需要免疫组化诊断的眼睑皮脂腺癌的临床病理特征

IF 0.9 Q4 OPHTHALMOLOGY
Ocular Oncology and Pathology Pub Date : 2024-09-01 Epub Date: 2024-04-29 DOI:10.1159/000538537
Tatsuya Yunoki, Akio Miyakoshi, Atsushi Hayashi
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引用次数: 0

摘要

简介:该研究旨在评估眼睑皮脂腺癌(SGC)的临床病理特征:该研究旨在评估眼睑皮脂腺癌(SGC)的临床病理特征,明确诊断需要进行免疫组化检查:回顾性研究2016年4月至2022年4月期间富山大学医院最终诊断为眼睑皮脂腺癌的27例患者。在临床强烈怀疑为SGC的病例中,如果苏木精-伊红染色的初步病理诊断为非SGC,则进行额外的详细病理检查,包括嗜脂肪蛋白(ADP)和雄激素受体(AR)的免疫染色:五名患者(18.5%)的诊断结果与 SGC 无关,其中三人患有鳞状细胞癌(SCC),一人患有基底细胞癌,一人患有鲍温病。对这 5 例患者再次进行了详细的病理检查,包括 ADP 和 AR 的免疫染色,最终确诊为 SGC。所有 5 个病例的 ADP 均呈阳性,4 个病例的 AR 呈阳性。被诊断为 SCC 的 3 例患者的特点是 Ki-67 指数高、有丝分裂活跃、分化程度相对较低:结论:SGC 可以在其他癌症(如 SCC 和 BCC)中进行病理诊断。结论:SGC可被病理诊断为其他癌症,如SCC和BCC。ADP和AR的免疫染色对确诊SGC非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinicopathologic Features of Eyelid Sebaceous Gland Carcinoma Requiring Immunohistochemical Diagnosis.

Introduction: The aim of the study was to evaluate the clinicopathological features of eyelid sebaceous gland carcinoma (SGC), which requires immunohistochemical examination for a definitive diagnosis.

Methods: Twenty-seven patients with a final diagnosis of eyelid SGC at Toyama University Hospital between April 2016 and April 2022 were retrospectively studied. In cases with a strong clinical suspicion of SGC, if the initial pathological diagnosis by hematoxylin-eosin staining was non-SGC, additional detailed pathology was performed, including immunostaining for adipophilin (ADP) and androgen receptor (AR).

Results: Five patients (18.5%) had a diagnosis other than SGC, including three with squamous cell carcinoma (SCC), one with basal cell carcinoma, and one with Bowen disease. In these 5 cases, detailed pathology, including immunostaining for ADP and AR, was performed again, which ultimately led to the diagnosis of SGC. ADP was positive in all 5 cases, and AR was positive in 4 cases. The 3 patients diagnosed with SCC were characterized by a high Ki-67 index, active mitosis, and relatively low differentiation.

Conclusion: SGC can be pathologically diagnosed in other cancers, such as SCC and BCC. When SCC was diagnosed, it was often hypo-differentiated and required more attention. Immunostaining for ADP and AR is invaluable for confirming SGC diagnosis.

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CiteScore
2.40
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