J Pathol Transl Med.  2016 Nov;50(6):419-425. 10.4132/jptm.2016.06.30.

The Predictive Value of Pathologic Features in Pituitary Adenoma and Correlation with Pituitary Adenoma Recurrence

Affiliations
  • 1Department of Hospital Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea. lys9908@catholic.ac.kr
  • 2Department of Hospital Pathology, Soonchunhyang University Hospital, Bucheon, Korea.
  • 3Department of Neurosurgery, College of Medicine, The Catholic University of Korea, Seoul, Korea.

Abstract

BACKGROUND
The 2004 World Health Organization classification introduced atypical pituitary adenoma (aPA), which was equivocally defined as invasion with increased mitotic activity that had a Ki-67 labeling index (LI) greater than 3%, and extensive p53 immunoreactivity. However, aPAs that exhibit all of these features are rare and the predictive value for recurrence in pituitary adenomas (PAs) remains uncertain. Thus, we sought to characterize pathological features of PAs that correlated with recurrence.
METHODS
One hundred and sixty-seven cases of surgically resected PA or aPA were retrieved from 2011 to 2013 in Seoul St. Mary's Hospital. Among them, 28 cases were confirmed to be recurrent, based on pathologic or radiologic examination. The pathologic characteristics including mitosis, invasion, Ki-67 LI and p53 immunoreactivity were analyzed in relation to recurrence.
RESULTS
Analysis of the pathologic features indicated that only Ki-67 LI over 3% was significantly associated with tumor recurrence (p = .02). The cases with at least one pathologic feature showed significantly higher recurrence rates (p < .01). Analysis indicated that cases with two pathologic features, Ki-67 LI over 3% and extensive p53 immunoreactivity 20% or more, were significantly associated with tumor recurrence (p < .01).
CONCLUSIONS
Based on these results, PA tumor recurrence can be predicted by using mitosis, invasion, Ki-67 LI (3%), or extensive p53 immunoreactivity (≥ 20%). Assessment of these features is recommended for PA diagnosis for more accurate prediction of recurrence.

Keyword

Pituitary neoplasms; Recurrence; Ki-67 antigen; Tumor suppressor protein p53

MeSH Terms

Classification
Diagnosis
Ki-67 Antigen
Mitosis
Pituitary Neoplasms*
Recurrence*
Seoul
Tumor Suppressor Protein p53
World Health Organization
Ki-67 Antigen
Tumor Suppressor Protein p53

Figure

  • Fig. 1. Microscopic findings of an atypical pituitary adenoma case with sphenoid sinus and dura invasion. (A) Tumor cells invading the sphenoid sinus. (B) Foci of tumor cell infiltration into the dura. (C) Tumor cells show extensive p53 immunoreactivity. (D) High Ki-67 labeling index (about 40%) is noted.

  • Fig. 2. Microscopic findings of a pituitary carcinoma case with metastasis to the distant cerebrum and skull. (A) The tumor cells metastasize to the cerebrum. (B) The skull bone tissue is infiltrated by the metastatic tumor cells. (C) Infiltrating tumor cells with mitotic activity. (D) High Ki-67 labeling index (about 15%) is observed.


Cited by  1 articles

Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas
Su Jung Kum, Hye Won Lee, Soon Gu Kim, Hyungsik Park, Ilseon Hwang, Sang Pyo Kim
J Pathol Transl Med. 2022;56(1):22-31.    doi: 10.4132/jptm.2021.08.31.


