Sato N, Zaloudek C, Geelhoed G W, Orenstein J M
Arch Pathol Lab Med. 1984 Feb;108(2):164-7.
We present the clinical and pathologic features of a malignant mesenchymoma of the small intestine. Light and electron microscopic studies of the sarcoma revealed multiple patterns of differentiation, including fibrosarcoma, leiomyosarcoma, chondrosarcoma, and osteosarcoma. A recurrence had the morphologic nature of a mesenchymal chondrosarcoma. Clinically, the neoplasm was not detected by barium contrast radiography, but it was readily defined by sonography and computed tomography. Despite aggressive surgery and chemotherapy, the patient died 15 months after the diagnosis was made.
我们报告了一例小肠恶性间叶瘤的临床和病理特征。对该肉瘤进行的光镜和电镜研究显示出多种分化模式,包括纤维肉瘤、平滑肌肉瘤、软骨肉瘤和骨肉瘤。一次复发具有间叶性软骨肉瘤的形态学特征。临床上,钡剂造影未能检测到该肿瘤,但超声检查和计算机断层扫描很容易对其进行界定。尽管采取了积极的手术和化疗措施,患者在确诊后15个月死亡。