Neurol. praxi. 2024;25(4):267-273 | DOI: 10.36290/neu.2024.027

Update in diagnostic pathology of pituitary tumors - clinical and pathological perspective

MUDr. Jiří Soukup, Ph.D.1, 2, 3, MUDr. Mikuláš Kosák4, prof. MUDr. David Netuka, Ph.D.5, doc. MUDr. Filip Gabalec, Ph.D.6
1 Oddělení patologie, Ústřední vojenská nemocnice - Vojenská fakultní nemocnice Praha
2 Fingerlandův ústav patologie, Fakultní nemocnice Hradec Králové a Lékařská fakulta v Hradci Králové, Univerzita Karlova v Praze
3 Ústav patologie 1. lékařské fakulty Univerzity Karlovy a Všeobecné fakultní nemocnice, Praha
4 Interní klinika 1. LF UK a ÚVN, Ústřední vojenská nemocnice a Vojenská fakultní nemocnice Praha
5 Neurochirurgická a neuroonkologická klinika 1. LF UK a ÚVN v Praze
6 4. interní hematologická klinika, Fakultní nemocnice Hradec Králové a Lékařská fakulta v Hradci Králové, Univerzita Karlova v Praze

Pituitary tumors are common intracranial tumors in adults. Pituitary neuroendocrine tumors (PitNETs, formerly adenomas) represent a vast majority of pituitary lesions. These tumors can be classified according to the lineage of differentiation in tumor cells that corresponds to cellular subpopulations of normal pituitary. These cell lineages are determined by one or more transcription factors (Pit1, Tpit, SF1 and GATA3) that also regulate hormonal production in both normal pituitary cells and their neoplastic counterparts. This review article summarizes briefly current approach in histopathological diagnosis of PitNETs according to the latest WHO classification. Furthermore, rarer entities, including pituictyomas and craniopharyngiomas are discussed, as well as secondary tumors of sellar region.

Keywords: PitNETs, Pit1, Tpit, SF1, GATA3, pituicytoma, craniopharyngioma.

Received: January 19, 2024; Revised: April 16, 2024; Accepted: April 17, 2024; Prepublished online: April 17, 2024; Published: September 10, 2024  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Soukup J, Kosák M, Netuka D, Gabalec F. Update in diagnostic pathology of pituitary tumors - clinical and pathological perspective. Neurol. praxi. 2024;25(4):267-273. doi: 10.36290/neu.2024.027.
Download citation

