Key result
IGFII expression was detected in 13 of 17 adrenocortical carcinomas compared to 1 of 22 adenomas, and a MIB1 index >5% was found in 14 of 16 carcinomas versus 1 of 22 adenomas.
Why the study?
Does immunohistochemical evaluation of IGFII and MIB1 improve the differentiation of benign from malignant adrenocortical tumours?
Observational (n=39)
Does immunohistochemical evaluation of IGFII and MIB1 improve the differentiation of benign from malignant adrenocortical tumours?
IGFII and MIB1 immunohistochemistry provides high sensitivity and specificity for differentiating malignant from benign adrenocortical tumours.
May support IGFII/MIB1 IHC for adrenocortical tumor differentiation; leaves open prospective validation before clinical adoption.
AIMS: The differentiation of adrenocortical carcinomas from adenomas may be difficult based on morphology alone. Differential expression of insulin-like growth factor (IGF) II and cyclin-dependent kinase (CDK) 4 has recently been described in these tumours. The aim of this study was to investigate the diagnostic usefulness of these markers immunohistochemically. METHODS AND RESULTS: We examined 22 benign and 17 malignant adrenocortical tumours and compared IGFII and CDK4 expression with known immunohistochemical as well as morphological criteria of malignancy. Thirteen of 17 carcinomas showed immunohistochemical reactivity for IGFII, whereas all adenomas but one were negative. Intense CDK4 expression was detected in 11 of 17 carcinomas but was present in only three of 22 adenomas. The MIB1 index was >5% in 14 of 16 carcinomas and was <5% in all adenomas but one. The combination of IGFII immunohistochemistry with MIB1 index led to high sensitivity and specificity in detecting adrenocortical carcinomas. CONCLUSIONS: IGFII and MIB1 are helpful immunohistochemical markers to predict malignancy in adrenocortical neoplasms. These markers can be used in addition to clinical, gross and morphological features to establish a diagnosis in difficult cases.
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Schmitt et al. (2006) conducted an observational in Adrenocortical tumours (n=39). IGFII, CDK4, and MIB1 immunohistochemistry vs. Benign adrenocortical adenomas was evaluated on Immunohistochemical reactivity for IGFII, CDK4, and MIB1 index. IGFII expression was detected in 13 of 17 adrenocortical carcinomas compared to 1 of 22 adenomas, and a MIB1 index >5% was found in 14 of 16 carcinomas versus 1 of 22 adenomas.
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