Thymic tumours in Denmark. A retrospective study of 213 cases from 1970-1993

Pathol Res Pract. 1999;195(8):565-70. doi: 10.1016/S0344-0338(99)80006-5.

Abstract

Histological slides of 213 thymic tumours were reviewed twice and classified according to Kirchner and Müller-Hermelink into 122 thymomas (syn. organotypic thymic epithelial tumours (TET)), 58 thymic carcinomas (syn. non-organotypic TET) and 16 lymphomas. Tumour heterogeneity (i.e. features of two subtypes in one tumour) appeared in 38% of the organotypic TET. The overall diagnostic correspondence between the reviews of the 122 organotypic TET was 48%. By reducing the five diagnostic groups to three: organotypic TET benign (medullary and mixed thymomas), organotypic TET low-grade (organoid and cortical thymomas and well-differentiated thymic carcinoma (WDTC)) and non-organotypic TET (usually high-grade thymic carcinomas), and minimising the effect of tumour heterogeneity in this way, the diagnostic correspondence increased to 82%. Correlating histological type with stage, we found that 80% of medullary and 87% of mixed thymomas were stage I, that 85% of cortical and 81% of WDTC were stage II or III, and that non-organotypic TET were stage II or III (86%) or stage IV (14%), respectively. It is suggested to report on the heterogeneity of a given case of thymic epithelial tumour in the pathology reports and give the approximate percentage of each component, telling the clinician which component may determine the prognosis.

MeSH terms

  • Cysts / classification
  • Cysts / pathology*
  • Denmark
  • Humans
  • Lymphoma / classification
  • Lymphoma / pathology*
  • Neoplasm Staging
  • Retrospective Studies
  • Thymoma / classification
  • Thymoma / pathology*
  • Thymus Neoplasms / classification
  • Thymus Neoplasms / pathology*