Miller K A, Rubnitz M E, Roth S I
Laboratory Service, Veterans Administration Lakeside Medical Center, Chicago, Ill.
Arch Pathol Lab Med. 1988 Jan;112(1):86-90.
A recurrence of a gastric epithelioid stromal tumor (leiomyoblastoma) 33 years after incomplete resection and radiation therapy is reported. The original tumor involved the posterior gastric wall and presented with intraperitoneal hemorrhage. A tumor recurrence was found attached to the stomach with invasion through the wall of the splenic flexure of the colon. The histologic features of the tumor had not significantly altered, except for a slight increase in mitotic rate. Neither the original tumor nor the recurrence exhibited smooth-muscle differentiation on ultrastructural or immunohistochemical examination, suggesting an origin from an undifferentiated or primitive mesenchymal cell. The term leiomyoblastoma, although established in the literature, should be reserved for epithelioid tumors in which myoid differentiation can be established. The long interval to recurrence supports the suggestion that all of these tumors have at least a low-grade malignant potential.
本文报道了1例胃上皮样间质瘤(平滑肌瘤样细胞瘤),在不完全切除及放疗33年后复发。原发肿瘤累及胃后壁,表现为腹腔内出血。复发肿瘤附着于胃,侵犯结肠脾曲肠壁。除有丝分裂率略有增加外,肿瘤的组织学特征无明显改变。超微结构及免疫组化检查显示,原发肿瘤及复发肿瘤均未表现出平滑肌分化,提示其起源于未分化或原始间充质细胞。尽管文献中已确立“平滑肌瘤样细胞瘤”这一术语,但应仅用于可确定有肌样分化的上皮样肿瘤。复发间隔时间长支持所有这些肿瘤至少具有低度恶性潜能这一观点。