Abstract
Glaucoma is a generic term used to describe diseases in which the intraocular pressure is at a level sufficient to cause damage to the tissues within an individual eye, resulting in “glaucomatous optic neuropathy”. Around 30% of the globes received in the laboratory will have been enucleated due to failed treatment for glaucoma. Glaucoma may be classified as primary open angle, primary acute angle closure, congenital glaucoma and secondary glaucoma where the chamber angle may be closed due to a fibrovascular membrane or where the chamber angle is open but the trabecular meshwork is blocked (e.g. with blood or tumour cells). A rapid rise in intraocular pressure will result in acute ischaemic damage to ocular tissues and may cause infarction in the optic nerve. A chronic sustained raised intraocular pressure leads to atrophy of intraocular tissues with loss of the ganglion cell layer of the retina and the prelaminar region of the optic nerve with bowing of the lamina cribrosa posteriorly. The changes of surgical intervention will also usually be evident in enucleation specimens.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Shiose Y. Intraocular pressure: new perspectives. Surv Ophthalmol. 1990;34:413–5.
Caprioli J. The ciliary epithelia and aqueous humour. In: Hart WM, editor. Adler’s physiology of the eye. St. Louis, MO; Washington, DC; Toronto, ON: CV Mosby; 1992. p. 228–47.
Iwamoto Y, Tamura M. Immunocytochemical study of intermediate filaments in cultured human trabecular cells. Invest Ophthalmol Vis Sci. 1988;29:244–50.
Yue BYTJ. The extracellular matrix and its modulation in the trabecular meshwork. Surv Ophthalmol. 1996;40:379–90.
Toris CB, Yablonski ME, Wang Y-L, Camras CB. Aqueous humour dynamics in the aging human eye. Am J Ophthalmol. 1999;127:407–12.
Epstein DL, Rohen JW. Morphology of the trabecular meshwork and inner wall endothelium after cationized ferritin perfusion in the monkey eye. Invest Ophthalmol Vis Sci. 1991;32:160–71.
Ainsworth JR, Lee WR. Effects of age and high pressure fixation on the lining endothelium of Schlemm’s canal. Invest Ophthalmol Vis Sci. 1990;31:745–50.
Wilson MR. The myth of “21”. J Glaucoma. 1997;6:75–7.
Mudumbai RC. Clinical update on normal tension glaucoma. Semin Ophthalmol. 2013;28:173–9.
Sun X, Dai Y, Chen Y, Yu DY, Cringle SJ, Chen J, Kong X, Wang X, Jiang C. Primary angle closure glaucoma: what we know and what we don’t know. Prog Retin Eye Res. 2017;57:26–45.
Kwon YH, Fingert JH, Kuehn MH, Alward WL. Primary open-angle glaucoma. N Engl J Med. 2009;360:1113–24.
Wang X, Johnson DH. mRNA in situ hybridization of TIGR/MYOC in human trabecular meshwork cells. Invest Ophthalmol Vis Sci. 2000;41:1724–9.
Rezaie T, Child A, Hitchings R, Brice G, Miller L, Coca-Prados M, et al. Adult-onset primary open-angle glaucoma caused by mutations in optineurin. Science. 2002;295:1077–9.
Thorleifsson G, Walters GB, Hewitt AW, Masson G, Helgason A, DeWan A, et al. Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nat Genet. 2010;42(10):906–9.
Wiggs JL, Yaspan BL, Hauser MA, Kang JH, Allingham RR, Olson LM. Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genet. 2012;8:e1002654.
Civan MM. Formation of the aqueous humor: transport component and their integration. In: Civan MM, editor. The eye’s aqueous humor, vol. 62. 2nd ed. San Diego, CA: Elsevier, Inc; 2008. p. 1–45.
Weinreb RN, Aung T, Medeiros FA. The pathophysiology and treatment of glaucoma. A review. JAMA. 2014;311:1901–11.
