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Massive thymic hyperplasia: characterization of a rare mediastinal mass.

Publication ,  Journal Article
Rice, HE; Flake, AW; Hori, T; Galy, A; Verhoogen, RH
Published in: J Pediatr Surg
December 1994

Thymic hyperplasia is a rare cause of an anterior mediastinal mass in children. True thymic hyperplasia is characterized by massive thymic hypertrophy with retention of normal thymic architecture, and must be distinguished from more commonly seen tumors of the anterior mediastinum. Previous reports of thymic hyperplasia primarily have been descriptive, with minimal analysis of the cellular characteristics of the tumor. To better describe the cellular characteristics of thymic hyperplasia, the authors report on a 10-year-old boy found to have an asymptomatic left paracardiac mass during cardiac evaluation. The mass enlarged rapidly during the following 2 weeks and filled the entire left side of the chest. An open biopsy specimen showed normal thymic architecture. Because of the size and rapid growth of the mass, the authors decided to resect it. Cellular analysis of the mass did not show differences from normal thymic elements. There was conserved thymic architecture. The expression of cell surface markers and the proliferative response of thymocytes to cytokines appeared to be normal. Similarly, a long-term cell culture of the thymocytes did not result in clonal proliferation. Immunohistologic staining of stromal cells showed no striking differences from normal thymic elements. Moreover, immunologic analysis of the patient by standard hematological parameters, lymphocyte subsets, quantitative immunoglobins, and immunoelectrophoresis showed no abnormalities except for lymphocytosis, which resolved after tumor resection. The authors conclude that thymic hyperplasia occurs in immunologically normal children and may exhibit (1) rapid growth with minimal associated symptoms, (2) normal thymic architecture, (3) normal thymocyte and stromal growth characteristics in vitro, and (4) a normal thymocyte response to cytokine stimulation.(ABSTRACT TRUNCATED AT 250 WORDS)

Duke Scholars

Published In

J Pediatr Surg

DOI

ISSN

0022-3468

Publication Date

December 1994

Volume

29

Issue

12

Start / End Page

1561 / 1564

Location

United States

Related Subject Headings

  • Thymus Gland
  • Radiography
  • Pediatrics
  • Mediastinum
  • Male
  • Hyperplasia
  • Humans
  • Child
  • 3213 Paediatrics
  • 3202 Clinical sciences
 

Citation

APA
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ICMJE
MLA
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Rice, H. E., Flake, A. W., Hori, T., Galy, A., & Verhoogen, R. H. (1994). Massive thymic hyperplasia: characterization of a rare mediastinal mass. J Pediatr Surg, 29(12), 1561–1564. https://doi.org/10.1016/0022-3468(94)90216-x
Rice, H. E., A. W. Flake, T. Hori, A. Galy, and R. H. Verhoogen. “Massive thymic hyperplasia: characterization of a rare mediastinal mass.J Pediatr Surg 29, no. 12 (December 1994): 1561–64. https://doi.org/10.1016/0022-3468(94)90216-x.
Rice HE, Flake AW, Hori T, Galy A, Verhoogen RH. Massive thymic hyperplasia: characterization of a rare mediastinal mass. J Pediatr Surg. 1994 Dec;29(12):1561–4.
Rice, H. E., et al. “Massive thymic hyperplasia: characterization of a rare mediastinal mass.J Pediatr Surg, vol. 29, no. 12, Dec. 1994, pp. 1561–64. Pubmed, doi:10.1016/0022-3468(94)90216-x.
Rice HE, Flake AW, Hori T, Galy A, Verhoogen RH. Massive thymic hyperplasia: characterization of a rare mediastinal mass. J Pediatr Surg. 1994 Dec;29(12):1561–1564.
Journal cover image

Published In

J Pediatr Surg

DOI

ISSN

0022-3468

Publication Date

December 1994

Volume

29

Issue

12

Start / End Page

1561 / 1564

Location

United States

Related Subject Headings

  • Thymus Gland
  • Radiography
  • Pediatrics
  • Mediastinum
  • Male
  • Hyperplasia
  • Humans
  • Child
  • 3213 Paediatrics
  • 3202 Clinical sciences