SALL4 Is a Novel Sensitive and Specific Marker of Ovarian Primitive Germ Cell Tumors and Is Particularly Useful in Distinguishing Yolk Sac Tumor From Clear Cell Carcinoma

被引:149
作者
Cao, Dengfeng [1 ]
Guo, Shuangping [4 ]
Allan, Robert W. [2 ]
Molberg, Kyle H. [3 ]
Peng, Yan [3 ]
机构
[1] Washington Univ, Lauren V Ackerman Lab Surg Pathol, Div Anat & Mol Pathol, Dept Pathol & Immunol,Sch Med, St Louis, MO 63110 USA
[2] Univ Florida, Dept Pathol, Gainesville, FL 32611 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
[4] Fourth Mil Med Univ, Dept Pathol, Xijing Hosp, Xian 710032, Shanxi Province, Peoples R China
关键词
SALL-4; ovary; germ cell tumor; yolk sac tumor; clear cell carcinoma; ENDODERMAL SINUS TUMOR; EMBRYONIC STEM-CELLS; ALPHA-FETOPROTEIN; ENDOMETRIOID CARCINOMA; DIFFERENTIAL-DIAGNOSIS; POSTMENOPAUSAL WOMAN; OKIHIRO-SYNDROME; HOMEOTIC GENE; PLURIPOTENCY; EXPRESSION;
D O I
10.1097/PAS.0b013e318198177d
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Ovarian primitive germ cell tumors (GCTs) are uncommon tumors and sometimes pose diagnostic challenges. Among them, yolk sac tumor (YST) poses the greatest diagnostic difficulty and can be mistaken for clear cell carcinoma (CCC). Current immunohistochemical markers Such as alpha-fetoprotein (AFP), glypican-3. cytokeratin (CK) 7, and epithelial membrane antigen (EMA) used to distinguish YST from CCC lack adequate sensitivity and specificity. Here by immunohistochemistry. we investigated a novel marker SALL4 in 98 GCTs (29 YSTs, 18 dysgerminomas. 6 gonadoblastomas, 6 embryonal carcinomas, 15 immature and 12 Mature teratomas. 7 carcinoid tumors, 3 strumal carcinoids, and 2 struma ovarii) with particular interest of exploring SALL4 to distinguish YST from CCC. One hundred sixty-three non-GCTs including 45 CCCs were also stained. We found that SALL4 is strongly positive in more than 90% tumor cells in all YSTs, dysgerminomas, gonadoblastomas, and embryonal carcinomas. Variable SALL4 staining is seen in 11 of 15 immature teratomas. All other GCTs included in this Study are negative for SALL4. Except 3 CCCs with focal SALL4 staining (< 15% tumor cells), SALL4 is negative in the remaining 160 non-GCTs. We also compared SALL4 with AFP, glypican-3, CK7, and EMA in all YSTs and CCCs. AFP and glypican-3 are positive in 24 (83%) and 20 (69%) YSTs, respectively, whereas 16 (35%) and 13(28%) CCCs show positive AFP and glypican-3 staining, respectively. Three (10%) and 4 (14%) YSTs show focal (< 21% tumor cells) CK7 and EMA staining, respectively. CK7 and EMA are positive in all 45 CCCs but 3 (7%) and 1 (2%) cases show staining in less than 30% tumor cells, respectively. Our findings indicate that SALL4 is a novel sensitive and specific marker for ovarian primitive GCTs. SALL4 is particularly useful in distinguishing YST from CCC and better than AFP., glypican-3, CK7, and EMA.
引用
收藏
页码:894 / 904
页数:11
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