Huan Youming, Idrees Muhammad, Gribetz Michael E, Unger Pamela D
Department of Pathology, Mount Sinai Medical Center, New York, P.O. Box 1194, New York, NY 10029, USA.
Ann Diagn Pathol. 2008 Apr;12(2):142-5. doi: 10.1016/j.anndiagpath.2006.08.008. Epub 2007 Aug 17.
We report 2 patients with conventional prostatic adenocarcinoma who developed sarcomatoid carcinoma of probable prostatic origin 6 and 2.5 years after radiation treatment (seed implantation and external beam). Our cases had histologic features consistent with those cases previously reported in the literature. The tumors consisted of spindle cells with large hyperchromatic nuclei and a pattern mimicking a sarcoma. Immunohistochemical studies showed the tumors to be weakly positive for EMA, CK7, and vimentin. Ki67 staining showed positivity in more than 50% of tumor cells. The tumors also stained diffusely positive for p53 and p63. PSA and PAP were negative. Clinically, the sarcomatoid carcinomas appeared to be of prostatic origin. The pathogenesis of the tumors is still uncertain but most likely represent a radiation-induced dedifferentiation of prostatic adenocarcinoma.
我们报告2例常规前列腺腺癌患者,他们在放射治疗(粒子植入和外照射)后6年和2.5年发生了可能起源于前列腺的肉瘤样癌。我们的病例具有与先前文献报道的病例一致的组织学特征。肿瘤由具有大的深染核的梭形细胞组成,其模式类似肉瘤。免疫组织化学研究显示肿瘤对上皮膜抗原(EMA)、细胞角蛋白7(CK7)和波形蛋白呈弱阳性。Ki67染色显示超过50%的肿瘤细胞呈阳性。肿瘤对p53和p63也呈弥漫性阳性染色。前列腺特异性抗原(PSA)和前列腺酸性磷酸酶(PAP)为阴性。临床上,肉瘤样癌似乎起源于前列腺。肿瘤的发病机制仍不确定,但很可能代表前列腺腺癌的辐射诱导去分化。