StayCurrentMD · Diagnostic and prognostic utility of SF1, IGF2 and p57 immunoexpression in pediatric adrenal cortical tumors
Article1 min read·Published Jan 2019Older

Diagnostic and prognostic utility of SF1, IGF2 and p57 immunoexpression in pediatric adrenal cortical tumors

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Article · Jan 2019 · 1 min read

In brief

In brief

Study of 25 pediatric adrenocortical tumors demonstrates that SF-1 and IGF2 immunostaining, combined with Ki67 labeling index, provides reliable diagnostic and prognostic assessment when using Weineke criteria. Increased expression of these markers correlates with malignancy and worse survival, while p57 helps identify benign tumors.

Written by the GCMD Library team from the article.

Abstract

Background

Adrenocortical tumors (ACT) are uncommon in the pediatric age group. Using the standard Weiss criteria in pediatric tumors leads to overdiagnosis. This has led to the development of newer systems such as Weineke criteria. Ki67 labeling index aids in differentiating adenomas from carcinomas. We aim to evaluate the diagnostic and prognostic role of Ki67 labeling index, along with immunoexpression of steroidogenic factor-1, insulin like growth factor 2 and p57, in pediatric ACTs diagnosed using Weineke criteria.

Methods

We have studied 25 cases of pediatric ACTs. Immunohistochemical staining for Ki67, SF-1, IGF2 and p57 was done in all cases and the result was correlated with the morphological diagnosis using the Weineke criteria.

Results

Ki67 labeling index showed complete concordance with the morphological diagnosis. SF-1 and IGF2 showed similar correlation with the diagnosis, with IGF-2 proving to be a more specific marker. Increased Ki67, SF-1 and IGF2 immunostaining also correlated with worse survival. p57 was more specific in determining benign status of a tumor.

Conclusion

SF-1 and IGF2 are highly sensitive markers of malignancy in pediatric ACTs and can be used in combination with Ki67 expression for optimal diagnostic and prognostic assessment of pediatric ACTs.

Type of study

Prognosis study.

Level of evidence

Level II.

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