卵巢肿块中的腹水,特别是配对盒基因 8 的免疫表达:横断面分析

Prabhat Mahato, Chhanda Das, Rama Saha, Ankita Pranab Mandal, Gourisankar Kamilya
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引用次数: 0

摘要

由于诊断较晚,卵巢恶性肿瘤的死亡率很高。早期准确诊断可改善针对具体病例的治疗。事实证明,配对盒基因 8(PAX8)可在卵巢上皮细胞中表达,被认为是早期诊断的新生物标志物。病例对照研究表明,PAX8 在血清中的水平与组织表达呈正相关,在卵巢恶性肿瘤中,尤其是在卵巢恶性肿瘤中最常见的高级别浆液性卵巢恶性肿瘤中,PAX8 的水平会升高。 本研究的目的是评估卵巢肿瘤病变的流行病学谱,并比较研究传统细胞学和腹水细胞块以及随后的 PAX8 免疫组织化学(IHC)表达来诊断卵巢肿瘤。 我们使用预先设计的表格收集参与者的临床数据。我们使用传统细胞学方法进行细胞学诊断,然后制备细胞块,随后评估 PAX8 IHC 表达。用于制备细胞块的腹水经离心后,将组织沉淀物与血浆混合,然后滴加凝血酶。我们加入 10% 福尔马林固定凝血样本 30 分钟。将福尔马林固定、石蜡包埋的细胞块切成 4-5 μ 的切片,并用苏木精和伊红染色。随后,我们用免疫组化染色法检测 PAX8 的表达,以诊断卵巢恶性肿瘤。 我们收到了 55 份腹水样本。在细胞学涂片检查中,12 例(21.8%)为良性,35 例(63.6%)为恶性,其余 8 例(14.6%)为可疑恶性。在细胞块制备的组织学检查中,43 例(78.2%)为恶性病例,在这 43 例细胞块研究病例中,37 例 PAX8 呈阳性;6 例 PAX8 呈阴性。恶性细胞阳性与细胞块中的 PAX8 状态有统计学意义(P < 0.001)。 对于可能从靶向治疗中获益的高级别卵巢癌患者,应考虑对腹水细胞块研究中的 PAX8 状态进行评估。卵巢肿块和腹水患者可在腹水细胞学检查中评估PAX8状态,以便进行新辅助化疗。
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Ascitic Fluid in Ovarian Mass with Special Reference to Paired-box Gene 8 Immunoexpression: A Cross-sectional Analysis
Mortality in the case of ovarian malignancy is high due to late diagnosis. Early and accurate diagnosis can improve case-specific management. Paired-box gene 8 (PAX8) has proved to be expressed in the ovarian epithelial cells and is considered a new biomarker for early diagnosis. Case–control studies show that the level of PAX8 in the serum and tissue expressions are positively correlated and increased in ovarian malignancy, especially in the high-grade serous type, the most common variety of ovarian malignancies. The aim of this study was to assess the epidemiological spectrum of ovarian neoplastic lesions and a comparative study of conventional cytology and a cellblock of ascitic fluid and subsequent PAX8 immunohistochemistry (IHC) expression to diagnose ovarian neoplasm. We collected clinical data from participants using a predesigned pro forma. We made a cytological diagnosis using conventional cytology, followed by cellblock preparation and subsequent assessment of PAX8 IHC expression. Ascitic fluid received for cellblock was centrifuged, tissue sediment was mixed with plasma, and then drops of thrombin were added. We fixed the clotted sample by adding 10% formalin for 30 min. The formalin-fixed, paraffin-embedded cellblocks were sliced into 4–5 μ sections and stained with hematoxylin and eosin. Subsequently, we used an immunohistochemical stain for PAX8 expression to diagnose ovarian malignancy. We received 55 ascitic fluid samples. On cytological smear examination, 12 (21.8%) cases were benign, 35 (63.6%) were malignant, and the remaining 8 (14.6%) were suspicious of malignancy. On histological examination of cellblock preparation, 43 (78.2%) were malignant cases, and among these 43 cases of cellblocks studied, 37 were positive for PAX8 status; six were negative for PAX8. There was a statistically significant association between malignant cell positivity and PAX8 status in the cellblock (P < 0.001). An evaluation of PAX8 status in ascitic fluid cellblock study should be considered for high-grade ovarian cancers in patients who may benefit from targeted therapies. Patients with ovarian mass and ascites can be evaluated for PAX8 status in their ascitic fluid cytology study for the purpose of neoadjuvant chemotherapy.
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