Department of Pathology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu Province, 210029, China.
Diagn Pathol. 2024 May 27;19(1):71. doi: 10.1186/s13000-024-01496-z.
Current diagnostic criteria of adrenocortical neoplasms are mostly based on morphology. The utility of immunohistochemistry (IHC) and histochemistry is limited.
To evaluate the diagnostic and prognostic utility of clinicopathological features, morphology, ancillary biomarkers, and reticular histochemistry in adrenocortical neoplasms. We examined 28 adrenocortical carcinomas (ACCs) and 50 adrenocortical adenomas (ACAs) obtained from pathology archives. Clinical data were retrieved from medical records. Two pathologists independently assessed hematoxylin and eosin-stained slides, employing modified Weiss criteria for all tumors and Lin-Weiss-Bisceglia criteria for oncocytic variants. Immunohistochemical markers (Calretinin, alpha-inhibin, MelanA, SF-1, Ki-67, PHH3, IGF-2, β-catenin, P53, CYP11B1, CYP11B2, MLH1, MSH2, MSH6, PMS2, EPCAM) and Gomori's Silver histochemistry were applied. Statistical analysis utilized SPSS Statistics 26.
ACCs exhibited larger tumor sizes (P<0.001) and symptomatic presentations (P = 0.031) compared to ACAs. Parameters of modified Weiss criteria and angioinvasion demonstrated diagnostic value for ACCs. Six immunohistochemical antibodies((MelanA, Ki-67, IGF-2, β-catenin, P53 and CYP11B1) and reticulin framework alterations showed diagnostic value. Notably, Ki-67 and reticulin staining were most recommended. Evident reticulin staining was frequently present in ACCs (P<0.001). Ki-67 was significantly higher in ACCs (P<0.001). Twenty-one conventional and seven oncocytic entities showed different necrosis frequencies. Symptoms and Ki-67 index ≥ 30% were prognostic for ACCs, correlating with shorter survival.
This study emphasizes the diagnostic value of reticulin framework alterations and a high Ki-67 index. Markers such as CYP11B1, IGF2, P53, β-catenin and MelanA also contribute to the diagnosis of ACCs. Symptoms and Ki-67 index ≥ 30% predict shorter survival. These findings encourges the use of ancillary markers such as reticulin histochemistry and Ki-67 in the workup of evaluations of adrenocortical neoplasms.
目前肾上腺皮质肿瘤的诊断标准主要基于形态学。免疫组织化学(IHC)和组织化学的应用有限。
评估临床病理特征、形态学、辅助生物标志物和网状组织化学在肾上腺皮质肿瘤中的诊断和预后价值。我们检查了 28 例肾上腺皮质癌(ACC)和 50 例肾上腺皮质腺瘤(ACA),这些病例均来自病理档案。临床数据从病历中检索。两位病理学家分别使用改良 Weiss 标准评估所有肿瘤和 Lin-Weiss-Bisceglia 标准评估嗜酸细胞变异体的苏木精和伊红染色切片。应用免疫组织化学标志物(钙结合蛋白、α-抑制素、黑素 A、SF-1、Ki-67、PHH3、IGF-2、β-连环蛋白、P53、CYP11B1、CYP11B2、MLH1、MSH2、MSH6、PMS2、EPCAM)和 Gomori 银染色。统计分析采用 SPSS Statistics 26。
ACC 组肿瘤体积较大(P<0.001),症状表现更为明显(P=0.031)。改良 Weiss 标准参数和血管侵犯对 ACC 具有诊断价值。六种免疫组织化学抗体(黑素 A、Ki-67、IGF-2、β-连环蛋白、P53 和 CYP11B1)和网状纤维框架改变具有诊断价值。值得注意的是,Ki-67 和网状纤维染色最具推荐价值。明显的网状纤维染色在 ACC 中很常见(P<0.001)。Ki-67 在 ACC 中明显升高(P<0.001)。21 例常规型和 7 例嗜酸细胞型实体瘤的坏死频率不同。症状和 Ki-67 指数≥30%对 ACC 具有预后意义,与生存时间缩短相关。
本研究强调了网状纤维框架改变和高 Ki-67 指数的诊断价值。CYP11B1、IGF2、P53、β-连环蛋白和黑素 A 等标志物也有助于 ACC 的诊断。症状和 Ki-67 指数≥30%预测生存时间更短。这些发现鼓励在评估肾上腺皮质肿瘤时使用辅助标志物,如网状组织化学和 Ki-67。