U.S. flag

An official website of the United States government

Dot gov

The .gov means it's official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Skip to Main Navigation
Skip to Page Content
Skip to Atlas Navigation

Eye, Cornea - Neovascularization

Image of cornea neovascularization in the eye from a male F344/N rat in a chronic study
Eye, Cornea - Neovascularization in a male F344/N rat from a chronic study. There are multiple small blood vessels in the stroma (arrows) with concurrent inflammation and epithelial hyperplasia.
Figure 1 of 2
Image of cornea neovascularization in the eye from a male F344/N rat in a chronic study
Eye, Cornea - Neovascularization in a male F344/N rat from a chronic study (higher magnification of Figure 1). Multiple small blood vessels are proliferating in the stroma (arrows); there is concurrent stromal inflammation.
Figure 2 of 2
next arrow

comment:

The corneal stroma is normally avascular, but damage from various causes may result in neovascularization. Corneal neovascularization ( Figure 1image opens in a pop-up window and Figure 2image opens in a pop-up window ) is characterized by the proliferation of multiple small blood vessels in the corneal stroma. There is often concurrent stromal inflammation and epithelial hyperplasia. In most cases of neovascularization, the primary insult is inflammation resulting from various causes. However, neovascularization can also develop in the cornea of laboratory rodents fed diets deficient in certain nutrients.

recommendation:

When neovascularization occurs without concurrent inflammation, it should be diagnosed and assigned a severity grade. When neovascularization is considered a feature of inflammation, it should not be diagnosed separately, unless warranted by severity, but should be described in the pathology narrative.

references:

Ecoiffier T, Yuen D, Chen L. 2010. Differential distribution of blood and lymphatic vessels in the murine cornea. Invest Ophthalmol Vis Sci 51:2436-2440.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/20019372

Frame SR, Slone TW. 1966. Nonneoplastic and neoplastic changes in the eye. In: Pathobiology of the Aging Mouse, Vol 2 (Mohr U, Dungworth DL, Capen CC, Carlton WW, Sundberg JP, Ward JM, eds). ILSI Press, Washington, DC, 97-103.

Geiss V, Yoshitomi K. 1991. Eyes. In: Pathology of the Mouse: Reference and Atlas (Maronpot RR, Boorman GA, Gaul BW, eds). Cache River Press, Vienna, IL, 471-489.
Abstract: http://www.cacheriverpress.com/books/pathmouse.htm

Greaves P. 2007. Nervous system and special sense organs. In: Histopathology of Preclinical Toxicity Studies: Interpretation and Relevance in Drug Safety Evaluation, 3rd ed. Academic Press, San Diego, CA, 861-933.
Abstract: http://www.sciencedirect.com/science/book/9780444527714

Hoffart L, Matonti F, Conrath J, Daniel L, Ridings B, Masson GS, Chavane F. 2010. Inhibition of corneal neovascularization after alkali burn: Comparison of different doses of bevacizumab in monotherapy or associated with dexamethasone. Clin Exp Ophthalmol 38:346-353.
Full Text: http://onlinelibrary.wiley.com/doi/10.1111/j.1442-9071.2010.02252.x/full

National Toxicology Program. 1988. NTP TR-331. Toxicology and Carcinogenesis Studies of Malonaldehyde, Sodium Salt (3-Hydroxy-2-propenal, Sodium Salt) (CAS No. 24382-04-5) in F344/N Rats and B6C3F1 Mice (Gavage Studies). NTP, Research Triangle Park, NC.
Abstract: https://ntp.niehs.nih.gov/go/8898

Pauly A, Brignole-Baudouin, Labbé A, Liang H, Warnet J-M, Baudouin C. 2007. New tools for the evaluation of toxic ocular surface changes in the rat. Invest Ophthalmol Vis Sci 48:5473–5463.
Full Text: https://doi.org/10.1167/iovs.06-0728

Smith RS, Hawes NL, Chang B, Nishina PM. 2002. Retina. In: Systematic Evaluation of the Mouse Eye: Anatomy, Pathology, and Biomethods (Smith RS, John SWM, Nishina PM, Sundberg JP, eds). CRC Press, Boca Raton, FL, 195-225.

Taradach C, Greaves P, Rubin LF. 1984. Spontaneous eye lesions in laboratory animals: Incidence in relation to age. Crit Rev Toxicol 12:121-147.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/6368130

Yoshitomi K, Boorman GA. 1990. Eye and associated glands. In: Pathology of the Fischer Rat: Reference and Atlas (Boorman GA, Eustis SL, Elwell MR, Montgomery CA, MacKenzie WF, eds). Academic Press, San Diego, CA, 239-260.
Abstract: https://www.ncbi.nlm.nih.gov/nlmcatalog/9002563

Yudkin AM, Lambert RM. 1923. Pathogenesis of the ocular lesions produced by a deficiency of vitamin A. J Exp Med 38:17-24.
Full Text: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2128416/pdf/17.pdf