References

  1. Al Argan R, Ramadhan A, Agnihotram RV, et al. Baseline MRI findings as predictors of hypopituitarism in patients with non­‑functioning pituitary adenomas. Endocr Connect. 2021;10(11):1445-1454. doi:10.1530/EC-21-0386. Go to original source... Go to PubMed...
  2. Apps JR, Muller HL, Hankinson TC, et al. Contemporary Biological Insights and Clinical Management of Craniopharyngioma. Endocr Rev. 2023;44(3):518-538. doi:10.1210/endrev/bnac035. Go to original source... Go to PubMed...
  3. Asa SL, Asioli S, Bozkurt S, et al. Pituitary neuroendocrine tumors (PitNETs): nomenclature evolution, not clinical revolution. Pituitary. 2019. doi:10.1007/s11102-019-01015-0. Go to original source... Go to PubMed...
  4. Asa SL, Casar­‑Borota O, Chanson P, et al.; attendees of 14th Meeting of the International Pituitary Pathology Club, A. F. N. From pituitary adenoma to pituitary neuroendocrine tumor (PitNET): an International Pituitary Pathology Club proposal. Endocr Relat Cancer. 2017;24(4):C5-C8. doi:10.1530/ERC-17-0004. Go to original source... Go to PubMed...
  5. Asa SL, Mete O, Perry A, et al. Overview of the 2022 WHO Classification of Pituitary Tumors. Endocr Pathol. 2022;33(1):6-26. doi:10.1007/s12022-022-09703-7. Go to original source... Go to PubMed...
  6. Asioli S, Righi A, Iommi M, et al. Validation of a clinicopathological score for the prediction of post­‑surgical evolution of pituitary adenoma: retrospective analysis on 566 patients from a tertiary care centre. Eur J Endocrinol. 2019;180(2):127-134. doi:10.1530/EJE-18-0749. Go to original source... Go to PubMed...
  7. Colao A, Pivonello R, Scarpa R, et al. The acromegalic arthropathy. J Endocrinol Invest. 2005;28(8 Suppl.):24-31.
  8. Drummond J, Roncaroli F, Grossman AB, et al. Clinical and Pathological Aspects of Silent Pituitary Adenomas. J Clin Endocrinol Metab. 2019;104(7):2473-2489. doi:10.1210/jc.2018-00688. Go to original source... Go to PubMed...
  9. Ezzat S, Asa SL, Couldwell WT, et al. The prevalence of pituitary adenomas: a systematic review. Cancer. 2004;101(3):613-619. doi:10.1002/cncr.20412. Go to original source... Go to PubMed...
  10. Fassett DR, Couldwell WT. Metastases to the pituitary gland. Neurosurg Focus. 2004;16(4):E8. Go to original source...
  11. Guerrero­‑Perez F, Marengo AP, Vidal N, et al. Primary tumors of the posterior pituitary: a systematic review. Rev Endocr Metab Disord. 2019;20(2):219-238. doi:10.1007/s11154-019-09484-1. Go to original source... Go to PubMed...
  12. Chen J, Jian X, Deng S, et al. Identification of recurrent USP48 and BRAF mutations in Cushing's disease. Nat Commun. 2018;9(1):3171. doi:10.1038/s41467-018-05275-5. Go to original source... Go to PubMed...
  13. Kaltsas GA, Powles TB, Evanson J, et al. Hypothalamo­‑pituitary abnormalities in adult patients with langerhans cell histiocytosis: clinical, endocrinological, and radiological features and response to treatment. J Clin Endocrinol Metab. 2020;85(4):1370-1376. doi:10.1210/jcem.85. 4. 6501. Go to original source...
  14. Kwancharoen R, Blitz AM, Tavares F, et al. Clinical features of sellar and suprasellar meningiomas. Pituitary. 2014;17(4):342-348. doi:10.1007/s11102-013-0507-z. Go to original source... Go to PubMed...
  15. Lavrentaki A, Paluzzi A, Wass JA, et al. Epidemiology of acromegaly: review of population studies. Pituitary. 2017;20(1):4-9. doi:10.1007/s11102-016-0754-x. Go to original source... Go to PubMed...
  16. Lopes MB, Sloan E, Polder J. Mixed Gangliocytoma­‑Pituitary Adenoma: Insights on the Pathogenesis of a Rare Sellar Tumor. Am J Surg Pathol. 2017;41(5):586-595. doi:10.1097/PAS.0000000000000806. Go to original source... Go to PubMed...
  17. Lu L, Wan X, Xu Y, et al. Prognostic Factors for Recurrence in Pituitary Adenomas: Recent Progress and Future Directions. Diagnostics (Basel). 2022;12(4). doi:10.3390/diagnostics12040977. Go to original source... Go to PubMed...
  18. McDowell BD, Wallace RB, Carnahan RM, et al. Demographic differences in incidence for pituitary adenoma. Pituitary. 2011;14(1):23-30. doi:10.1007/s11102-010-0253-4. Go to original source... Go to PubMed...
  19. Mete O, Lopes MB, Asa SL. Spindle cell oncocytomas and granular cell tumors of the pituitary are variants of pituicytoma. Am J Surg Pathol. 2013;37(11):1694-1699. doi:10.1097/PAS.0b013e31829723e7. Go to original source... Go to PubMed...
