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Adrenal Gland - Amyloid

Image of amyloid in the adrenal gland from a male B6C3F1/N mouse in a chronic study
Adrenal gland, Cortex - Amyloid in a male B6C3F1/N mouse from a chronic study. There is homogeneous, amorphous, pale eosinophilic material (amyloid, A) expanding the zona fasciculata and zona reticularis; C = cortex, M = medulla.
Figure 1 of 6
Image of amyloid in the adrenal gland from a male B6C3F1/N mouse in a chronic study
Adrenal gland, Cortex - Amyloid in a male B6C3F1/N mouse from a chronic study (higher magnification of Figure 1). The homogeneous, amorphous, pale eosinophilic material (amyloid, A) in the zona fasciculata and zona reticularis separates and replaces the cortical cells; C = cortex, M = medulla.
Figure 2 of 6
Image of amyloid in the adrenal gland from a male Swiss Webster mouse in a chronic study
Adrenal gland, Cortex - Amyloid in a male Swiss Webster mouse from a chronic study. A thick circumferential band of homogeneous, amorphous, pale eosinophilic material (amyloid, A) largely replaces the cells of the zona reticularis; C = cortex, M = medulla.
Figure 3 of 6
Image of amyloid in the adrenal gland from a female B6C3F1/N mouse in a chronic study
Adrenal gland, Cortex - Amyloid in a female B6C3F1/N mouse from a chronic study. Abundant, homogeneous, amorphous, pale eosinophilic material (amyloid, A) separates and replaces the cells inner cortex; C = cortex, M = medulla.
Figure 4 of 6
Image of amyloid in the adrenal gland from a female B6C3F1/N mouse in a chronic study
Adrenal gland, Cortex - Amyloid in a female B6C3F1/N mouse from a chronic study (same animal as in Figure 4). Amyloid deposits in the inner cortex (arrow) stained with Congo red appear dull reddish orange under nonpolarized light.
Figure 5 of 6
Image of amyloid in the adrenal gland from a female B6C3F1/N mouse in a chronic study
Adrenal gland, Cortex - Amyloid in a female B6C3F1/N mouse from a chronic study (same animal as in Figure 4). Amyloid deposits in the inner cortex (arrow) stained with Congo red have a characteristic �apple green� birefringence under polarized light.
Figure 6 of 6
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comment:

The term "amyloid" classically denotes various insoluble, fibrillar proteins that share a similar configuration (β-pleated sheets). These abnormally folded proteins form and accumulate intra- and extracellularly in many tissues due to many causes, such as genetic predisposition and local and systemic inflammation of various etiologies. In rats, focal or generalized amyloid deposition rarely occurs in any tissue, including the adrenal gland. In mice, amyloid deposition in the adrenal gland and other tissues is overall far more common. There are genetically related differences in incidence, with very low incidences in some strains, such as the B6C3F1/N mouse, and much higher incidences in other strains, such as (Swiss) CD-1 and Swiss Webster mice. In mice, amyloidosis is usually a spontaneous, age-related systemic disease, with the adrenal gland one of the more commonly affected tissues. Severity (amount of amyloid/tissue) also tends to increase with age in all tissues, including the adrenal gland. In mice, adrenal amyloid deposition usually first appears as small clumps between cells of the inner cortex, with progressive centripetal extension into the outer cortex (zona fasciculata) ( Figure 1image opens in a pop-up window , Figure 2image opens in a pop-up window , Figure 3image opens in a pop-up window , Figure 4image opens in a pop-up window , Figure 5image opens in a pop-up window , and Figure 6image opens in a pop-up window ). The amyloid proteins can form large, expansile aggregates ( Figure 1image opens in a pop-up window and Figure 2image opens in a pop-up window ), which distort the normal architecture and can eventually coalesce into thick circumferential bands that surround the medulla ( Figure 3image opens in a pop-up window and Figure 4image opens in a pop-up window ). The amyloid may extend into the medulla or zona glomerulosa, but these regions are generally unaffected.

