Vitreous body is an intraocular structure, origin of diverse pathologies, but is also the place where cells and inflammatory mediators are released coming from several pathologic processes. These inflammatory reactions can happen in any other ocular location like choroid, retina, optic nerve, or ciliary body and vitreous humor constitutes a stagnant reservoir for these resulting substances and debris. Through the recent techniques of vitreous collecting, handling, and analysis, increasingly more sophisticated and with fewer complications, cellularity and molecules in the vitreous of challenging pathologies for the ophthalmologist can now be studied. The most usefulness for vitreous diagnosis would be the masquerade syndromes, and the best exponent in this group is the primary vitreoretinal lymphoma (PVRL), in which cytology and an IL-10/IL-6 ratio more than 1 is fundamental for the diagnosis. 1. Introduction Vitreous body is the clear gel that fills the vitreous chamber or posterior chamber (PC) of the eyeball, the space between the lens and the eyewall, whose inner layer is the neurosensorial tissue that receives and transmits the image to the central nervous system called the retina. Its functions are to give volume to the eye, to support the retina attached, and to maintain its transparency to allow light beams to reach onto the retina. Unlike the fluid in the anterior segment of the eye (aqueous humour), which is continuously replaced, vitreous humor is stagnant, and its composition remains quite constant throughout life. The vitreous gel is avascular, composed mainly of water (98-99%), and 0.9% of inorganic salts (sodium, potassium, and chloride). The remaining 0.1% is divided between protein, polysaccharide components, and ascorbic acid. Most of the protein is forming fibrils composed of a small collagen type V/XI core wrapped in a thick layer of collagen type II (75% of the fibril by mass) [1, 2]. It also contains very few cells, mostly phagocytes, whose function is to remove undesired cellular debris from the visual field, as well as hyalocytes of the surface of vitreous, which act as macrophages [3, 4]. The vitreous is feebly antigenic and is characterized by the absence of gamma-globulins and immunocompetent cells [5]. Because it only exhibits phagocytosis, this represents an incomplete and primitive immunological system, reacting like an embryonic tissue. The immune privilege, also, a physiologic mechanism characteristic of the internal compartments of the eye, is designed to provide protection against pathogens, protecting the delicate
References
[1]
D. V. Reddy and V. E. Kinsey, “Composition of the vitreous humor in relation to that of plasma and aqueous humors,” Archives of Ophthalmology, vol. 63, pp. 715–720, 1960.
[2]
D. A. Swann and I. J. Constable, “Vitreous structure. I. Distribution of hyaluronate and protein,” Investigative ophthalmology, vol. 11, no. 3, pp. 159–163, 1972.
[3]
J. A. Szirmai and E. A. Balazs, “Studies on the structure of the vitreous body. III. Cells in the cortical layer,” A.M.A. Archives of Ophthalmology, vol. 59, no. 1, pp. 34–48, 1958.
[4]
J. M. Burke, E. Sipos, and H. E. Cross, “Cell proliferation in response to vitreous hemoglobin,” Investigative Ophthalmology and Visual Science, vol. 20, no. 5, pp. 575–581, 1981.
[5]
J. Fran?ois, V. Victoria-Troncoso, and P. C. Maudgal, “Immunology of the vitreous body,” Modern Problems in Ophthalmology, vol. 16, pp. 196–207, 1976.
[6]
J. W. Streilein, K. Ohta, J. S. Mo, and A. W. Taylor, “Ocular immune privilege and the impact of intraocular inflammation,” DNA and Cell Biology, vol. 21, no. 5, pp. 453–459, 2002.
[7]
L. Q. Jiang, M. Jorquera, and J. W. Streilein, “Subretinal space and vitreous cavity as immunologically privileged sites for retinal allografts,” Investigative Ophthalmology and Visual Science, vol. 34, no. 12, pp. 3347–3354, 1993.
[8]
T. Yoshitoshi and H. Shichi, “Immunosuppressive factors in porcine vitreous body,” Current Eye Research, vol. 10, no. 12, pp. 1141–1149, 1991.
[9]
J. W. Streilein, “Anterior chamber associated immune deviation: the privilege of immunity in the eye,” Survey of Ophthalmology, vol. 35, no. 1, pp. 67–73, 1990.
[10]
N. Sugi-Ikai, M. Nakazawa, S. Nakamura, S. Ohno, and M. Minami, “Increased frequencies of interleukin-2- and interferon-γ-producing T cells in patients with active Behcet's disease,” Investigative Ophthalmology and Visual Science, vol. 39, no. 6, pp. 996–1004, 1998.
