Vajó J, Böör A, Sokol L, Rezucha M, Kundrát I, Stebnický M, Holecko R
II. chirurgická klinika FN L. Pasteura, LF UPJS, Kosice.
Rozhl Chir. 1994 Nov;73(7):339-41.
The authors present a report on a new clinical and pathological entity--aggressive angiomyxoma which was described in 1983. They draw attention to the genesis of this tumour and its macro- and microscopic picture. They emphasize that treatment of this tumour involves its complete surgical extirpation and frequent local relapses without secondaries. The authors describe in detail two of their observations of aggressive angiomyxoma in a 32- an 38-year-old woman where the tumour started in the lesser pelvis. In both instances, despite radical extirpation of the tumour, within a relatively short time a local relapse developed detected by USG and CT without clinical symptoms.
作者发表了一篇关于一种新的临床和病理实体——侵袭性血管黏液瘤的报告，该肿瘤于1983年被描述。他们提请注意这种肿瘤的起源及其大体和显微镜下表现。他们强调，这种肿瘤的治疗包括完整的手术切除，且常出现局部复发但无转移。作者详细描述了他们对两名侵袭性血管黏液瘤患者的观察，一名32岁，另一名38岁，肿瘤均起源于小骨盆。在这两个病例中，尽管肿瘤被彻底切除，但在相对较短的时间内，超声和CT检查发现了局部复发，且无临床症状。
