Updates in Pathology for Retroperitoneal Soft Tissue Sarcoma

被引:22
作者
Mack, Tanner [1 ,2 ]
Purgina, Bibianna [1 ,2 ]
机构
[1] Univ Ottawa, Ottawa Hosp, Dept Pathol & Lab Med, Ottawa, ON K1H 8L6, Canada
[2] Eastern Ontario Reg Lab Assoc EORLA, Ottawa, ON K1H 8L6, Canada
关键词
retroperitoneum; sarcoma; molecular; liposarcoma; leiomyosarcoma; GIST; malignant peripheral nerve sheath tumor; solitary fibrous tumor; pathology; NERVE SHEATH TUMORS; WELL-DIFFERENTIATED LIPOSARCOMA; CARNEY-STRATAKIS-SYNDROME; SMOOTH-MUSCLE TUMORS; LIPOMATOUS TUMORS; DEDIFFERENTIATED LIPOSARCOMAS; MOLECULAR-GENETICS; STROMAL TUMORS; CELL TUMORS; ANGIOSARCOMA;
D O I
10.3390/curroncol29090504
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Retroperitoneal tumors are extremely rare. More than 70% of primary retroperitoneal soft tissue tumors are malignant. The most common sarcomas in the retroperitoneum include liposarcomas and leiomyosarcoma, however other sarcomas, along with benign mesenchymal tumors, can occur. Sarcomas are a heterogenous group of tumors with overlapping microscopic features, posing a diagnostic challenge for the pathologist. Correct tumor classification has become important for prognostication and the evolving targeted therapies for sarcoma subtypes. In this review, the pathology of retroperitoneal soft tissue sarcomas is discussed, which is important to the surgical oncologist. In addition, less common sarcomas and benign mesenchymal tumors of the retroperitoneum, which may mimic sarcoma clinically and pathologically, are also discussed.
引用
收藏
页码:6400 / 6418
页数:19
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