Skip to main content
Journal cover image

Demonstration of phenotypic abnormalities of thymic epithelium in thymoma including two cases with abundant Langerhans cells.

Publication ,  Journal Article
Kraus, VB; Harden, EA; Wittels, B; Moore, JO; Haynes, BF
Published in: Am J Pathol
September 1988

A panel of monoclonal antibodies that phenotypically define stages of normal human thymic epithelial (TE) cell maturation was used to compare thymic epithelium of nine thymomas with hyperplastic thymic epithelium in myasthenia gravis (MG) and thymic epithelium of normal thymuses. It has been shown previously that normal thymic epithelial cells express antigens of early TE cell maturation (A2B5, TE-4) throughout thymic ontogeny and acquire antigens 12/1-2, TE8, and TE-15 at 14 to 16 weeks of fetal gestation. Hyperplastic MG thymic epithelial cells expressed TE antigens in phenotypic patterns similar to that seen in normal postnatal thymus, ie, TE in subcapsular cortex and medulla was TE4+, A2B5+, and 12/1 - 2+ and Hassall's bodies were reactive with antibodies TE8 and TE15. In contrast, thymic epithelium in primary mediastinal thymomas was TE4+, A2B5+, TE8-, and greater than 75% of thymoma epithelium was 12/1 - 2-, a thymic epithelial phenotype similar to that seen on normal fetal thymic epithelium at 14 to 16 weeks fetal gestation. In one subject with a mature epithelial histologic pattern, thymoma epithelium was found to be strongly TE8+, a phenotype suggestive of a later stage of TE maturation. Lymphocytes in five of seven thymomas with immature thymic epithelial cells predominantly expressed immature thymocyte phenotype while two thymomas with immature epithelial phenotype showed a predominance of Langerhans cells and surrounding lymphocytes expressing a mature phenotype. Lymphocytes in the thymoma with differentiated epithelial cells expressed a mature thymocyte phenotype. Thus, in thymomas of varying histologic types, phenotypic abnormalities of thymic epithelium are present; these phenotypic abnormalities may reflect abnormal thymic epithelial maturation.

Duke Scholars

Published In

Am J Pathol

ISSN

0002-9440

Publication Date

September 1988

Volume

132

Issue

3

Start / End Page

552 / 562

Location

United States

Related Subject Headings

  • Thymus Neoplasms
  • Thymoma
  • Phenotype
  • Pathology
  • Myasthenia Gravis
  • Middle Aged
  • Male
  • Langerhans Cells
  • Humans
  • Female
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Kraus, V. B., Harden, E. A., Wittels, B., Moore, J. O., & Haynes, B. F. (1988). Demonstration of phenotypic abnormalities of thymic epithelium in thymoma including two cases with abundant Langerhans cells. Am J Pathol, 132(3), 552–562.
Kraus, V. B., E. A. Harden, B. Wittels, J. O. Moore, and B. F. Haynes. “Demonstration of phenotypic abnormalities of thymic epithelium in thymoma including two cases with abundant Langerhans cells.Am J Pathol 132, no. 3 (September 1988): 552–62.
Kraus VB, Harden EA, Wittels B, Moore JO, Haynes BF. Demonstration of phenotypic abnormalities of thymic epithelium in thymoma including two cases with abundant Langerhans cells. Am J Pathol. 1988 Sep;132(3):552–62.
Kraus VB, Harden EA, Wittels B, Moore JO, Haynes BF. Demonstration of phenotypic abnormalities of thymic epithelium in thymoma including two cases with abundant Langerhans cells. Am J Pathol. 1988 Sep;132(3):552–562.
Journal cover image

Published In

Am J Pathol

ISSN

0002-9440

Publication Date

September 1988

Volume

132

Issue

3

Start / End Page

552 / 562

Location

United States

Related Subject Headings

  • Thymus Neoplasms
  • Thymoma
  • Phenotype
  • Pathology
  • Myasthenia Gravis
  • Middle Aged
  • Male
  • Langerhans Cells
  • Humans
  • Female