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非典型和恶性血管球瘤:52例分析,并对血管球瘤重新分类提出建议。

Atypical and malignant glomus tumors: analysis of 52 cases, with a proposal for the reclassification of glomus tumors.

作者信息

Folpe A L, Fanburg-Smith J C, Miettinen M, Weiss S W

机构信息

Department of Pathology and Laboratory Medicine, Emory University, Atlanta, Georgia 30322, USA.

出版信息

Am J Surg Pathol. 2001 Jan;25(1):1-12. doi: 10.1097/00000478-200101000-00001.

Abstract

Occasional glomus tumors display unusual features, such as large size, deep location, infiltrative growth, mitotic activity, nuclear pleomorphism, and necrosis. Although a small number of purportedly malignant glomus tumors have been described, histologic criteria for malignancy in glomus tumors have never been elaborated. The authors studied 52 unusual glomus tumors (retrieved from their consultation files) previously diagnosed as "atypical" or "malignant" by virtue of nuclear atypia, infiltrative growth, or mitotic activity. They evaluated size, depth, growth pattern, cellularity, nuclear grade, number of mitotic figures per 50 high-power fields (HPF), atypical mitotic figures, vascular space involvement, and necrosis to define criteria for malignancy in glomus tumors. Estimated relative risk was calculated and the Fisher exact test was used for statistical analysis. The 27 female patients and the 25 male patients ranged in age from 8 to 83 years (median age, 43 years). The tumors measured from 0.2 to 12 cm (median size, 2 cm) and occurred predominantly in the extremities, in both the superficial (n = 35) and deep (n = 17) soft tissues. Atypical features were usually observed centrally with a rim of benign-appearing glomus tumor. Follow-up information (n = 35; range, 5 months-23 years; mean 5.5 years) showed seven recurrences, eight metastases, and seven deaths from disease. Five-year cumulative metastatic risk increased significantly for tumors with a deep location (p = 0.005), with a size of more than 2 cm (p = 0.004), and with atypical mitotic figures (p = 0.004). Mitotic activity of more than 5 mitoses/50 HPF, high cellularity, the presence of necrosis, and moderate to high nuclear grade approached but did not reach significance. High nuclear grade alone, infiltrative growth, and vascular space involvement were not associated with metastasis. The authors propose the following classification scheme and criteria. Malignant glomus tumor: Tumors with a deep location and a size of more than 2 cm, or atypical mitotic figures, or moderate to high nuclear grade and > or =5 mitotic figures/50 HPF. Symplastic glomus tumor: Tumors with high nuclear grade in the absence of any other malignant feature. Glomus tumor of uncertain malignant potential: Tumors that lack criteria for malignant glomus tumor or symplastic glomus tumor but have high mitotic activity and superficial location only, or large size only, or deep location only. Glomangiomatosis: Tumors with histologic features of diffuse angiomatosis and excess glomus cells. Using this classification scheme, metastasis was observed in 38% of tumors fulfilling the criteria for malignancy. In contrast, metastatic disease was not seen in any specimen classified as symplastic glomus tumor, glomus tumor of uncertain malignant potential, or glomangiomatosis.

摘要

偶见的血管球瘤表现出不寻常的特征,如体积大、位置深、浸润性生长、有丝分裂活性、核多形性和坏死。尽管已有少数所谓恶性血管球瘤的报道,但血管球瘤恶性的组织学标准从未得到阐述。作者研究了52例不寻常的血管球瘤(从会诊档案中检索),这些肿瘤先前因核异型性、浸润性生长或有丝分裂活性而被诊断为“非典型”或“恶性”。他们评估了肿瘤的大小、深度、生长方式、细胞密度、核分级、每50个高倍视野(HPF)中的有丝分裂象数量、非典型有丝分裂象、血管腔受累情况和坏死情况,以确定血管球瘤恶性的标准。计算估计相对风险,并使用Fisher精确检验进行统计分析。27例女性患者和25例男性患者年龄范围为8至83岁(中位年龄43岁)。肿瘤大小为0.2至12 cm(中位大小2 cm),主要发生在四肢的浅表(n = 35)和深部(n = 17)软组织中。非典型特征通常在中央观察到,周围有外观良性的血管球瘤边缘。随访信息(n = 35;范围5个月至23年;平均5.5年)显示7例复发、8例转移和7例死于该疾病。对于位置深(p = 0.005)、大小超过2 cm(p = 0.004)和有非典型有丝分裂象(p = 0.004)的肿瘤,5年累积转移风险显著增加。每50 HPF有丝分裂活性超过5个有丝分裂象、细胞密度高、存在坏死以及中度至高度核分级接近但未达到统计学意义。单独的高度核分级、浸润性生长和血管腔受累与转移无关。作者提出了以下分类方案和标准。恶性血管球瘤:位置深且大小超过2 cm,或有非典型有丝分裂象,或中度至高度核分级且每50 HPF有丝分裂象≥5个的肿瘤。合体细胞性血管球瘤:无任何其他恶性特征但核分级高的肿瘤。恶性潜能不确定的血管球瘤:缺乏恶性血管球瘤或合体细胞性血管球瘤标准,但仅具有高有丝分裂活性和浅表位置,或仅具有大体积,或仅具有深部位置的肿瘤。弥漫性血管瘤病:具有弥漫性血管瘤病组织学特征且血管球细胞过多的肿瘤。使用该分类方案,在符合恶性标准的肿瘤中有38%观察到转移。相比之下,在分类为合体细胞性血管球瘤、恶性潜能不确定的血管球瘤或弥漫性血管瘤病的任何标本中均未见到转移性疾病。

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