Department of Surgical Pathology, Toho University School of Medicine, 6-11-1, Omori-Nishi, Ota-Ku, Tokyo, 143-8541, Japan.
Diagn Pathol. 2011 Mar 30;6:27. doi: 10.1186/1746-1596-6-27.
Pulmonary tumor thrombotic microangiopathy (PTTM) has been known as a rare and serious cancer-related pulmonary complication. However, the pathogenesis and pathophysiology of this debilitating condition still remains obscure and no effective management was recommended. The present study aims to elucidate the pathophysiology of PTTM.
Autopsy records were searched to extract cases of pulmonary tumor embolism induced by metastasis of gastric carcinoma in the Toho University Omori Medical Center from 2000 to 2006. And then, tissue sections of extracted cases were prepared for not only light microscopic observation but morphometric analysis with the use of selected PTTM cases.
Six autopsies involved PTTM and clinicopathological data of them were summarized. There was a significant negative association between pulmonary arterial diameter and stenosis rate in four cases. Although all cases showed an increase of stenosis rate to some degree, the degree of stenosis rate varied from case to case. Significant differences were found for average stenosis rate between the under 100 micrometer group or the 100 to 300 micrometer group and the 300 micrometer group in four cases. However, no significant differences were found for average stenosis rate between the under 100 micrometer group and the 100 to 300 micrometer group in all cases. Meanwhile, all cases showed positive reactivity for tissue factor (TF), five showed positive reactivity for vascular endothelial growth factor (VEGF), and three showed positive reactivity for osteopontin (OPN).
In the present study, we revealed that the degree of luminal narrowing of the pulmonary arteries varied from case to case, and our results suggested that pulmonary hypertension in PTTM occurs in selected cases which have a widespread pulmonary lesion with severe luminal narrowing in the smaller arteries. Furthermore, our immunohistochemical examination indicated that gastric carcinoma indicating PTTM shows a higher TF-positive rate than typical gastric carcinoma. However, it remains still obscuring whether gastric carcinoma indicating PTTM shows a higher VEGF or OPN-positive rate as determined by immunohistochemistry.
肺肿瘤血栓性微血管病(PTTM)已被认为是一种罕见且严重的与癌症相关的肺部并发症。然而,这种使人虚弱的疾病的发病机制和病理生理学仍然不清楚,也没有推荐有效的治疗方法。本研究旨在阐明 PTTM 的病理生理学。
在 2000 年至 2006 年期间,我们在东京都立大学大森医疗中心的尸检记录中搜索了由胃癌转移引起的肺肿瘤栓塞病例,并提取了相关病例。然后,我们对提取的病例进行了组织切片,不仅进行了光镜观察,还对选定的 PTTM 病例进行了形态计量学分析。
有 6 例尸检涉及 PTTM,总结了它们的临床病理数据。在 4 例中,肺动脉直径与狭窄率之间存在显著的负相关。尽管所有病例都在一定程度上显示出狭窄率的增加,但狭窄率的程度因病例而异。在 4 例中,平均狭窄率在 100μm 以下组或 100-300μm 组与 300μm 组之间存在显著差异。然而,在所有病例中,100μm 以下组与 100-300μm 组之间的平均狭窄率没有显著差异。同时,所有病例的组织因子(TF)均呈阳性反应,5 例血管内皮生长因子(VEGF)呈阳性反应,3 例骨桥蛋白(OPN)呈阳性反应。
在本研究中,我们揭示了肺动脉的管腔狭窄程度因病例而异,我们的结果表明,PTTM 中的肺动脉高压发生在具有广泛肺病变且较小动脉管腔严重狭窄的选定病例中。此外,我们的免疫组织化学检查表明,提示 PTTM 的胃癌比典型胃癌的 TF 阳性率更高。然而,通过免疫组织化学确定提示 PTTM 的胃癌是否具有更高的 VEGF 或 OPN 阳性率仍然不清楚。