Thymomas: clinical-pathological correlations

被引:0
作者
Lucchi, M
Basolo, F
Ribechini, A
Ambrogi, MC
Bencivelli, S
Fontaninj, G
Angeletti, CA
Mussi, A
机构
[1] Univ Pisa, Cardiac & Thorac Dept, Unit Thorac Surg, I-56124 Pisa, Italy
[2] Univ Pisa, Dept Oncol, Unit Pathol, I-56124 Pisa, Italy
关键词
thymoma; masaoka staging; surgery; WHO histological classification; follow-up; prognosis;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim. Since World Health organization (WHO) histologic typing of tumors of the thymus publication in 1999 only a few studies correlated this classification with the clinical features of the patients. We present the results of a retrospective analysis on patients, operated on for a thymoma, whose specimens were available, to compare the WHO thymoma histologic classification to the clinical behavior of the tumors. Methods. The specimens of 69 patients, who underwent surgical treatment between 1983 and 1998, were analyzed, comparing the clinical features of the patients and the hystological typing of the neoplasm, according to the WHO classification. A survival analysis of clinical and pathological prognostic factors was carried out. Results. The incidence of thymus-related syndrome was related to the histological subtype and increases progressively from A to B3, while in C subtype the incidence was nihl. With a mean follow-up of 108 months (range 54239 months), we experienced 6 intrathoracic recurrencies, 3 of those were intrapleuric and 3 mediastinal. At die last follow-up, 52 patients were alive; 1 with disease. Five deaths were related to the tumor (2 mediastinal and 3 intrapleuric relapses). Actuarial five-year and ten-year survival was 95% and 88.9%. Because of the absence of deaths related to thymomas in most samples it was not possible to perform a comparison among different histological types and different clinical stages. Conclusion. The WHO histologic classification seems to correlate with the incidence of thymus related syndromes and the clinical stage of Masaoka. Despite the higher incidence of recurrences in type B3 and C thymoma the WHO classification did not prove to be a prognostic factor.
引用
收藏
页码:89 / 93
页数:5
相关论文
共 25 条
[1]   TUMORS OF THYMUS AND THYMIC REGION .1. CLINICOPATHOLOGICAL STUDIES ON THYMOMAS [J].
BERGH, NP ;
GATZINSKY, P ;
LARSSON, S ;
LUNDIN, P ;
RIDELL, B .
ANNALS OF THORACIC SURGERY, 1978, 25 (02) :91-98
[2]   INVASIVE THYMOMA - THE ROLE OF MEDIASTINAL IRRADIATION FOLLOWING COMPLETE OR INCOMPLETE SURGICAL RESECTION [J].
CURRAN, WJ ;
KORNSTEIN, MJ ;
BROOKS, JJ ;
TURRISI, AT .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (11) :1722-1727
[3]   CHEMOTHERAPY OF INVASIVE THYMOMA [J].
FORNASIERO, A ;
DANIELE, O ;
GHIOTTO, C ;
SARTORI, F ;
REA, F ;
PIAZZA, M ;
FIOREDONATI, L ;
MORANDI, P ;
AVERSA, SML ;
PACCAGNELLA, A ;
PAPPAGALLO, GL ;
FIORENTINO, MV .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (08) :1419-1423
[4]   EXPERIENCE WITH SURGERY FOR THYMOMA ASSOCIATED WITH PURE RED BLOOD-CELL APLASIA - REPORT OF 3 CASES [J].
FUJIMURA, S ;
KONDO, T ;
YAMAUCHI, A ;
HANDA, M ;
NAKADA, T .
CHEST, 1985, 88 (02) :221-225
[5]   ADJUVANT RADIOTHERAPY AFTER COMPLETE RESECTION OF THYMOMA [J].
HANIUDA, M ;
MORIMOTO, M ;
NISHIMURA, H ;
KOBAYASHI, O ;
YAMANDA, T ;
IIDA, F .
ANNALS OF THORACIC SURGERY, 1992, 54 (02) :311-315
[6]   TREATMENT OF INVASIVE THYMOMA WITH PLEURAL DISSEMINATION [J].
ICHINOSE, Y ;
OHTA, M ;
YANO, T ;
YOKOYAMA, H ;
ASOH, H ;
HATA, K .
JOURNAL OF SURGICAL ONCOLOGY, 1993, 54 (03) :180-183
[7]   THYMIC HYPERPLASIA AND NEOPLASIA - REVIEW OF CURRENT CONCEPTS [J].
LEVINE, GD ;
ROSAI, J .
HUMAN PATHOLOGY, 1978, 9 (05) :495-515
[8]   CHEMOTHERAPY FOR ADVANCED THYMOMA - PRELIMINARY-RESULTS OF AN INTERGROUP STUDY [J].
LOEHRER, PJ ;
PEREZ, CA ;
ROTH, LM ;
GRECO, FA ;
LIVINGSTON, RB ;
EINHORN, LH .
ANNALS OF INTERNAL MEDICINE, 1990, 113 (07) :520-524
[9]   The multimodality treatment of thymic carcinoma [J].
Lucchi, M ;
Mussi, A ;
Basolo, F ;
Ambrogi, MC ;
Fontanini, G ;
Angeletti, CA .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2001, 19 (05) :566-569
[10]  
MACCHIARINI P, 1991, CANCER, V68, P706, DOI 10.1002/1097-0142(19910815)68:4<706::AID-CNCR2820680407>3.0.CO