Atypical and malignant glomus tumors - Analysis of 52 cases, with a proposal for the reclassification of glomus tumors

被引:453
作者
Folpe, AL
Fanburg-Smith, JC
Miettinen, M
Weiss, SW
机构
[1] Emory Univ, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
[2] Armed Forces Inst Pathol, Dept Soft Tissue Pathol, Washington, DC 20306 USA
关键词
glomus tumor; glomangiosarcoma; angiomatosis; sarcoma;
D O I
10.1097/00000478-200101000-00001
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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 rumors 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 greater than or equal to5 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.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 34 条
[21]   GLOMANGIOSARCOMA OF THE LOWER-EXTREMITY [J].
NOER, H ;
KROGDAHL, A .
HISTOPATHOLOGY, 1991, 18 (04) :365-366
[22]  
Nuovo M, 1990, SURG PATHOL, V3, P31
[23]  
PORTER PL, 1991, MODERN PATHOL, V4, P46
[24]   Epithelioid smooth-muscle tumors of the uterus - A clinicopathologic study of 18 patients [J].
Prayson, RA ;
Goldblum, JR ;
Hart, WR .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1997, 21 (04) :383-391
[25]   EPITHELIOID GLOMUS TUMOR [J].
PULITZER, DR ;
MARTIN, PC ;
REED, RJ .
HUMAN PATHOLOGY, 1995, 26 (09) :1022-1027
[26]   ANGIOMATOSIS OF SOFT-TISSUE - AN ANALYSIS OF THE HISTOLOGIC FEATURES AND CLINICAL OUTCOME IN 51 CASES [J].
RAO, VK ;
WEISS, SW .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1992, 16 (08) :764-771
[27]   Cytokeratin 20: A marker for diagnosing Merkel cell carcinoma [J].
Scott, MP ;
Helm, KF .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1999, 21 (01) :16-20
[28]   EPITHELIOID LEIOMYOSARCOMA OF THE SKIN AND SUBCUTANEOUS TISSUE - CLINICOPATHOLOGICAL, IMMUNOHISTOCHEMICAL, AND ULTRASTRUCTURAL-STUDY OF 5 CASES [J].
SUSTER, S .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1994, 18 (03) :232-240
[29]  
WANG NP, 1995, AM J PATHOL, V147, P1799
[30]  
Watanabe K, 1995, Fukushima J Med Sci, V41, P71