Kinori M, Hostovsky A, Skaat A, Schwartsman J, Melamed S. A novel method for quantifying the amount of trabecular meshwork pigment in glaucomatous and nonglaucomatous eyes. J Glaucoma. 2014;1:e13–7.
Tian B, Geiger B, Epstein DL, Kaufman PL. Cytoskeletal involvement in the regulation of aqueous humor outflow. Invest Ophthalmol Vis Sci. 2000;41:619–23.
Izzotti A, Bagnis A, Saccà SC. The role of oxidative stress in glaucoma. Mutat Res. 2006;612(2):105–14.
Saccà SC, Izzotti A, Rossi P, Traverso C. Glaucomatous outflow pathway and oxidative stress. Exp Eye Res. 2007;84:389–99.
Saccà SC, Izzotti A. Focus on molecular events in the anterior chamber leading to glaucoma. Cell Mol Life Sci. 2014;71:2197–218.
Hogg P, Calthorpe M, Batterbury M, Grierson I. Aqueous humor stimulates the migration of human trabecular meshwork cells in vitro. Invest Ophthalmol Vis Sci. 2000;41:1091–8.
Alvarado J, Murphy C, Juster R. Trabecular meshwork cellularity in primary open angle glaucoma and nonglaucomatous normals. Ophthalmology. 1984;91:564–79.
Grierson I. What is open angle glaucoma? Eye. 1987;1:15–28.
Lutjen-Drecoll E, Rittig M, Rauterberg EA. Immunomicroscopical study of type VI collagen in the trabecular meshwork of normal and glaucomatous eyes. Exp Eye Res. 1989;48:139–47.
Sihota R, Goyal A, Kaur J, Gupta V, Nag TC. Scanning electron microscopy of the trabecular meshwork: understanding the pathogenesis of primary angle closure glaucoma. Indian J Ophthalmol. 2012;60(3):183–8.
Vranka J, Kelley M, Acott TS, Keller KE. Extracellular matrix in the trabecular meshwork: intraocular pressure regulation and dysregulation in glaucoma. Exp Eye Res. 2015;133:112–25.
Acott TS, Kelley MJ. Extracellular matrix in the trabecular meshwork. Exp Eye Res. 2008;86:543–61.
Rohen JW, Lutjen-Drecoll E, Flugel C, Meyer M, Grierson I. Ultrastructure of the trabecular meshwork in untreated cases of primary open angle glaucoma. Exp Eye Res. 1993;56:683–92.
Killer HE, Pircher A. Normal tension glaucoma: a review of current understanding and mechanisms of the pathogenesis. Eye (Lond). 2018;32:924–30.
Tarkkanen AH, Kivelä TT. Vascular comorbidity in patients with low-tension glaucoma. Eur J Ophthalmol. 2014;24:869–72.
Pircher A, Remonda L, Weinreb RN, Killer HE. Translaminar pressure in Cuacasian normal tension glaucoma patients. Acta Ophthalmol. 2017;95:e524–31.
Rao A, Padhy D, Das G, Sarangi S. Evolving paradigms in classification of primary angle closure glaucoma. Semin Ophthalmol. 2017;32:228–36.
Sun X, Dai Y, Chen Y, Yu DY, Cringle SJ, Chen J, et al. Primary angle closure glaucoma: what we know and what we don’t know. Prog Retin Eye Res. 2017;57:26–45.
Wright C, Tawfik MA, Waisbourd M, Katz LJ. Primary angle-closure glaucoma: an update. Acta Ophthalmol. 2016;94:217–25.
Lowe RF. Etiology of the anatomical basis for primary angle closure glaucoma. Br J Ophthalmol. 1970;54:161–9.
Lee WR. The pathology of the outflow system in primary and secondary glaucoma. Eye. 1995;9:1–23.
Lai J, Choy BN, Shum BW. Management of primary angle-closure glaucoma. Asia Pac J Ophthalmol (Phila). 2016;5:59–62.
