Schraufnagel D E, Sekosan M, McGee T, Thakkar M B
Dept of Medicine, University of Illinois at Chicago 60612-7323, USA.
Eur Respir J. 1996 Feb;9(2):346-50. doi: 10.1183/09031936.96.09020346.
The bronchial circulation undergoes angiogenesis in several pathological conditions, such as lung neoplasm and bronchiectasis, but whether the pulmonary circulation can do this has been questioned. A woman treated with mitomycin C and 5-fluorouracil developed progressive, fatal pulmonary hypertension over 5 months. In addition to light and transmission electron microscopic examination of her lung, her pulmonary vasculature was cast and the casts were studied with scanning electron microscopy. Light microscopy showed that she had pulmonary veno-occlusive disease and angiomatoid capillary growth in the alveolar walls. Transmission electron microscopy confirmed the presence of pulmonary hypertension and showed thickened endothelial basement membrane. Scanning electron microscopy of the cast blood vessels showed distortion and destruction of alveolar capillaries prohibiting the passage of erythrocytes. Large new capillaries developed on top of, and were connected to, the shrivelled capillaries that made up the alveolar wall. The new capillaries were larger and fewer, which reduced the alveolar-capillary interface. Arteries and veins were irregularly narrowed and the veins had broad muscularity. Oedema was present, and the pulmonary lymphatics were extensively cast, especially in the lobular septa, but the lymphatics had a normal appearance. It appears that this patient suffered extensive capillary damage and venous occlusion and that the response was extensive new capillary formation, sometimes in angiomatoid configurations, and hypertrophy of pulmonary veins and arteries. Casting the microvasculature and viewing it with scanning electron microscopy identified new alveolar capillaries in this patient with acquired pulmonary hypertension.
支气管循环在几种病理状态下会发生血管生成,如肺部肿瘤和支气管扩张,但肺循环是否能如此一直存在疑问。一名接受丝裂霉素C和5-氟尿嘧啶治疗的女性在5个月内出现进行性、致命性肺动脉高压。除了对她的肺进行光镜和透射电镜检查外,还对其肺血管系统进行铸型,并通过扫描电镜对铸型进行研究。光镜显示她患有肺静脉闭塞性疾病以及肺泡壁上的血管瘤样毛细血管生长。透射电镜证实存在肺动脉高压,并显示内皮基底膜增厚。铸型血管的扫描电镜显示肺泡毛细血管扭曲和破坏,阻止红细胞通过。在构成肺泡壁的皱缩毛细血管之上形成并与之相连的大的新毛细血管。新毛细血管更大但数量更少,这减少了肺泡-毛细血管界面。动脉和静脉不规则狭窄,静脉有广泛的肌层。存在水肿,肺淋巴管广泛铸型,尤其是在小叶间隔,但淋巴管外观正常。看来该患者遭受了广泛的毛细血管损伤和静脉闭塞,其反应是广泛的新毛细血管形成,有时呈血管瘤样形态,以及肺静脉和动脉肥大。对微血管系统进行铸型并用扫描电镜观察,在这名获得性肺动脉高压患者中发现了新的肺泡毛细血管。