Clinical and functional significance of WHO classification on human thymic epithelial neoplasms - A study of 146 consecutive tumors

被引:128
作者
Okumura, M
Miyoshi, S
Fujii, Y
Takeuchi, Y
Shiono, H
Inoue, M
Fukuhara, K
Kadota, Y
Tateyama, H
Eimoto, T
Matsuda, H
机构
[1] Osaka Univ, Grad Sch Med, Dept Surg E1, Div Gen Thorac Surg, Suita, Osaka 5650871, Japan
[2] Nagoya City Univ, Sch Med, Dept Surg, Nagoya, Aichi 467, Japan
[3] Nagoya City Univ, Sch Med, Dept Pathol 2, Nagoya, Aichi, Japan
关键词
thymus; thymoma; thymic carcinama; Myasthenia gravis; CD4(+)CD8(+) cells;
D O I
10.1097/00000478-200101000-00012
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We examined the clinical and functional significance of histologic classification of thymic epithelial neoplasms proposed by the World Health Organization (WHO), based on an analysis of 146 consecutive tumors derived from 141 patients and 47 normal thymuses derived from children ranging in age from 1 to 9 years. Invasive tumors were seen in 12.5%, 38.6%, 40.0%, 69.4%, 80.0%, and 100% of type A, AB, B1, B2, B3, and C primary tumors, respectively. All of six recurrent or metastatic lesions were type B2 tumors. Myasthenia gravis was associated in 0%, 6.8%, 40.0%, 55.6%, 10.0%, and 0% in patients with type A, AB, B1, B2, B3, and C tumors, respectively. The average number (x10(6)) of tumor-associated CD4(+)CD8(+) cells present in 1 g of tumor tissue was 1.5, 391.1, 1041.7, 333.9, 24.5, and 0.2 in type A, AB, BI, B2, B3, and C, respectively, and it was 1168.2 in the normal thymuses. Thus, type B1 tumor retained the function to induce CD4+CD8+ double-positive cells at a level comparable to that of the normal thymic cortical epithelial cells, followed by type AB and type B2 tumors. Type A and B3 tumors had this function at a barely detectable level, and type C tumor was nonfunctional. WHO histologic classification was shown to reflect the clinical features and the T-cell-inducing function of thymic epithelial tumors.
引用
收藏
页码:103 / 110
页数:8
相关论文
共 36 条
[1]   THE PREDOMINANT LYMPHOCYTE IN MOST THYMOMAS AND IN NONNEOPLASTIC THYMUS FROM PATIENTS WITH MYASTHENIA-GRAVIS IS THE CORTICAL THYMOCYTE [J].
AISENBERG, AC ;
WILKES, B ;
HARRIS, NL ;
FRIST, WH .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1985, 35 (01) :130-136
[2]  
[Anonymous], 1997, ATLAS TUMOR PATHOL
[3]  
[Anonymous], 1976, ATLAS TUMOR PATHOLOG
[4]  
BERNATZ PE, 1961, J THORAC CARDIOV SUR, V42, P424
[5]   THYMUS-CELLS IN MYASTHENIA-GRAVIS - A 2-COLOR FLOW CYTOMETRIC ANALYSIS OF LYMPHOCYTES IN THE THYMUS AND THYMOMA [J].
FUJII, Y ;
HAYAKAWA, M ;
NAKAHARA, K .
JOURNAL OF NEUROLOGY, 1992, 239 (02) :82-88
[6]   Flow cytometric study of lymphocytes associated with thymoma and other thymic tumors [J].
Fujii, Y ;
Okumura, M ;
Yamamoto, S .
JOURNAL OF SURGICAL RESEARCH, 1999, 82 (02) :312-318
[7]   LYMPHOCYTES IN THYMOMA - ASSOCIATION WITH MYASTHENIA-GRAVIS IS CORRELATED WITH INCREASED NUMBER OF SINGLE-POSITIVE CELLS [J].
FUJII, Y ;
HAYAKAWA, M ;
INADA, K ;
NAKAHARA, K .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (10) :2355-2358
[8]  
Harris NL, 1999, AM J CLIN PATHOL, V112, P299
[9]   PE-35-related antigen expression and CD1a-positive lymphocytes in thymoma subtypes based on Muller-Hermelink classification - An immunohistochemical study using catalyzed signal amplification [J].
Hattori, H ;
Tateyama, H ;
Tada, T ;
Saito, Y ;
Yamakawa, Y ;
Eimoto, T .
VIRCHOWS ARCHIV, 2000, 436 (01) :20-27
[10]  
Inoue M, 1998, CLIN EXP IMMUNOL, V112, P419