  20. Muller HL, Merchant TE, Warmuth­‑Metz M, et al. Cranio­pharyngioma. Nat Rev Dis Primers. 2019;5(1):75. doi:10.1038/s41572-019-0125-9. Go to original source... Go to PubMed...
  21. Neou M, Villa C, Armignacco R, et al. Pangenomic Classification of Pituitary Neuroendocrine Tumors. Cancer Cell. 2020;37(1):123-134 e125. doi:10.1016/j.ccell.2019. 11. 002. Go to original source...
  22. Nishioka H, Inoshita N, Mete O, et al. The Complementary Role of Transcription Factors in the Accurate Diagnosis of Clinically Nonfunctioning Pituitary Adenomas. Endocr Pathol. 2015;26(4):349-355. doi:10.1007/s12022-015-9398-z. Go to original source... Go to PubMed...
  23. Ostrom QT, Francis SS, Barnholtz­‑Sloan JS. Epidemiology of Brain and Other CNS Tumors. Curr Neurol Neurosci Rep. 2021;21(12):68. doi:10.1007/s11910-021-01152-9. Go to original source... Go to PubMed...
  24. Ostrom QT, Gittleman H, Truitt G, et al. CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2011-2015. Neuro Oncol. 2018;20(suppl_4), iv1-iv86. doi:10.1093/neuonc/noy131. Go to original source... Go to PubMed...
  25. Papanikolaou N, Millar O, Coulden A, et al. Clinical characteristics of functioning gonadotroph adenoma in women presenting with ovarian hyperstimulation: Audit of UK pituitary centres. Clin Endocrinol (Oxf). 2023;99(4):386-395. doi:10.1111/cen.14949. Go to original source... Go to PubMed...
  26. Ragnarsson O, Olsson DS, Chantzichristos D, et al. The incidence of Cushing's disease: a nationwide Swedish study. Pituitary. 2019;22(2):179-186. doi:10.1007/s11102-019-00951-1. Go to original source... Go to PubMed...
  27. Shimon I. Metastatic Spread to the Pituitary. Neuroendocrinology. 2020;110(9-10):805-808. doi:10.1159/000506810. Go to original source... Go to PubMed...
  28. Schmid S, Solomon DA, Perez E, et al. Genetic and epigenetic characterization of posterior pituitary tumors. Acta Neuropathol. 2021;142(6):1025-1043. doi:10.1007/s00401-021-02377-1. Go to original source... Go to PubMed...
  29. Teears RJ, Silverman EM. Clinicopathologic review of 88 cases of carcinoma metastatic to the putuitary gland. Cancer. 1975;36(1):216-220. doi:10.1002/1097-0142(197507)36:13. 0. co;2-e. Go to original source...
  30. Trouillas J, Roy P, Sturm N, et al. A new prognostic clinicopathological classification of pituitary adenomas: a multicentric case­‑control study of 410 patients with 8 years post­‑operative follow­‑up. Acta Neuropathol. 2013;126(1):123-135. doi:10.1007/s00401-013-1084-y. Go to original source... Go to PubMed...
  31. Villa C, Vasiljevic A, Jaffrain­‑Rea ML, et al. A standardised diagnostic approach to pituitary neuroendocrine tumours (PitNETs): a European Pituitary Pathology Group (EPPG) proposal. Virchows Arch. 2019a;475(6):687-692. doi:10.1007/s00428-019-02655-0. Go to original source... Go to PubMed...
  32. Villa C, Vasiljevic A, Jaffrain­‑Rea ML, et al. A standardised diagnostic approach to pituitary neuroendocrine tumours (PitNETs): a European Pituitary Pathology Group (EPPG) proposal. Virchows Arch. 2019 b. doi:10.1007/s00428-019-02655-0 Go to original source... Go to PubMed...
  33. WHO. (2021). World Health Organization Classification of Tumours of the Central Nervous System. (5th ed.). Lyon: International Agency for Research on Cancer.




Neurology for Practice

Madam, Sir,
please be aware that the website on which you intend to enter, not the general public because it contains technical information about medicines, including advertisements relating to medicinal products. This information and communication professionals are solely under §2 of the Act n.40/1995 Coll. Is active persons authorized to prescribe or supply (hereinafter expert).
Take note that if you are not an expert, you run the risk of danger to their health or the health of other persons, if you the obtained information improperly understood or interpreted, and especially advertising which may be part of this site, or whether you used it for self-diagnosis or medical treatment, whether in relation to each other in person or in relation to others.

I declare:

  1. that I have met the above instruction
  2. I'm an expert within the meaning of the Act n.40/1995 Coll. the regulation of advertising, as amended, and I am aware of the risks that would be a person other than the expert input to these sites exhibited


No

Yes

If your statement is not true, please be aware
that brings the risk of danger to their health or the health of others.