Tripathy BJ, Tripathy RC. Neural crest origin of human trabecular meshwork and its implications for the pathogenesis of glaucoma. Am J Ophthalmol. 1989;107:583–90.
Idrees F, Vaideanu D, Fraser SG, Sowden JC, Khaw PT. A review of anterior segment dysgeneses. Surv Ophthalmol. 2006;51:213–31.
Sowden JC. Molecular and developmental mechanisms of anterior segment dysgenesis. Eye. 2007;21:1310–8.
Perry LP, Jakobiec FA, Zakka FR, Walton DS. Newborn primary congenital glaucoma: histopathologic features of the anterior chamber filtration angle. J AAPOS. 2012;16(6):565–8.
Chan JYY, Choy BNK, Ng ALK, Shum JWH. Review on the management of primary congenital glaucoma. J Curr Glaucoma Pract. 2015;9:92–9.
Hollander DA, Sarfarazi M, Stoilov I, Wood IS, Fredrick DR, Alvarado JA. Genotype and phenotype correlations in congenital glaucoma. Trans Am Ophthalmol Soc. 2006;104:183–95.
Tawara A, Inomata H. Distribution and characterisation of sulfated proteoglycans in the trabecular tissue of goniodysgenetic glaucoma. Am J Ophthalmol. 1994;117:741–55.
Furuyoshi N, Furuyoshi M, Futa R, Gottanka J, Lutjen-Drecoll E. Ultrastructural changes in the trabecular meshwork of juvenile glaucoma. Ophthalmologica. 1997;211:140–6.
Katai N, Urakawa Y, Sato Y, Miyanaga K, Segawa K, Yoshimura N. CHARGE association with congenital glaucoma due to maldevelopment of the anterior chamber angle. Acta Ophthalmol Scand. 1997;75:322–4.
Tawara A, Inomata H. Developmental immaturity of the trabecular meshwork in juvenile glaucoma. Am J Ophthalmol. 1984;98:82–97.
Moorthy RS, Mermoud A, Baerveldt G, Minckler DS, Lee PP, Rao NA. Glaucoma associated with uveitis. Surv Ophthalmol. 1997;41:361–94.
Kuchtey RW, Lowder CY, Smith SD. Glaucoma in patients with ocular inflammatory disease. Ophthalmol Clin N Am. 2005;18:421–30.
Overby DR, Clark AF. Animal models of glucocorticoid-induced glaucoma. Exp Eye Res. 2015;141:15–22.
Camras LJ, Stamer WD, Epstien D, Gonzalez P, Yuan F. Circumferential tensile stiffness of glaucomatous trabecular meshwork. Invest Ophthalmol Vis Sci. 2014;55:814–23.
Razeghinejad MR, Katz LJ. Steroid-induced iatrogenic glaucoma. Ophthalmic Res. 2012;47(2):66–80.
Ichhpujani P, Jindal A, Katz LJ. Silicone oil induced glaucoma: a review. Graefes Arch Clin Exp Ophthalmol. 2009;247:1585–93.
Scuderi G, Contestabile MT, Scuderi L, Librando A, Fenaicia V, Rahimi S. Pigment dispersion syndrome and pigmentary glaucoma: a review and update. Int Ophthalmol. 2019;39:1651–62.
Okafor K, Vinod K, Geddes SJ. Update on pigment dispersion syndrome and pigmentary glaucoma. Curr Opin Ophthalmol. 2017;28:154–60.
Niyadurupola N, Broadway DC. Pigment dispersion syndrome and pigmentary glaucoma—a major review. Clin Exp Ophthalmol. 2008;36:868–82.
Elhawy E, Kamthan G, Dong CQ, Danias J. Pseudoexfoliation syndrome, a systemic disorder with ocular manifestations. Hum Genomics. 2012;6:22.
Gottanka J, Johnson DH, Grehn F, Lütjen-Drecoll E. Histologic findings in pigment dispersion syndrome and pigmentary glaucoma. J Glaucoma. 2006;15:142–51.
