孤立性纤维性肿瘤及其类似物的临床病理和免疫组织化学特征:单中心经验。

IF 1.9 Q3 PATHOLOGY
Clinical Pathology Pub Date : 2021-07-02 eCollection Date: 2021-01-01 DOI:10.1177/2632010X211028209
Bita Geramizadeh, Fatemeh Safavi
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引用次数: 3

摘要

背景:孤立性纤维性肿瘤(SFT)是一种纤维母细胞肿瘤,最初报道为胸膜肿瘤,但现在已被定义为可在人体各处可见的肿瘤。组织病理学上,许多纤维母细胞肿瘤可以模拟SFT,免疫组织化学是鉴别诊断的必要条件。已经使用了几种标记物,最近,STAT6被引入作为诊断标记物。没有来自伊朗的研究报告。目的:在这篇报告中,我们试图介绍我们在过去10年中从我们中心获得的35例SFT的临床病理发现的经验,重点是STAT6在该肿瘤中的诊断作用。患者和方法:在过去的10年中,我们在设拉子医科大学的病理档案中确认了35例SFT的诊断。这35例被认为是病例。所有的临床病理结果也从患者的临床图表中提取出来。为了评估STAT6的诊断作用,我们还从病理档案中提取了35例梭形细胞肿瘤作为SFT的模拟物。70例患者和对照组均进行STAT6染色。结果和讨论:我们的经验表明,SFT在中年男性中更为常见,年龄范围广,但在儿童中非常罕见。它可以出现在每个位置,尺寸范围从小于1厘米到大于15厘米。异常鹿角血管的存在是主要的诊断组织病理学特征之一。STAT6诊断SFT的敏感性和特异性分别为91%和86%。其他标志物如CD99、CD34和BCL2也被认为对该肿瘤的鉴别诊断有用,尽管其诊断准确性似乎低于STAT6。高有丝分裂,存在坏死和异型性是预测SFT恶性和侵袭性行为的重要标准。在我们研究的35例病例中,有17%表现为复发或转移性肿瘤的恶性行为。结论:孤立性纤维性肿瘤是一种常见的软组织肿瘤,它可以随处可见,需要仔细的组织病理学和免疫组化评价才能正确诊断和预测其侵袭性或良性行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinicopathologic and Immunohistochemical Characteristics of Solitary Fibrous Tumor and Its Mimics: A Single-Center Experience.

Clinicopathologic and Immunohistochemical Characteristics of Solitary Fibrous Tumor and Its Mimics: A Single-Center Experience.

Clinicopathologic and Immunohistochemical Characteristics of Solitary Fibrous Tumor and Its Mimics: A Single-Center Experience.

Clinicopathologic and Immunohistochemical Characteristics of Solitary Fibrous Tumor and Its Mimics: A Single-Center Experience.

Background: Solitary fibrous tumor (SFT) is a fibroblastic tumor that has been originally reported as a pleural tumor but now has been defined as a tumor that can be seen everywhere in the human body. Histopathologically, many of the fibroblastic tumors can mimic SFT, and immunohistochemistry is necessary for differential diagnosis. Several markers have been used, and recently, STAT6 has been introduced as a diagnostic marker. No research study has been reported from Iran.

Objectives: In this report, we are trying to introduce our experience about the clinicopathologic findings of 35 cases of SFT during the last 10 years from our center with an emphasis on the diagnostic role of STAT6 in this tumor.

Patients and methods: During the last 10 years, we confirmed the diagnosis of 35 cases of SFT in the pathology archives of Shiraz University of Medical Sciences. These 35 cases were considered as cases. All the clinicopathologic findings were also extracted from the clinical charts of the patients. To evaluate the diagnostic role of STAT6, another 35 cases of spindle cell tumors were also extracted from the pathology archives as mimickers of SFT. STAT6 was stained in all of the 70 cases and controls.

Results and discussion: Our experience showed that SFT is more common in middle-aged men with a wide age range, although it is very rare in children. It can be present in every location with a wide size range from less than 1 cm to more than 15 cm. The presence of abnormal staghorn vessels is one of the main diagnostic histopathologic characteristics. STAT6 showed a sensitivity and specificity of 91% and 86% in the diagnosis of SFT. Other markers such as CD99, CD34, and BCL2 have also been considered useful in the differential diagnosis of this tumor, although the diagnostic accuracy seems to be lower than STAT6. High mitosis, presence of necrosis, and atypia are important criteria for predicting malignant and aggressive behavior in SFT. Among 35 cases in our study, 17% showed malignant behavior as recurrent or metastatic tumors.

Conclusion: Solitary fibrous tumor is a common soft tissue tumor that can be seen everywhere and needs careful histopathologic and immunohistochemical evaluation for the correct diagnosis and prediction of aggressive or benign behavior.

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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
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7.70%
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