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Pituitary Gland - Hyperplasia

Image of hyperplasia in the pituitary gland from a female Harlan Sprague-Dawley rat in a chronic study
Pituitary Gland, Pars distalis - Hyperplasia in a female Harlan Sprague-Dawley rat from a chronic study. A small focus of hyperplasia (arrow) in the pars distalis is recognized by the paler staining cells.
Figure 1 of 7
Image of hyperplasia in the pituitary gland from a female Harlan Sprague-Dawley rat in a chronic study
Pituitary Gland, Pars distalis - Hyperplasia in a female Harlan Sprague-Dawley rat from a chronic study. Higher magnification of Figure 1 shows the focus of hyperplasia in greater detail.
Figure 2 of 7
Image of hyperplasia in the pituitary gland from a female Harlan Sprague-Dawley rat in a chronic study
Pituitary Gland, Pars distalis - Hyperplasia in a female Harlan Sprague-Dawley rat from a chronic study. Higher magnification of Figure 2 highlights the larger, paler staining cells in this focus of hyperplasia in the pars distalis.
Figure 3 of 7
Image of hyperplasia in the pituitary gland from a female Harlan Sprague-Dawley rat in a chronic study
Pituitary Gland, Pars distalis - Hyperplasia in a female Harlan Sprague-Dawley rat from a chronic study. Multiple focal areas of hyperplasia consisting of paler staining cells compared with the surrounding parenchyma are present in the pars distalis.
Figure 4 of 7
Image of hyperplasia in the pituitary gland from a male F344/N rat in a chronic study
Pituitary Gland, Pars distalis - Hyperplasia in a male F344/N rat from a chronic study. The focus of hyperplasia consists of paler staining cells (compared with the surrounding normal parenchyma) and dilated blood-filled vascular structures which are consistent with minimal to mild angiectasis.
Figure 5 of 7
Image of hyperplasia in the pituitary gland from a male F344/N rat in a chronic study
Pituitary Gland, Pars intermedia - Hyperplasia in a male F344/N rat from a chronic study. This example of hyperplasia of the pars intermedia (asterisk) is characterized by a circumscribed focus of cells with abundant amphophilic cytoplasm without compression of the adjacent normal parenchyma.
Figure 6 of 7
Image of hyperplasia in the pituitary gland from a male F344/N rat in a chronic study
Pituitary Gland, Pars intermedia - Hyperplasia in a male F344/N rat from a chronic study. Higher magnification of Figure 6 shows that the hyperplastic focus in the pars intermedia is characterized by a circumscribed collection of cells with abundant amphophilic cytoplasm without compression of the adjacent normal parenchyma.
Figure 7 of 7
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comment:

Focal hyperplasia is a frequent spontaneous as well as induced change and is seen more commonly in rats than in mice. The microscopic appearance is variable but consists primarily of a single cell type that blends into the adjacent parenchyma without compression ( Figure 1image opens in a pop-up window , Figure 2image opens in a pop-up window , Figure 3image opens in a pop-up window , and Figure 4image opens in a pop-up window ). Hyperplasia is typically a combination of increased cell number and increased cell size and increases with animal age. On occasion there may be multiple foci of hyperplasia ( Figure 4image opens in a pop-up window ). Angiectasis may occur within a focus of hyperplasia ( Figure 5image opens in a pop-up window ) and may sometimes cause slight compression of adjacent parenchyma.

Focal hyperplasia of the pars intermedia ( Figure 6image opens in a pop-up window and Figure 7image opens in a pop-up window ) is less common than hyperplasia of the pars distalis. The hyperplastic cells in the pars intermedia are similar to normal pars intermedia cells, and identification of a focal proliferative lesion may rely on alteration of growth pattern or asymmetrical enlargement of the pars intermedia since there may be no compression of the adjacent parenchyma. Diffuse hyperplasia may also occur and must be distinguished from a tangential section of the pars intermedia. Diffuse hyperplasia is usually of a specific cell type that can be confirmed by immunohistochemistry and typically represents a physiologic response.

There is a morphologic continuum between hyperplasia and pituitary neoplasia, with compression of the adjacent parenchyma being a primary diagnostic feature of neoplasia. Immunohistochemistry for pituitary hormones can be used to determine cell type.

recommendation:

Focal hyperplasia should be diagnosed and given a severity grade whenever present, and the part of the pituitary involved should be specified in the diagnosis (e.g., Pituitary Gland, Pars distalis - Hyperplasia). Any remarkable features of hyperplasia may be described in the pathology narrative. Angiectasis within the hyperplastic lesion should not be diagnosed separately.

references:

Capen CC. 1983. Functional and pathologic interrelationships of the pituitary gland and hypothalamus. In: Endocrine System (Jones TC, Mohr U, Hunt RD, eds). Springer, New York, 103-120.
Abstract: http://www.springer.com/medicine/pathology/book/978-3-642-96722-1

Capen CC, DeLellis RA, Yarrington JT. 1991. Endocrine system. In: Handbook of Toxicologic Pathology (Haschek WM, Rousseaux CG, eds). Academic Press, New York, 697-705.
Abstract: http://www.sciencedirect.com/science/book/9780123302151

Carlton WW, Gries CL. 1983. Cysts, pituitary; rat, mouse, and hamster. In: Endocrine System (Jones TC, Mohr U, Hunt RD, eds). Springer, New York, 161-163.
Abstract: http://www.springer.com/medicine/pathology/book/978-3-642-96722-1

Greaves P. 2007. Histopathology of Preclinical Toxicity Studies: Interpretation and Relevance in Drug Safety Evaluation, 3rd ed. Academic Press, Amsterdam, 953.
Abstract: http://www.sciencedirect.com/science/book/9780444527714

MacKenzie WF, Boorman GA. 1991. Pituitary gland. In: Pathology of the Fischer Rat: Reference and Atlas (Boorman G, Eustis S, Elwell M, Montgomery CA, MacKenzie W, eds). Academic Press, San Diego, 485-500.
Abstract: http://www.ncbi.nlm.nih.gov/nlmcatalog/9002563

Mahler J, Elwell M. 1999. The pituitary gland. In: Pathology of the Mouse: Reference and Atlas (Maronpot RR, Boorman GA, Gaul BW, eds). Cache River Press, Vienna, IL, 491-508.
Abstract: http://www.cacheriverpress.com/books/pathmouse.htm

Tucker MJ. 1998. The endocrine system. In: Target Organ Pathology (Turton J, Hoodon J, eds). Taylor and Francis, London, 311-334.
Abstract: http://www.amazon.com/Target-Organ-Pathology-Basic-Text/dp/0748401571

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Web page last updated on: August 08, 2014