Banathy L J
Pathology. 1977 Jan;9(1):65-7. doi: 10.3109/00313027709085240.
A malignant endothelial tumour arising in a congenitally lymphoedematous extremity is a sufficiently rare tumour to deserve the reporting of a new case. This tumour presented as small nodules on the back of the hand and in spite of midhumeral amputation widely scattered pulmonary metastases were present at the autopsy 28 months after the original presentation.
发生于先天性淋巴水肿肢体的恶性内皮肿瘤是一种极为罕见的肿瘤，因此报道一例新病例很有必要。该肿瘤表现为手背的小结节，尽管进行了肱骨中段截肢，但在初次发病28个月后的尸检中仍发现有广泛散在的肺转移。
