Plurihormonality of pituitary adenomas in light of immunohistochemical studies.

INTRODUCTION Plurihormonality of pituitary adenomas can be defined as the ability of an adenoma to express more than one pituitary hormone. The application of immunohistochemistry to diagnose surgically removed pituitary tumours revealed that a great number of pituitary adenomas are in fact plurihormonal. However, data on the incidence and the clinical relevance of the pituitary adenoma plurihormonality are still scarce and controversial. MATERIAL AND METHODS Hundred fifty-five pituitary adenomas, surgically removed, were studied immunohistochemically with the antibodies against pituitary hormones or their subunits. Additionally, 40 adenomas were immunostained with Ki-67 antibody to evaluate the proliferative potential. RESULTS According to the World Health Organization (WHO) recommendations, we did not consider tumours expressing both FSH and LH (gonadotropinomas) or somatoprolactinomas expressing both GH and prolactin as plurihormonal. Even with this limitation, plurihormonality was found to be a frequent finding in both hormonally active and clinically non-functioning pituitary adenomas. It was shown that over one-third (36.1%) of the investigated adenomas expressed more than one hormone. Plurihormonality, especially that which is connected with co-expression of ACTH, seems to be more frequent in the recurrent tumours. Plurihormonal adenomas also possess higher Ki-67 indices, as compared to monohormonal tumours. CONCLUSIONS Plurihormonality is a frequent phenomenon in both hormonally active and clinically non-functioning pituitary adenomas. It also seems to predict a higher risk of tumour recurrence. (Pol J Endocrinol 2010; 61 (1): 63-66).

[1]  M. Coculescu Evolution under Complex Therapy of Acromegaly Due to a Pituitary Plurihormonal Adenoma with Colocalisation of GH and FSH , 2006 .

[2]  S. Asa,et al.  Plurihormonality in pituitary adenomas associated with acromegaly , 2006, Endocrine pathology.

[3]  M. Pawlikowski,et al.  Proliferating cell nuclear antigen (PCNA) expression in pituitary adenomas: relationship to the endocrine phenotype of adenoma. , 2006, Folia histochemica et cytobiologica.

[4]  J. Wass,et al.  Are Markers of Proliferation Valuable in the Histological Assessment of Pituitary Tumours? , 1999, Pituitary.

[5]  J. Wass,et al.  Non‐functioning pituitary adenomas with positive immunoreactivity for ACTH behave more aggressively than ACTH immunonegative tumours but do not recur more frequently , 2003, Clinical endocrinology.

[6]  H. Chiang,et al.  Plurihormonal pituitary adenomas: immunostaining of all pituitary hormones is mandatory for correct classification , 2001, Histopathology.

[7]  J. Burrin,et al.  Glycoprotein hormone alpha-subunit production and plurihormonality in human corticotroph tumours--an in vitro and immunohistochemical study. , 1995, European journal of endocrinology.

[8]  T. Kirino,et al.  HGH, PRL, and ACTH gene expression in clinically nonfunctioning adenomas detected with nonisotopicIn Situ hybridization method , 1995, Endocrine pathology.

[9]  T. Yoshimoto,et al.  Hormone production andc-myc protein labeling in plurihormonal pituitary adenomas , 1994, Endocrine Pathology.