With hematoxylin and eosin (H&E) stain, amyloid deposits appear as homogeneous, amorphous, pale eosinophilic material ( 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 ). Special histochemical stains are often used to distinguish amyloid from fibrous connective tissue, fibrin, and other substances. One of the most widely used stains is Congo red. Amyloid stained with Congo red appears pale to dull red under nonpolarized light ( Figure 5image opens in a pop-up window ) but exhibits brilliant birefringence (usually "apple green") under polarized light ( Figure 6image opens in a pop-up window ). Other methods for amyloid detection include fluorescent or metachromatic stains and immunohistochemistry.

recommendation:

Amyloid in the adrenal should be diagnosed as present without assignment of a severity grade. Any associated loss or degeneration of cells should not be diagnosed separately but should be described in the pathology narrative. Whether the adrenal amyloid deposits are localized or part of a systemic distribution should also be addressed in the narrative. If amyloid is seen in both adrenal glands, the modifier "bilateral" should be added to the diagnosis (lesions are assumed to be unilateral unless otherwise indicated).

references:

Brayton CF, Treuting PM, Ward JM. 2012. Pathobiology of aging mice and GEM: Background strains and experimental design. Vet Pathol 49:85-105.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/22215684

Elghetany MT, Saleem A. 1988. Methods for staining amyloid in tissues: A review. Stain Technol 63:201-212.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/2464206

Hamlin MH, Banas DA. 1990. Adrenal gland. In: Pathology of the Fischer Rat: Reference and Atlas (Boorman GA, Eustis SL, Elwell MR, Montgomery CA, MacKenzie WF, eds). Academic Press, San Diego, 501-518.
Abstract: https://www.ncbi.nlm.nih.gov/nlmcatalog/9002563

Howie AJ, Brewer DB, Howell D, Jones AP. 2008. Physical basis of colors seen in Congo red-stained amyloid in polarized light. Lab Invest 88:232-242.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/18166974

National Toxicology Program. 1993. NTP TR-417. Toxicology and Carcinogenesis Studies of p-Nitrophenol (CAS No. 100-02-7) in Swiss Webster Mice (Dermal Studies). NTP, Research Triangle Park, NC.
Abstract: https://ntp.niehs.nih.gov/go/7714

National Toxicology Program. 2010. NTP TR-558. Toxicology and Carcinogenesis Studies of 3,3',4,4'-Tetrachloroazobenzene (TCAB) [CAS No. 14047-09-7] in Harlan Sprague-Dawley Rats and B6C3F1 Mice (Gavage Studies). NTP, Research Triangle Park, NC.
Abstract: https://ntp.niehs.nih.gov/go/33564

National Toxicology Program. 2012. NTP TR-576. Toxicology and Carcinogenesis Studies of Trimethylpropane Triacrylate (Technical Grade) (CAS No. 15625-89-5) in F344/N Rats and B6C3F1/N Mice (Dermal Studies). NTP, Research Triangle Park, NC.
Abstract: https://ntp.niehs.nih.gov/go/37176

Nyska A, Maronpot RR. 1990. Adrenal gland. In: Pathology of the Mouse: Reference and Atlas (Maronpot RR, Boorman GA, Gaul BW, eds). Cache River Press, Vienna, IL, 509-536.
Abstract: http://www.cacheriverpress.com/books/pathmouse.htm

Rosol TJ, Yarrington JT, Latendresse J, Capen CC. 2001. Adrenal gland: Structure, function, and mechanisms of toxicity. Toxicol Pathol 29:41-48.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/11215683

Sass B. 1983. Amyloidosis, adrenal, mouse. In: Monographs on the Pathology of Laboratory Animals: Endocrine System (Jones TC, Mohr U, Hunt RD, eds). Springer, Berlin, 57-59.
Abstract: http://www.springer.com/medicine/pathology/book/978-3-642-64649-2

Yarrington JT. 1996. Adrenal cortex. In: Pathobiology of the Aging Mouse, Vol 1 (Mohr U, Dungworth DL, Capen CC, Carlton WW, Sundberg JP, Ward JM, eds). International Life Sciences Press, Washington, DC, 124-133.

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Web page last updated on: December 30, 2014