Kampik A, Green WR, Quigley HA, Pierce LH. Scanning and transmission electron microscopic studies of two cases of pigment dispersion syndrome. Am J Ophthalmol. 1981;91:573–87.
McMenamin PG, Lee WR. Ultrastructural pathology of melanomalytic glaucoma. Br J Ophthalmol. 1986;70:895–906.
Teichmann KD, Karcioglu ZA. Melanocytoma of the iris with rapidly developing secondary glaucoma. Surv Ophthalmol. 1995;40:136–44.
Fineman MS, Eagle RC, Shields JA, Shields CL, De Potter P. Melanomalytic glaucoma in eyes with necrotic iris melancytoma. Ophthalmology. 1998;105:492–6.
Mavrakanas N, Axmann S, Issum CV, Schutx JS, Shaarwy T. Phacolytic glaucoma: are there 2 forms? J Glaucoma. 2012;21:248–9.
Rosenbaum JT, Samples JR, Seymour B, Langlois L, David L. Chemotactic activity of lens proteins and the pathogenesis of phacolytic glaucoma. Arch Ophthalmol. 1987;105:1582–4.
Challa P. Genetics of pseudoexfoliation syndrome. Curr Opin Ophthalmol. 2009;20:88–91.
Thorleifsson G, Magnusson KP, Sulem P, Walters GB, Gudbjartsson DF, Stefansson H, et al. Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science. 2007;317:1397–400.
Asano N, Schlotzer-Schrehardt U, Naumann GOH. A histopathologic study of iris changes in pseudoexfoliation syndrome. Ophthalmology. 1995;102:1279–90.
Borrás T. The cellular and molecular biology of the iris, an overlooked tissue. J Glaucoma. 2014;23:S39–42.
Zenkel M, Schlötzer-Schrehardt U. Expression and regulation of LOXL1 and elastin-related genes in eyes with exfoliation syndrome. J Glaucoma. 2014;23:S48–50.
Ritch R, Schlotzer-Schrehardt U. Exfoliation (pseudoexfoliation) syndrome: toward a new understanding. Proceedings of the first international think tank. Acta Ophthalmol Scand. 2001;79(2):213–7.
Ovodenko B, Rostagno A, Neubert TA, Shetty V, Thomas S, Yang A, et al. Proteomic analysis of exfoliation deposits. Invest Ophthalmol Vis Sci. 2007;48(4):1447–57.
Rasmussen CA, Kaufman PL. The trabecular meshwork in normal eyes and in exfoliation glaucoma. J Glaucoma. 2014;23:S15–9.
Conway RM, Schlötzer-Schrehardt U, Küchle M, Naumann GO. Pseudoexfoliation syndrome: pathological manifestations of relevance to intraocular surgery. Clin Exp Ophthalmol. 2004;32:199–210.
Matsuo T. Photoreceptor outer segments in aqueous humour: key to understanding a new syndrome. Surv Ophthalmol. 1994;39:211–33.
Netland PA, Sizuo M, Covington HI. Elevated intraocular pressure secondary to rhegmatogenous retinal detachment. Surv Ophthalmol. 1994;39:234–40.
Matsuo T, Muraoka N, Shiraga F, Matsuo N. Schwartz-Matsuo-syndrome in retinal detachment with tears of the nonpigmented epithelium of the ciliary body. Acta Ophthalmol Scand. 1998;76:481–5.
Clark A, Alkhotani A, Yucel YH, Sylvester C, Kertes PJ, Birt CM. Electron microscopic evidence of photoreceptor outer-segments in the trabecular meshwork in a case of Schwartz-Matsuo syndrome. J Glaucoma. 2019;28:843–5.
Morgan WH, Yu DY. Surgical management of glaucoma: a review. Clin Exp Ophthalmol. 2012;40:388–99.
Conway RM, Chua WC, Qureshi C, Billson FA. Primary iris melanoma: diagnostic features and outcome of conservative surgical treatment. Br J Ophthalmol. 2001;85(7):848–54.
