Liau C T, Jung S M, Lim K E, Shih H N
Department of Internal Medicine, Chang Gung Memorial Hospital, Taipei, Taiwan.
Jpn J Clin Oncol. 2000 Jan;30(1):37-9. doi: 10.1093/jjco/hyd005.
Pulmonary lymphangitic sarcomatosis (PLS) is not much recognized clinically although it shows similar pathological patterns and diagnostic features to pulmonary lymphangitic carcinomatosis (PLC). We report a case with hand angiosarcoma whose chest X-ray findings revealed a diffuse interstitial pattern consistent with lymphangitic spreading. The final diagnosis was made by open lung biopsy. The clinical, diagnostic and pathological features of this disease process are reviewed.
肺淋巴管肉瘤病(PLS)在临床上并不为人们所熟知,尽管它与肺淋巴管癌病(PLC)具有相似的病理模式和诊断特征。我们报告一例手部血管肉瘤患者,其胸部X线检查结果显示出与淋巴管播散一致的弥漫性间质模式。最终通过开胸肺活检做出诊断。本文对该疾病过程的临床、诊断和病理特征进行了综述。