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巨细胞型钙化性支持细胞瘤:采用组织形态学、免疫组织化学、超微结构、比较基因组杂交和 PRKAR1A 基因聚合酶链反应分析研究 1 例恶性和 3 例良性肿瘤的临床病理。

Large cell calcifying Sertoli cell tumor: a clinicopathologic study of 1 malignant and 3 benign tumors using histomorphology, immunohistochemistry, ultrastructure, comparative genomic hybridization, and polymerase chain reaction analysis of the PRKAR1A gene.

机构信息

Department of Pathology, National University Health System, Singapore 119074, Singapore.

出版信息

Hum Pathol. 2010 Apr;41(4):552-9. doi: 10.1016/j.humpath.2009.09.008. Epub 2009 Dec 11.

Abstract

Four cases of large cell calcifying Sertoli cell tumor, 3 benign and 1 malignant, with no clinical signs of Carney complex or Peutz-Jeghers syndrome are reported with results of histologic, immunohistochemical, ultrastructural, and comparative genomic hybridization studies. Analysis of PRKAR1A gene was performed on 2 cases. The age range of the patients was 19 to 54 years. The patient with a malignant large cell calcifying Sertoli cell tumor died of disease 4 years after surgery. Patients with benign tumors have had an uneventful follow-up for 1 and 3 years. All tumors were well circumscribed, unencapsulated, and composed of solid sheets, irregular cords, tubular structures, and nests in a fibrous and/or myxoid stroma with cellular atypia in the malignant case. All tumors showed diffuse immunoreactivity for inhibin, vimentin, calretinin, and S100 protein. Focal positivity for cytokeratin (AE1/AE3) was noticed in 1 case. Tumors were negative for CAM 5.2, Mic-2, Melan-A laminin, placental alkaline phosphatase, and alpha-fetoprotein. The proliferation index was 5% and 10% for 2 of the benign tumors and 30% for the malignant tumor. Comparative genomic hybridization was performed in 2 cases. There was no evidence of any major chromosomal changes. In one case, no PRKAR1A gene mutation was found. In the other case, a heterozygous shift mutation c.65_84dup was found, despite the absence of other clinical signs of Carney complex or Peutz-Jeghers syndrome. Although the combination of large cell calcifying Sertoli cell tumor and PRKAR1A mutation fulfills the criteria for establishing a diagnosis of Carney complex, the clinical relevance of finding a PRKAR1A gene mutation in a patient without any clinical signs of Carney complex or Peutz-Jeghers syndrome remains to be established.

摘要

报告了 4 例大细胞钙化性支持细胞瘤,3 例为良性,1 例为恶性,均无卡尼复合征或皮杰氏综合征的临床征象,并进行了组织学、免疫组织化学、超微结构和比较基因组杂交研究。对 2 例病例进行了 PRKAR1A 基因分析。患者年龄为 19-54 岁。患有恶性大细胞钙化性支持细胞瘤的患者在手术后 4 年内死于疾病。良性肿瘤患者的随访时间分别为 1 年和 3 年,均无异常。所有肿瘤均边界清楚,无包膜,由实性片层、不规则索状、管状结构和巢状结构组成,在恶性病例中可见细胞异型性,伴有纤维和/或黏液样基质。所有肿瘤均弥漫性表达抑制素、波形蛋白、钙视网膜蛋白和 S100 蛋白。1 例病例中发现细胞角蛋白(AE1/AE3)局灶性阳性。肿瘤对 CAM5.2、Mic-2、Melan-A 层粘连蛋白、胎盘碱性磷酸酶和α-胎蛋白均为阴性。2 例良性肿瘤的增殖指数为 5%和 10%,而恶性肿瘤为 30%。对 2 例病例进行了比较基因组杂交。没有发现任何主要染色体变化。在 1 例病例中未发现 PRKAR1A 基因突变。在另 1 例病例中,发现了杂合性移码突变 c.65_84dup,尽管没有卡尼复合征或皮杰氏综合征的其他临床征象。尽管大细胞钙化性支持细胞瘤与 PRKAR1A 突变的组合符合建立卡尼复合征诊断的标准,但在无卡尼复合征或皮杰氏综合征临床征象的患者中发现 PRKAR1A 基因突变的临床意义仍有待确定。

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