Flaherty K R, Travis W D, Colby T V, Toews G B, Kazerooni E A, Gross B H, Jain A, Strawderman R L, Flint A, Lynch J P, Martinez F J
Department of Radiology, University of Michigan Health System, University of Michigan School of Public Health, Ann Arbor, Michigan 48109-0360, USA.
Am J Respir Crit Care Med. 2001 Nov 1;164(9):1722-7. doi: 10.1164/ajrccm.164.9.2103074.
Findings of surgical lung biopsy (SLB) are important in categorizing patients with idiopathic interstitial pneumonia (IIP). We investigated whether histologic variability would be evident in SLB specimens from multiple lobes in patients with IIP. SLBs from 168 patients, 109 of whom had multiple lobes biopsied, were reviewed by three pathologists. A diagnosis was assigned to each lobe. A different diagnosis was found between lobes in 26% of the patients. Patients with usual interstitial pneumonia (UIP) in all lobes were categorized as concordant for UIP (n = 51) and those with UIP in at least one lobe were categorized as discordant for UIP (n = 28). Patients with nonspecific interstitial pneumonia (NSIP) in all lobes were categorized as having fibrotic (n = 25) or cellular NSIP (n = 5). No consistent distribution of lobar histology was noted. Patients concordant for UIP were older (63 +/- 9 [mean +/- SD] yr; p < 0.05 as compared with all other groups) than those discordant for UIP (57 +/- 12 yr) or with fibrotic NSIP (56 +/- 11 yr) or cellular NSIP (50 +/- 9 yr). Semiquantitative high-resolution computed tomography demonstrated a varied profusion of fibrosis (p < 0.05 for all group comparisons), with more fibrosis in concordant UIP (2.13 +/- 0.62) than in discordant UIP (1.42 +/- 0.73), fibrotic NSIP (0.83 +/- 0.58), or cellular NSIP (0.44 +/- 0.42). Survival was better for patients with NSIP than for those in both UIP groups (p < 0.001), although survival in the two UIP groups was comparable (p = 0.16). Lobar histologic variability is frequent in patients with IIP, patients with a histologic pattern of UIP in any lobe should be classified as having UIP.
外科肺活检(SLB)的结果对于特发性间质性肺炎(IIP)患者的分类很重要。我们研究了IIP患者多个肺叶的SLB标本中组织学变异性是否明显。三位病理学家对168例患者的SLB进行了回顾,其中109例患者进行了多个肺叶的活检。为每个肺叶做出诊断。26%的患者不同肺叶之间存在不同诊断。所有肺叶均为普通型间质性肺炎(UIP)的患者被归类为UIP一致(n = 51),至少一个肺叶为UIP的患者被归类为UIP不一致(n = 28)。所有肺叶均为非特异性间质性肺炎(NSIP)的患者被归类为纤维化型(n = 25)或细胞型NSIP(n = 5)。未观察到肺叶组织学的一致分布。UIP一致的患者比UIP不一致的患者(57±12岁)、纤维化型NSIP患者(56±11岁)或细胞型NSIP患者(50±9岁)年龄更大(63±9 [平均±标准差]岁;与所有其他组相比,p < 0.05)。半定量高分辨率计算机断层扫描显示纤维化程度各不相同(所有组间比较p < 0.),UIP一致组的纤维化程度(2.13±0.62)高于UIP不一致组(1.42±0.73)、纤维化型NSIP组(0.83±0.58)或细胞型NSIP组(0.44±0.42)。NSIP患者的生存率优于两个UIP组的患者(p < 0.001),尽管两个UIP组的生存率相当(p = 0.16)。IIP患者中肺叶组织学变异性很常见,任何肺叶具有UIP组织学模式的患者都应归类为患有UIP。