Wakae H, Higashide T, Tsuneyama K, Nakamura T, Takahashi K, Sugiyama K. Immunohistochemical characterization of the ectopic epithelium devoid of goblet cells from a posttraumatic iris cyst causing mucogenic glaucoma. J Glaucoma. 2016;25:e291–4.
Sehu KW, Lee WR, editors. Ophthalmic pathology: an illustrated guide for clinicians. Malden, MA: Blackwell Publishing Ltd; 2008. ISBN 9780727917799.
Kim M, Lee C, Payne R, Yue BY, Change JH, Ying H. Angiogenesis in glaucoma filtration surgery and neovascular glaucoma: a review. Surv Ophthalmol. 2015;60:524–35.
Sun Y, Liang Y, Zhou P, Wu H, Hou X, Ren Z, et al. Anti-VEGF treatment is the key strategy for neovascular glaucoma management in the short term. BMC Ophthalmol. 2016;16:150.
Tanaka S, Ideta H, Yonemoto J, Sasaki K, Hirose A, Oka C. Neovascularization of the iris in rhegmatogenous retina detachment. Am J Ophthalmol. 1991;112:632.
Luntz MH, Rosenblatt M. Malignant glaucoma. Surv Ophthalmol. 1987;32:73–93.
Foreman-Larkin J, Netland PA, Salim S. Clinical management of malignant glaucoma. J Ophthalmol. 2015;2015:283707. 1–6.
Jonas JB, Budde WM. Diagnosis and pathogenesis of glaucomatous optic neuropathy: morphological aspects. Prog Retin Eye Res. 2000;19:1–40.
Casson RJ, Chidlow G, Wood JPM, Crowston JG, Goldberg I. Definition of glaucoma: clinical and experimental concepts. Clin Exp Ophthalmol. 2012;40:341–9.
Montgomery D. Measurement of optic disc and neuroretinal rim areas in normal and glaucomatous eyes. Ophthalmology. 1991;98:50–9.
Malik R, Swanson WH, Garway-Heath DF. ‘Structure-function relationship’ in glaucoma: past thinking and current concepts. Clin Exp Ophthalmol. 2012;40:369–80.
Grieshaber MC, Mozaffarieh M, Flammer J. What is the link between vascular dysregulation and glaucoma? Surv Ophthalmol. 2007;52:S144–54.
Pasquale LR. Vascular and autonomic dysregulation in primary open-angle glaucoma. Curr Opin Ophthalmol. 2016;27:94–101.
Nicolela MT. Clinical clues of vascular dysregulation and its association with glaucoma. Can J Ophthalmol. 2008;43:337–41.
Radius RL. Anatomy of the optic nerve head and glaucomatous optic neuropathy. Surv Ophthalmol. 1987;32:35–44.
Quigley HA, Sanchez RM, Dunkelberger GR, L’Hernault NL, Baginski TA. Chronic glaucoma selectively damages large optic nerve fibres. Invest Ophthalmol Vis Sci. 1987;28:913–20.
Jonas JB, Muller Bergh JA, Schlotzer-Schrehardt UM, Naumann GOH. Histomorphometry of the human optic nerve. Invest Ophthalmol Vis Sci. 1990;31:736–44.
Jonas JB, Fernandez MC, Naumann GOH. Correlation of the optic disc size to glaucoma susceptibility. Ophthalmology. 1991;98:675–80.
Yorio T, Krishnamoorthy R, Prasanna G. Endothelin: is it a contributor to glaucoma pathophysiology? J Glaucoma. 2002;11:259–70.
Polak K, Luksch A, Berisha F, Fuchsjager-Mayrl G, Dallinger S, Schmetterer L. Altered nitric oxide system in patients with open-angle glaucoma. Arch Ophthalmol. 2007;125:494–8.
Pournaras CJ, Rungger-Brandle E, Riva CE, Hardarson SH, Stefansson E. Regulation of retinal blood flow in health and disease. Prog Retin Eye Res. 2008;27:284–330.
