Clinical Impact of the Current WHO Classification of Pituitary Adenomas
- PMID: 26860936
- DOI: 10.1007/s12022-016-9418-7
Clinical Impact of the Current WHO Classification of Pituitary Adenomas
Abstract
WHO classifications should be used for comparing the results from different groups of pathologist and clinicians by standardized histopathological methods. Our present report describes the important parameters of pituitary adenoma pathology as demand of the WHO classification for correlation to endocrine data and prognosis. The combination of HE stain based structures with immunostainings for pituitary hormones allows subclassification of adenomas as the best method not only for correlations to clinical hyperfunctions but also for statements to the sensitivity of drug therapies (somatostatin analogs, dopamine agonists). GH-, PRL- and ACTH-secreting pituitary adenomas are further classified based on the size and number of their secretory granules by electron microscopy, or as is mostly the case nowadays by cytokeratin staining pattern, into densely and sparsely granulated. Granulation pattern may be considered for the prediction of treatment response in patients with GH-secreting adenomas, since the sparsely granulated subtype was shown to be less responsive to somatostatin analog treatment. For prognosis, it is important to identify aggressive adenomas by measurements of the Ki-67 index, of the number of mitoses, and of nuclear expression of p53. Among the criteria for atypical adenomas, high Ki-67 labeling index and invasive character are the most important adverse prognostic factors. Promising molecular markers have been identified that might supplement the currently used proliferation parameters. For defining atypical adenomas in a future histopathological classification system, we propose to provide the proliferative potential and the invasive character separately.
Keywords: Adenoma; Classification; Clinical impact; Pituitary; WHO.
Similar articles
-
Pathohistological classification of pituitary tumors: 10 years of experience with the German Pituitary Tumor Registry.Eur J Endocrinol. 2007 Feb;156(2):203-16. doi: 10.1530/eje.1.02326. Eur J Endocrinol. 2007. PMID: 17287410 Review.
-
Subclinical adenomas in postmortem pituitaries: classification and correlations to clinical data.Eur J Endocrinol. 2006 May;154(5):753-8. doi: 10.1530/eje.1.02107. Eur J Endocrinol. 2006. PMID: 16645024
-
Emerging Histopathological and Genetic Parameters of Pituitary Adenomas: Clinical Impact and Recommendation for Future WHO Classification.Endocr Pathol. 2016 Jun;27(2):115-22. doi: 10.1007/s12022-016-9419-6. Endocr Pathol. 2016. PMID: 26874696 Review.
-
Clinical Implications of the New WHO Classification 2017 for Pituitary Tumors.Exp Clin Endocrinol Diabetes. 2021 Mar;129(3):146-156. doi: 10.1055/a-1310-7900. Epub 2021 Mar 9. Exp Clin Endocrinol Diabetes. 2021. PMID: 33690870 Review.
-
New WHO classification of pituitary adenomas (4th edition): assessment of pituitary transcription factors and the prognostic histological factors.Brain Tumor Pathol. 2018 Apr;35(2):57-61. doi: 10.1007/s10014-017-0307-7. Epub 2018 Jan 9. Brain Tumor Pathol. 2018. PMID: 29318396 Review.
Cited by
-
Expression of programmed death-ligand 1 (PD-L1) in human pituitary neuroendocrine tumor.Cancer Immunol Immunother. 2020 Oct;69(10):2053-2061. doi: 10.1007/s00262-020-02611-x. Epub 2020 May 22. Cancer Immunol Immunother. 2020. PMID: 32445029 Free PMC article.
-
Clinicopathological significance of baseline T2-weighted signal intensity in functional pituitary adenomas.Pituitary. 2018 Aug;21(4):347-354. doi: 10.1007/s11102-018-0877-3. Pituitary. 2018. PMID: 29460202
-
Aggressive somatotrophinomas lacking clinical symptoms: neurosurgical management.Neurosurg Rev. 2018 Oct;41(4):999-1005. doi: 10.1007/s10143-017-0940-y. Epub 2017 Dec 30. Neurosurg Rev. 2018. PMID: 29290044
-
Prolactinomas in males: any differences?Pituitary. 2020 Feb;23(1):52-57. doi: 10.1007/s11102-019-01009-y. Pituitary. 2020. PMID: 31802331 Review.
-
Pediatric Pituitary Adenoma: Case Series, Review of the Literature, and a Skull Base Treatment Paradigm.J Neurol Surg B Skull Base. 2018 Feb;79(1):91-114. doi: 10.1055/s-0038-1625984. Epub 2018 Jan 24. J Neurol Surg B Skull Base. 2018. PMID: 29404245 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous