Kojimahara K, Mukai M, Yamazaki K, Yamada T, Katayama T, Nakada K, Uematsu S, Umezono A, Hosoda Y
Department of Pathology, Keio University School of Medicine, Tokyo, Japan.
Acta Pathol Jpn. 1993 Jan-Feb;43(1-2):65-70. doi: 10.1111/j.1440-1827.1993.tb02916.x.
A large, poorly demarcated, elevated lesion over the area ranging from the lower end of the esophagus to the lesser curvature of the cardiac region was examined in a 19 year old woman, and demonstrated an irregular and highly infiltrative proliferation of spindle cells over the full thickness of the gastric wall. Although the spindle cells grew mainly in the submucosa, they penetrated the muscularis propria, leaving intact muscle tissue that formed an irregular, island-like pattern, and reached the subserosa. The cells were identified as myofibroblasts by light microscopy, immunohistochemistry and electron microscopy. The present case is considered to be of an inflammatory pseudotumor due to extremely infiltrative growth of myofibroblasts. This lesion differed from inflammatory fibroid polyp (similarly consisting of proliferating myofibroblasts accompanied by inflammatory cells) in terms of age at onset, tumor size, pattern of cell proliferation and main inflammatory cell component. This report also discusses the relationship between this lesion and a very recently advocated new entity, inflammatory fibrosarcoma of the mesentery and retroperitoneum, which is a tumour closely simulating inflammatory pseudotumor.
对一名19岁女性进行检查,发现其食管下端至贲门区小弯处有一个界限不清的大的隆起性病变,病变显示胃壁全层有梭形细胞不规则且高度浸润性增生。虽然梭形细胞主要生长在黏膜下层,但它们穿透固有肌层,使完整的肌肉组织形成不规则的岛状形态,并到达浆膜下层。通过光学显微镜、免疫组织化学和电子显微镜鉴定这些细胞为肌成纤维细胞。由于肌成纤维细胞的极度浸润性生长,本病例被认为是炎症性假瘤。该病变在发病年龄、肿瘤大小、细胞增殖模式和主要炎症细胞成分方面与炎症性纤维瘤性息肉(同样由增殖的肌成纤维细胞伴有炎症细胞组成)不同。本报告还讨论了该病变与最近新提出的一种实体——肠系膜和腹膜后炎症性纤维肉瘤之间的关系,后者是一种与炎症性假瘤极为相似的肿瘤。