Reference

1. DeLellis RA, Lloyd RV, Heitz PU, Eng C. World Health Organization classification of tumours: pathology and genetics of tumours of endocrine organs. Lyon: IARC Press;2004.
2. Kaltsas GA, Nomikos P, Kontogeorgos G, Buchfelder M, Grossman AB. Clinical review: diagnosis and management of pituitary carcinomas. J Clin Endocrinol Metab. 2005; 90:3089–99.
3. Fernandez A, Karavitaki N, Wass JA. Prevalence of pituitary adenomas: a community-based, cross-sectional study in Banbury (Oxfordshire, UK). Clin Endocrinol (Oxf). 2010; 72:377–82.
Article
4. Daly AF, Rixhon M, Adam C, Dempegioti A, Tichomirowa MA, Beckers A. High prevalence of pituitary adenomas: a cross-sectional study in the province of Liege, Belgium. J Clin Endocrinol Metab. 2006; 91:4769–75.
Article
5. Saeger W, Ludecke DK, Buchfelder M, Fahlbusch R, Quabbe HJ, Petersenn S. Pathohistological classification of pituitary tumors: 10 years of experience with the German Pituitary Tumor Registry. Eur J Endocrinol. 2007; 156:203–16.
Article
6. Al-Shraim M, Asa SL. The 2004 World Health Organization classification of pituitary tumors: what is new? Acta Neuropathol. 2006; 111:1–7.
Article
7. Mete O, Ezzat S, Asa SL. Biomarkers of aggressive pituitary adenomas. J Mol Endocrinol. 2012; 49:R69–78.
Article
8. Yildirim AE, Divanlioglu D, Nacar OA, et al. Incidence, hormonal distribution and postoperative follow up of atypical pituitary adenomas. Turk Neurosurg. 2013; 23:226–31.
Article
9. Zada G, Woodmansee WW, Ramkissoon S, Amadio J, Nose V, Laws ER Jr. Atypical pituitary adenomas: incidence, clinical characteristics, and implications. J Neurosurg. 2011; 114:336–44.
Article
10. Lee EH, Kim KH, Kwon JH, Kim HD, Kim YZ. Results of immunohistochemical staining of cell-cycle regulators: the prediction of recurrence of functioning pituitary adenoma. World Neurosurg. 2014; 81:563–75.
Article
11. Sadeghipour A, Mahouzi L, Salem MM. Ki67 labeling correlated with invasion but not with recurrence. Appl Immunohistochem Mol Morphol. 2016; Feb. 9. [Epub]. https://doi.org/10.1097/PAI.0000000000000303.
Article
12. Hadzhiyanev A, Ivanova R, Nachev E, et al. Evaluation of prognostic utility of MIB-1 and p53 expression in pituitary adenomas: correlations with clinical behaviour and follow-up results. Biotechnol Biotechnol Equip. 2014; 28:502–7.
Article
13. Tortosa F, Webb SM. Atypical pituitary adenomas: 10 years of experience in a reference centre in Portugal. Neurologia. 2016; 31:97–105.
Article
14. Chiloiro S, Doglietto F, Trapasso B, et al. Typical and atypical pituitary adenomas: a single-center analysis of outcome and prognosis. Neuroendocrinology. 2015; 101:143–50.
Article
15. Szumilas M. Explaining odds ratios. J Can Acad Child Adolesc Psychiatry. 2010; 19:227–9.
16. Figarella-Branger D, Trouillas J. The new WHO classification of human pituitary tumors: comments. Acta Neuropathol. 2006; 111:71–2.
Article
17. Grossman AB. The 2004 World Health Organization classification of pituitary tumors: is it clinically helpful? Acta Neuropathol. 2006; 111:76–7.
Article
18. Kleinschmidt-DeMasters BK. Subtyping does matter in pituitary adenomas. Acta Neuropathol. 2006; 111:84–5.
Article
19. Laws ER Jr, Lopes MB. The new WHO classification of pituitary tumors: highlights and areas of controversy. Acta Neuropathol. 2006; 111:80–1.
Article
20. Maclean J, Aldridge M, Bomanji J, Short S, Fersht N. Peptide receptor radionuclide therapy for aggressive atypical pituitary adenoma/carcinoma: variable clinical response in preliminary evaluation. Pituitary. 2014; 17:530–8.
Article
21. Matsuyama J. Ki-67 expression for predicting progression of postoperative residual pituitary adenomas: correlations with clinical variables. Neurol Med Chir (Tokyo). 2012; 52:563–9.
Article
22. Miermeister CP, Petersenn S, Buchfelder M, et al. Histological criteria for atypical pituitary adenomas: data from the German pituitary adenoma registry suggests modifications. Acta Neuropathol Commun. 2015; 3:50.
Article
Full Text Links
  • JPTM
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr