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Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature

机译：具有异型肉瘤成分的成人型睾丸颗粒细胞瘤：病例报告和文献复习

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Thomas EO Schubert; Robert Stoehr; Arndt Hartmann; Sabrina Schöne; Mathias Löbelenz; Gregor Mikuz;
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1. Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature [J] . Thomas EO Schubert, Robert Stoehr, Arndt Hartmann, Diagnostic pathology . 2014,第S1期

机译：异型肉瘤成分的成人型睾丸颗粒细胞瘤：病例报告及文献复习
2. Adult type granulosa cell tumor in adult testis: report of a case and review of the literature [J] . Zhao Song, David J. Vaughn, Zhanyong Bing Rare tumors . 2011,第4期

机译：成人睾丸中的成人型颗粒细胞瘤：一例报道并文献复习
3. Adult Type Granulosa Cell Tumor: A Very Rare Case of Sex-Cord Tumor of the Testis with Review of the Literature [J] . DimosthenisMiliaras, EleftheriosAnagnostou, IoannisMoysides Case Reports in Pathology . 2013,第3期

机译：成年型颗粒细胞肿瘤：睾丸性线性肿瘤非常罕见的病例与文献综述。
4. Acute disseminated encephalomyelitis with peripheral nervous system involvement in an adult following measles: a case report and review of literature [C] . Ying Zhang, Panpan Zhao, Huiyi Jiang, International Conference on Medical Engineering and Bioinformatics . 2015

机译：急性播散脑髓炎，外周神经系统参与成年人的麻疹：案例报告和文学审查
5. Characterization of anti-Mullerian Hormone in the Stallion and Mare: Changes During Testis Development and Determination of Serum Concentrations in Normal Mares, Pregnant Mares and Mares with Granulosa-cell Tumors. [D] . Almeida, Juliana Lopes. 2010

机译：种马和母马中抗穆勒激素的特性：睾丸发育过程中的变化以及正常母马，孕妇母马和具有颗粒细胞瘤的母马的血清浓度测定。
6. Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature [O] . Thomas EO Schubert, Robert Stoehr, Arndt Hartmann, 2014

机译：具有异型肉瘤成分的成人型睾丸颗粒细胞瘤：病例报告和文献复习
7. Adult type granulosa cell tumor in adult testis: report of a case and review of the literature [O] . Song, Zhao, Vaughn, David J., Bing, Zhanyong 2011

机译：成人睾丸中的成人型颗粒细胞瘤：一例报告并文献复习

Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature

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