Thymic hyperplasia is a rare cause of an anterior mediastinal mass in
children. True thymic hyperplasia is characterized by massive thymic h
ypertrophy with retention of normal thymic architecture, and must be d
istinguished from more commonly seen tumors of the anterior mediastinu
m. Previous reports of thymic hyperplasia primarily have been descript
ive, with minimal analysis of the cellular characteristics of the tumo
r. To better describe the cellular characteristics of thymic hyperplas
ia, the authors report on a 10-year-old boy found to have an asymptoma
tic 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 architectur
e. Because of the size and rapid growth of the mass, the authors decid
ed to resect it. Cellular analysis of the mass did not show difference
s from normal thymic elements. There was conserved thymic architecture
. The expression of cell surface markers and the proliferative respons
e of thymocytes to cytokines appeared to be normal. Similarly, a long
term cell culture of the thymocytes did not result in clonal prolifera
tion. Immunohistologic staining of stromal cell's showed no striking d
ifferences from normal thymic elements. Moreover, immunologic analysis
of the patient by standard hematological parameters, lymphocyte subse
ts, quantitative immunoglobins, and immunoelectrophoresis Showed no ab
normalities except for lymphocytosis, which resolved after tumor resec
tion. The authors conclude that thymic hyperplasia occurs in immunolog
ically normal children and may exhibit (1) rapid growth with minimal a
ssociated symptoms, (2) normal thymic architecture, (3) normal thymocy
te and stromal growth characteristics in vitro, and (4) a normal thymo
cyte response to cytokine stimulation. These data confirm, at a cellul
ar level, the clinical impression that thymic hyperplasia represents b
enign hypertrophy of the thymus rather than a thymic neoplasm.