Testicular Seminoma: A Clinicopathologic and Immunohistochemical Study of 105 Cases with Special Reference to Seminomas with Atypical Features
Open Access
- 1 January 2002
- journal article
- research article
- Published by SAGE Publications in International Journal of Surgical Pathology
- Vol. 10 (1) , 23-32
- https://doi.org/10.1177/106689690201000105
Abstract
In spite of the high curability rates, rare cases of testicular seminoma behave in an unexpectedly aggressive manner. No effective markers are currently available that can predict such uncommon behavior. We studied 105 cases of testicular seminoma on whom the primary resection was performed at the Memorial Sloan-Kettering Cancer Center, New York, to investigate any relationship between morphology, im munohistochemical features, and clinical/pathological stages. Fifty-nine percent of the cases presented with pT stage 1 and 74 percent with American Joint Committee on Cancer (AJCC) stage I. In univariate analysis, tumor size, mitotic count, and pres ence of necrosis showed significant associations with pT stage (p = 0.0001, 0.0001, and 0.04, respectively), and the presence of vascular invasion (p = 0.0001, 0.0001, and 0.02, respectively). In multivariate analysis, both the tumor size and mitotic counts were independent predictors of pT stage (p = 0.0004 and 0.0001) and vascu lar invasion (p = 0.0004 and 0.0001). When tumors were separated on the basis of architectural and/or cytological atypia into 'usual seminomas' and 'seminomas with atypia,' these were significantly associated with AJCC stage (p = 0.02), and c-kit pro tein (p = 0.0005) and CD30 expression (p = 0.02). In addition, 'seminomas with atypia' also tended to show a higher proliferation activity as judged by Ki67 reactiv ity (p = 0.06), as well as express the marker of epithelial differentiation, Cam 5.2 (p = 0.09). In summary, we find that the morphologic features in testicular semi nomas are associated with factors of clinical relevance. Also, 'seminomas with atypia' differ from 'usual seminomas' morphologically, present at a higher AJCC stage, and possibly represent an early step in transformation of seminomas toward a more aggressive phenotype. While not proposing a new entity, we suggest that when these atypical features are encountered in an otherwise classical seminoma, investigations must be performed to exclude an early carcinomatous differentiation or even earlier changes toward such a differentiation, such as lack of c-kit protein expression. Int J Surg Pathol 10(1):23-32, 2002Keywords
This publication has 26 references indexed in Scilit:
- Activating c-kit Gene Mutations in Human Germ Cell TumorsThe American Journal of Pathology, 1999
- Testicular Germ-Cell CancerNew England Journal of Medicine, 1997
- CD30 expression in seminomaHuman Pathology, 1996
- Differential expression of the c‐kit proto‐oncogene in germ cell tumoursThe Journal of Pathology, 1995
- Expression of the c-kit Proto-Oncogene and Its Ligand Stem Cell Factor (SCF) in Normal and Malignant Human Testicular TissueJournal of Urology, 1995
- Preferential localization of c-kit product in tissue mast cells, basal cells of skin, epithelial cells of breast, small cell lung carcinoma and seminoma/dysgerminoma in human: immunohistochemical study on formalin-fixed, paraffin-embedded tissuesVirchows Archiv, 1994
- Classical and anaplastic seminoma: difference in survival.Radiology, 1988
- Mitosis counting in seminoma:An exercise of questionable significanceHuman Pathology, 1988
- Mitotic count in seminomas ? an unreliable criterion for distinguishing between classical and anaplastic typesVirchows Archiv, 1981
- Metastases from testicular carcinoma Study of 78 autopsied casesUrology, 1976