摘要
目的：探讨磷酸盐尿性间叶肿瘤的临床病理学特点。方法回顾分析10例患者的临床资料，观察10例磷酸盐尿性间叶肿瘤的形态及免疫表型。结果患者男6例，女4例，年龄范围23～55岁，平均43.1岁；患者均有1～13年骨痛、关节痛和活动困难的病史，检查发现低血磷、高尿磷；肿瘤最大径0.8～5 cm不等（平均3.05 cm）；瘤组织为间叶组织来源，可见多少不等的梭形纤维母细胞样细胞、脂肪细胞、软骨样细胞、黏液样细胞等，瘤组织富于血管，4例病变中有少见的絮状或不规则砂砾样钙盐沉积，3例发生于软组织的肿瘤周边见骨壳形成；8例细胞分裂象少见，2例核分裂象多见并且异型性明显；瘤细胞VIM及CD56阳性，7例NSE阳性，3例Bcl-2瘤细胞阳性，结蛋白、S-100、AE1/AE3均阴性，Ki-67指数8例1%～5%，仅2例为20%～30%。结论磷酸盐尿性间叶肿瘤多为良性或低度恶性的间叶组织肿瘤，因组织学多种多样而易误诊，掌握其共同的特征性并结合临床资料方能正确诊断。
Objective To study the clinicopathologic features of phosphaturic mesenchymal tumor. Methods The clinical and pathologic findings of 10 cases of phosphaturic mesenchymal tumor were evaluated. Hematoxylin and eosinstain, immunohistochemistry and histochemistry were performed on the archival paraffin sections. Results Amongst the 10 patients studied, 6 were males and 4 were females. Their age at the time of operation ranged from 23 to 55 years （mean=43.1 years）. A history of long standing bone pain, arthralgia, limitation in movement, hypophosphatemia and hyperphosphaturia was present in all cases. The duration of symptoms ranged from 1 to 13 years. The tumor size ranged from 0.8 to 5 cm （mean size=3.05 cm）. Microscopically, the tumors were composed of various mesenchymal cells, including spindled fibroblast-like cells, adipocytes, chondroid cells and mucinous cells. The background was rich in blood vessels. In 4 of the 10 cases, there was also dystrophic calcification in an unusual flocculent or“grungy”pattern. Peripheral woven bone shell formation was noted in 2 cases. Mitotic figures were rare in 5 cases. In 2 of the 10 cases however, mitotic figures and bizarre cells were commonly encountered. On immunohistochemical study, the tumor cells were all positive for vimentin and CD56. There was focal positivity for NSE and Bcl-2 in 7 and 3 cases respectively. The staining for desmin, S-100 and AE1/A E3 was negative. Ki-67 proliferation index was 1%-5%in 8 cases and 20%-30%in 2 cases. Conclusions Most of the phosphaturic mesenchymal tumors are either benign or low grade malignant mesenchymal tumors. They can be mistaken as other neoplasms due to the morphologic heterogeneity present. Thorough understanding of the associated clinical features and laboratory investigation results is helpful in arriving at the correct diagnosis.
出处
《中华临床医师杂志（电子版）》
CAS
2014年第20期20-23,共4页
Chinese Journal of Clinicians(Electronic Edition)
