Abstract
Histopathologically, most cases of episcleritis and diffuse or nodular scleritis show chronic, nongranulomatous inflammation with lymphocytes and plasma cells, vascular dilatation, and edema. By contrast, most cases of necrotizing scleritis show chronic granulomatous inflammation with epithelioid cells, multinucleated giant cells, lymphocytes, plasma cells, and less often neutrophils, along with inflammatory microangiopathy. Mast cells and eosinophils can sometimes be seen in the granuloma and around vessels.
In infectious scleritis, stainings and cultures of scleral scrapings may demonstrate the microorganism implicated. However, when scrapings are negative, analysis of conjunctival and scleral specimens by histopathology (stainings and cultures), tissue homogenization (PCR, culture, or cell culture lines), and indirect immunofluorescence (antimicrobe antibodies) techniques may be important for microbe isolation.
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de la Maza, M.S., Tauber, J., Foster, C.S. (2012). Pathology in Scleritis. In: The Sclera. Springer, Boston, MA. https://doi.org/10.1007/978-1-4419-6502-8_5
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