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H-score of 11β-hydroxylase and aldosterone synthase in the histopathological diagnosis of adrenocortical tumors.

Authors :
Yang Y
Xiao M
Song Y
Tang Y
Luo T
Yang S
He W
Cheng Q
Ma L
Zhang Y
He Y
Cao Y
Yang J
Peng B
Hu J
Li Q
Source :
Endocrine [Endocrine] 2019 Sep; Vol. 65 (3), pp. 683-691. Date of Electronic Publication: 2019 Jul 22.
Publication Year :
2019

Abstract

Purpose: To assess the diagnostic performance of the H-score of 11β-hydroxylase (CYP11B1) and aldosterone synthase (CYP11B2) in the histopathological diagnosis of adrenocortical tumors (ACT).<br />Methods: We retrospectively evaluated 199 cases of ACT, of which 85 were diagnosed as aldosterone-producing adenoma (APA), 66 as cortisol-producing adenoma (CPA), 9 as aldosterone-cortisol co-secreting adenoma, 30 as nonhyperfunctioning adenoma, and 9 as adrenocortical carcinoma (ACC). Immunohistochemical staining was performed using anti-CYP11B1 and anti-CYP11B2 monoclonal antibodies. The staining was quantified by the McCarty's H-score system. The diagnostic performance was assessed by the receiver operating characteristic curve (ROC).<br />Results: The H-score of CYP11B1 is highest in the CPA group and lowest in the ACC group. The H-score of CYP11B2 in the APA group is significantly higher than other ACT groups. The area under ROC (AUC) of an increased H-score of CYP11B2 (>65) for the diagnosis of APA was 0.971 (95%CI 0.937-0.990). The AUC of an increased H-score of CYP11B1 (>204) for the diagnosis of CPA was 0.725 (95%CI 0.658-0.786). The AUC of a decreased H-score of CYP11B1 (<85) for the diagnosis of ACC was 0.960 (95%CI 0.923-0.983).<br />Conclusions: H-score of CYP11B1 and CYP11B2 are reliable tools for the histopathological subtyping of functional benign ACT and may offer some value in the histopathological diagnosis of malignant ACT.

Details

Language :
English
ISSN :
1559-0100
Volume :
65
Issue :
3
Database :
MEDLINE
Journal :
Endocrine
Publication Type :
Academic Journal
Accession number :
31332713
Full Text :
https://doi.org/10.1007/s12020-019-02022-8