic study.

作者信息

Strickland N H, Hughes J M, Hart D A, Myers M J, Lavender J P

机构信息

Department of Diagnostic Radiology, Royal Postgraduate Medical School, Hammersmith Hospital, London, United Kingdom.

出版信息

AJR Am J Roentgenol. 1993 Oct;161(4):719-25. doi: 10.2214/ajr.161.4.8372745.

Abstract

OBJECTIVE

Regional ventilation and perfusion were studied in patients with idiopathic pulmonary fibrosis (cryptogenic fibrosing alveolitis) to seek an explanation for the mismatched ventilation/perfusion (V/Q) seen on scintigrams, which may suggest pulmonary embolic disease.

SUBJECTS AND METHODS

Eight patients with idiopathic pulmonary fibrosis were examined with inspiratory and expiratory CT scans. Planar and tomographic (single-photon emission computed tomography, SPECT) scintigraphy, using inhalation of krypton-81m gas (ventilation) and IV injection of 99mTc-albumin macroaggregates (perfusion), also was performed. The lungs were divided into quadrants (cranial, caudal, right, left) for analysis.

RESULTS

Cystic air spaces with a "honeycomb" appearance occupied more than 33% of the cross-sectional area in 75% of all lung quadrants (n = 16), more than 66% of the area in 44% of quadrants, and less than 33% of the area in the remaining 25% of quadrants. On expiratory CT scans, the cross-sectional area of the cystic spaces diminished significantly (unlike emphysematous spaces). Sixty-seven percent of lung quadrants, corresponding to those with marked or moderate involvement with cystic spaces, showed a mismatched V/Q pattern on scintigrams (absent perfusion, normal ventilation); 27% of quadrants had matched V/Q defects, and 6% did not show defects. Two patients had, in addition, large cystic spaces typical of emphysema, but the coexistent fibrosis prevented the gross air trapping seen in bullous emphysema.

CONCLUSION

The cystic air spaces that are often seen on CT scans of patients with idiopathic pulmonary fibrosis are unperfused (probably due to vascular obliteration) but are usually normally ventilated. This V/Q mismatch on scintigrams explains the large physiologic dead space seen at rest and on exercise and could suggest pulmonary embolism unless a CT scan is obtained. Conversely, the larger cystic spaces might be mistaken for emphysema unless V/Q scintigraphy is done.

摘要

目的

研究特发性肺纤维化(隐源性纤维性肺泡炎)患者的局部通气与灌注情况,以解释在闪烁扫描图上所见的通气/灌注(V/Q)不匹配现象,这种不匹配可能提示肺栓塞疾病。

对象与方法

对8例特发性肺纤维化患者进行吸气和呼气CT扫描检查。还采用吸入81m氪气(通气)和静脉注射99m锝 - 白蛋白大聚合体(灌注)进行平面和断层(单光子发射计算机断层扫描,SPECT)闪烁扫描。将肺分为象限(头侧、尾侧、右侧、左侧)进行分析。

结果

呈“蜂窝”状外观的囊状气腔在所有肺象限的75%(n = 16)中占横截面积的33%以上,在44%的象限中占面积的66%以上,在其余25%的象限中占面积不到33%。在呼气CT扫描中,囊状气腔的横截面积显著减小(与肺气肿气腔不同)。67%的肺象限,对应于那些有明显或中度囊状气腔累及的象限,在闪烁扫描图上显示V/Q不匹配模式(灌注缺失,通气正常);27%的象限有匹配的V/Q缺陷,6%未显示缺陷。另外两名患者有典型的肺气肿大囊状气腔,但并存的纤维化阻止了大疱性肺气肿中所见的明显气体潴留。

结论

特发性肺纤维化患者CT扫描中常见的囊状气腔未灌注(可能由于血管闭塞),但通常通气正常。闪烁扫描图上的这种V/Q不匹配解释了静息和运动时所见的较大生理死腔,并且可能提示肺栓塞,除非进行CT扫描。相反,除非进行V/Q闪烁扫描,较大的囊状气腔可能会被误诊为肺气肿。

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