Diagnostic value of immunohistochemistry and FISH for chromosome 12p in type Ⅱ testicular germ cell tumors.
- Author:
Qin SHEN
1
;
Qiu RAO
1
;
Bo YU
1
;
Qiu-Yuan XIA
1
;
Wei BAO
1
;
Zhen-Feng LU
1
;
Qun-Li SHI
1
;
Xiao-Jun ZHOU
1
Author Information
- Publication Type:Journal Article
- Keywords: fluorescence in situ hybridization; immunohistochemistry; isochromosome of chromosome 12p; testicular germ cell tumor, type Ⅱ; testis
- MeSH: Biomarkers, Tumor; metabolism; Carcinoma, Embryonal; diagnosis; genetics; metabolism; pathology; Chromosome Aberrations; Chromosomes, Human, Pair 12; Endodermal Sinus Tumor; diagnosis; genetics; metabolism; pathology; Genetic Markers; Humans; Immunohistochemistry; In Situ Hybridization, Fluorescence; Male; Neoplasms, Germ Cell and Embryonal; diagnosis; genetics; metabolism; pathology; Prognosis; Seminiferous Tubules; metabolism; Seminoma; diagnosis; genetics; metabolism; pathology; Teratoma; diagnosis; genetics; metabolism; pathology; Testicular Neoplasms; diagnosis; genetics; metabolism; pathology
- From: National Journal of Andrology 2016;22(8):692-697
- CountryChina
- Language:Chinese
-
Abstract:
ObjectiveTo study the pathological morphology, immunohistochemical characteristics, and molecular changes of type Ⅱ testicular germ cell tumors (TGCT) and investigate the possible value of immunohistochemistry and fluorescence in situ hybridization (FISH) in the diagnosis of TGCT.
METHODSWe collected for this study 97 cases of TGCT, including 75 cases of seminoma, 17 cases of embryonal carcinoma, 11 cases of yolk sac tumor, 16 cases of mature teratoma, 3 cases of immature teratoma, and 1 case of epidermoid cyst, in which normal testicular tissue was found in 20 and non-TGCT in 6. We detected the expressions of different antibodies in various subtypes of TGCT by immunohistochemistry and determined the rate of chromosome 12p abnormality using FISH.
RESULTSThe immunophenotypes varied with different subtypes of TGCT. SALL4 and PLAP exhibited high sensitivity in all histological subtypes. CD117 and OCT4 showed strongly positive expressions in invasive seminoma and germ cell neoplasia in situ (GCNIS) but not in normal seminiferous tubules. GPC3 was significantly expressed in the yolk sac tumor, superior to GATA3 and AFP in both range and intensity. CKpan, OCT4, and CD30 were extensively expressed in embryonal carcinoma, while HCG expressed in choriocarcinoma. The positivity rate of isochromosome 12p and 12p amplification in TGCT was 96.7% (29/30).
CONCLUSIONSThe majority of TGCT can be diagnosed by histological observation, but immunohistochemical staining is crucial for more accurate subtypes and valuable for selection of individualized treatment options and evaluation of prognosis. Chromosome 12p abnormality is a specific molecular alteration in type Ⅱ TGCT, which is useful for ruling out other lesions.