Venkataraman ST, Flanagan JG, Hudson C. Vascular reactivity of optic nerve head and retinal blood vessels in glaucoma – a review. Microcirculation. 2010;17:568–81.
Miller KM, Quigley HA. The clinical appearance of the lamina cribrosa as a function of the extent of glaucomatous optic nerve damage. Ophthalmology. 1988;95:135–8.
Leung DY, Tham CC. Management of bleb complications after trabeculectomy. Semin Ophthalmol. 2013;28:144–56.
Lu LJ, Hall L, Liu J. Improving glaucoma surgical outcomes with adjunct tools. J Curr Glaucoma Pract. 2018;12:19–28.
Mietz H, Arnold G, Kirchof B, Diestelhort M, Krieglstein GK. Histopathology of episcleral fibrosis after trabeculectomy with and without mitomycin C. Graefes. Arch Clin Exp Ophthalmol. 1996;234:364–8.
Cillino S, Casuccio A, Di Pace F, Cagini C, Ferraro LL, Cillino G. Biodegradable collagen matrix implant versus mitomycin-C in trabeculectomy: five-year follow-up. BMC Ophthalmol. 2016;16:24.
Sakarya Y, Sakarya R, Kara S, Soylu T. Fibrin glue coating of the surgical surfaces may facilitate formation of a successful bleb in trabeculectomy surgery. Med Hypotheses. 2011;77:263–5.
Sethi P, Patel RN, Goldhardt R, Ayyala RS. Conjunctival advancement with subconjunctival amniotic membrane draping technique for leaking cystic blebs. J Glaucoma. 2016;25:188–92.
Hampton C, Shields MB. Transscleral neodymium-YAG cyclophotocoagulation: a histologic study of human autopsy eyes. Arch Ophthalmol. 1988;106:1121–3.
Ndulue JK, Rahmatnejad K, Sanvicente C, Wizov SS, Moster MR. Evolution of cyclophotocoagulation. J Ophthalmic Vis Res. 2018;13:55–61.
Van Buskirk EM. Pathophysiology of laser trabeculoplasty. Surv Ophthalmol. 1989;33:264–72.
Garg A, Gazzard G. Selective laser trabeculoplasty: past, present, and future. Eye (Lond). 2018;32:863–76.
Tsang S, Cheng J, Lee JWY. Developments in laser trabeculoplasty. Br J Ophthalmol. 2016;100:94–7.
Melamed S, Fiore PM. Molteno implant surgery in refractory glaucoma. Surv Ophthalmol. 1990;34:441–8.
Giovingo M. Complications of glaucoma drainage device surgery: a review. Semin Ophthalmol. 2014;29:397–402.
Aref AA, Gedde SJ, Budenz DL. Glaucoma drainage implant surgery. Dev Ophthalmol. 2017;59:43–52.
Loeffler KU, Jay JL. Tissue response to aqueous drainage in a functioning Molteno implant. Br J Ophthalmol. 1988;72:29–35.
Classen L, Kivela T, Tarkkaanen A. Histopathologic and immunohistochemical analysis of the filtration bleb after unsuccessful glaucoma seton operation. Am J Ophthalmol. 1996;122:205–12.
Eftekhari K, Shindler KS, Lee V, Dine K, Eckstein LA, Reza VM. Histologic evidence of orbital inflammation from retrobulbar alcohol and chlorpromazine injection: a clinicopathologic study in human and rat orbits. Ophthal Plast Reconstr Surg. 2016;32:302–4.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
Copyright information
© 2021 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Roberts, F., Thum, C.K. (2021). Absolute Glaucoma. In: Lee's Ophthalmic Histopathology. Springer, Cham. https://doi.org/10.1007/978-3-030-76525-5_3
Download citation
DOI: https://doi.org/10.1007/978-3-030-76525-5_3
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-76524-8
Online ISBN: 978-3-030-76525-5
eBook Packages: MedicineMedicine (R0)