肾及肾门孤立性纤维性肿瘤:43例临床病理分析。

IF 3.1 3区 医学 Q1 PATHOLOGY
Güneş Güner, Mahmut Akgul, Michael Michal, Asli Yilmaz, Buşra Yaprak Bayrak, Bermal Hasbay, Aylin Yazgan, Nilüfer Kandemir, Murat Oktay, Deniz Bayçelebi, Arkar Htoo, Jose Lopez, Ondrej Hes, Arndt Hartmann, Dilek E Baydar, Kril Trpkov, Sambit K Mohanty, Abbas Agaimy, Pedram Argani, Kemal Kösemehmetoğlu
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引用次数: 0

摘要

孤立性纤维性肿瘤(SFT)是一种纤维母细胞肿瘤,其特征是突出的、鹿角状或微妙的“血管外皮细胞瘤(HPC)样血管”,NAB2::STAT6基因融合及其替代STAT6表达。SFT可能表现出不可预测的临床病程,需要根据肿瘤特征进行风险评估。肾脏SFTs是罕见的,并没有很好的特征。我们回顾了43例原发性肾脏SFT病例的临床、形态学和免疫组织化学(STAT6、BCL2、CD34和PAX8)特征。基于患者年龄、肿瘤大小、有丝分裂活性和肿瘤坏死,采用Demicco的四变量风险分层。平均年龄49岁(11 ~ 83岁),女性略占优势(男女比例为20:23)。平均肿瘤大小为7.8 cm (1.6 ~ 32 cm)。肿瘤主要位于门部(22/ 32,68%),边界清晰(31/ 42,74%)。形态学上,肿瘤为1)纤维状(“sft样”,19/43,44%),以细胞密度低和突出的细网状或瘢痕状胶原为特征;2)细胞(“hpc样”,8/43,19%),具有高细胞性,短梭形到小细胞样增生,缺乏胶原背景;3)纤维/细胞混合(16/43,37%)显示两种成分。4例有脂肪瘤成分。BCL2阳性(28/28),CD34阳性(3例除外)(93%),STAT6阳性(1例除外)(39/40,97.5%)。6/34例(18%)患者PAX8阳性。大多数病例(29/ 43,68%)为低危组,其次为中度组(12/ 43,27%)和高危组(2/ 43,5%)。29例患者中有5例(18%)有转移性疾病,2例高风险和1例中危肿瘤患者死于该疾病,而25例低危或中危肿瘤患者平均存活约36个月。我们强调风险分层系统在预测预后方面的有用性。PAX8在肾SFT亚群中的表达是一个潜在的诊断缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Solitary fibrous tumor of kidney and renal hilus: a multi-institutional clinicopathologic analysis of 43 cases.

Solitary fibrous tumor (SFT) is a fibroblastic neoplasm characterized by prominent, staghorn, or delicate "hemangiopericytoma (HPC)-like vasculature", NAB2::STAT6 gene fusion, and its surrogate STAT6 expression. SFT may exhibit an unpredictable clinical course, necessitating risk assessment based on tumor characteristics. Renal SFTs are rare and have not been well characterized. Forty-three primary kidney SFT cases are reviewed for clinical, morphological, and immunohistochemical (STAT6, BCL2, CD34, and PAX8) features. A four-variable risk stratification by Demicco was applied based on patient age, tumor size, mitotic activity, and tumor necrosis. The mean age was 49 years (range 11-83 years) with a slight female predominance (male:female = 20:23). The mean tumor size was 7.8 cm (1.6-32 cm). Tumors were mainly located at the hilus (22/32, 68%) and had well-demarcated borders (31/42, 74%). Morphologically, tumors were categorized as 1) Fibrous ("SFT-like", 19/43, 44%), characterized by hypocellularity and prominent fine-reticular or keloidal collagen; 2) Cellular ("HPC-like", 8/43, 19%), with hypercellularity, short spindle to small cell-like proliferation, and lacking a collagenous background; 3) mixed fibrous/cellular (16/43, 37%) displaying both components. Four cases featured a lipomatous component. BCL2 was positive in all tested cases (28/28), CD34 in all but 3 cases (93%), and STAT6 in all but one case (39/40, 97.5%). PAX8 was positive in 6/34 (18%) cases. Most cases (29/43, 68%) were classified as low-risk, followed by intermediate (12/43, 27%) and high-risk (2/43, 5%) groups. Five of 29 (18%) patients had metastatic disease, and two patients with high-risk and one with intermediate-risk tumors died from the disease, while 25 patients with low- or intermediate-risk tumors were alive for an average of about 36 months. We emphasize the usefulness of the risk stratification system in predicting prognosis. PAX8 expression in a subset of renal SFT represents a potential diagnostic pitfall.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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