Shahid M, Siddiqi A
Department of Pathology University of Florida College of Medicine, Jacksonville, USA.
Pathologica. 2017 Dec;109(4):375-378.
Collision tumors represent a coexistence of two adjacent but histologically distinct tumors without histologic admixture in an organ. Primary well differentiated neuroendocrine tumor of ovary is rare and coexistent borderline mucinous tumor makes this association extremely rare. Although these tumors have been reported in other organs, its occurrence in ovary is rare. Collision tumor comprising primary neuroendocrine tumor of ovary and mucinous borderline tumor is an extremely rare occurrence. Here we report a case of this collision tumor in a postmenopausal female. H&E and immunohistochemical stains for chromogranin, synaptophysin, CDX-2, CK20, CK7 and Ki-67 were performed to confirm the diagnosis of collision tumor. Extensive search of literature revealed only a couple of cases report so far with this association. Our case is unique for a reason that we have reported trabecular variant of neuroendocrine tumor while the previously reported cases were insular variant. Management depends on patient's age, desire for fertility and disease distribution.
碰撞瘤是指在一个器官中,两种相邻但组织学上不同的肿瘤并存,且不存在组织学混合。卵巢原发性高分化神经内分泌肿瘤罕见,并存的交界性黏液性肿瘤使这种关联极为罕见。尽管这些肿瘤在其他器官中已有报道,但其在卵巢中的发生却很罕见。由卵巢原发性神经内分泌肿瘤和黏液性交界性肿瘤组成的碰撞瘤极为罕见。在此,我们报告一例绝经后女性的这种碰撞瘤病例。进行了苏木精-伊红染色以及嗜铬粒蛋白、突触素、CDX-2、细胞角蛋白20、细胞角蛋白7和Ki-67的免疫组化染色,以确诊碰撞瘤。广泛查阅文献发现,迄今为止仅有几例关于这种关联的病例报告。我们的病例具有独特性,因为我们报告的是神经内分泌肿瘤的小梁状变体,而先前报告的病例是岛状变体。治疗方案取决于患者的年龄、生育意愿和疾病分布情况。