[11]
J. Biswas, R. Annamalai, and V. Krishnaraj, “Biopsy pathology in uveitis,” Middle East African Journal of Ophthalmology, vol. 18, no. 4, pp. 261–267, 2011.
[12]
A. Van Der Lelij and A. Rothova, “Diagnostic anterior chamber paracentesis in uveitis: a safe procedure?” British Journal of Ophthalmology, vol. 81, no. 11, pp. 976–979, 1997.
[13]
P. T. Finger, C. Papp, P. Latkany, M. Kurli, and C. E. Iacob, “Anterior chamber paracentesis cytology (cytospin technique) for the diagnosis of intraocular lymphoma,” British Journal of Ophthalmology, vol. 90, no. 6, pp. 690–692, 2006.
[14]
A. Rothova, J. H. de Boer, N. H. ten Dam-van Loon et al., “Usefulness of aqueous humor analysis for the diagnosis of posterior uveitis,” Ophthalmology, vol. 115, no. 2, pp. 306–311, 2008.
[15]
T. W. Harper, D. Miller, J. C. Schiffman, and J. L. Davis, “Polymerase chain reaction analysis of aqueous and vitreous specimens in the diagnosis of posterior segment infectious uveitis,” American Journal of Ophthalmology, vol. 147, no. 1, pp. 140–e2, 2009.
[16]
J. J. Augsburger, “Invasive diagnostic techniques for uveitis and simulating conditions,” Transactions of the American Ophthalmological Society, vol. 88, pp. 89–107, 1990.
[17]
S. Sarafzadeh, Z. M. Corrêa, A. Dhamija, J. J. Augsburger, and N. Trichopoulos, “Intraocular lymphoma diagnosed by fine-needle aspiration biopsy,” Acta Ophthalmologica, vol. 88, no. 6, pp. 705–710, 2010.
[18]
S. P. Donahue, R. P. Kowalski, B. H. Jewart, and T. R. Friberg, “Vitreous cultures in suspected endophthalmitis: biopsy or vitrectomy?” Ophthalmology, vol. 100, no. 4, pp. 452–455, 1993.
[19]
D. P. Han, S. R. Wisniewski, S. F. Kelsey, B. H. Doft, M. Barza, and P. R. Pavan, “Microbiologic yields and complication rates of vitreous needle aspiration versus mechanized vitreous biopsy in the endophthalmitis vitrectomy study,” Retina, vol. 19, no. 2, pp. 98–102, 1999.
[20]
N. Okhravi, H. M. A. Towler, P. Hykin, M. Matheson, and S. Lightman, “Assessment of a standard treatment protocol on visual outcome following presumed bacterial endophthalmitis,” British Journal of Ophthalmology, vol. 81, no. 9, pp. 719–725, 1997.
[21]
A. Lobo and S. Lightman, “Vitreous aspiration needle tap in the diagnosis of intraocular inflammation,” Ophthalmology, vol. 110, no. 3, pp. 595–599, 2003.
[22]
N. Eide and L. Walaas, “Fine-needle aspiration biopsy and other biopsies in suspected intraocular malignant disease: a review,” Acta Ophthalmologica, vol. 87, no. 6, pp. 588–601, 2009.
[23]
K. K. W. Li, W. M. Chan, B. S. M. Tam, J. S. K. Ng, D. S. C. Lam, and S. Lightman, “Needle tap in the diagnosis of inflammation,” Ophthalmology, vol. 111, no. 3, pp. 609–610, 2004.
[24]
R. Margolis, “Diagnostic vitrectomy for the diagnosis and management of posterior uveitis of unknown etiology,” Current Opinion in Ophthalmology, vol. 19, no. 3, pp. 218–224, 2008.
[25]
H. Quiroz-Mercado, J. Rivera-Sempertegui, T. A. MacKy et al., “Performing vitreous biopsy by perfluorocarbon-perfused vitrectomy,” American Journal of Ophthalmology, vol. 140, no. 6, pp. 1161–1163, 2005.
[26]
R. A. Zaldivar, D. F. Martin, J. T. Holden, and H. E. Grossniklaus, “Primary intraocular lymphoma: clinical, cytologic, and flow cytometric analysis,” Ophthalmology, vol. 111, no. 9, pp. 1762–1767, 2004.
[27]
G. N. Palexas, W. R. Green, M. F. Goldberg et al., “Diagnostic pars plana vitrectomy report of a 21-year retrospective study,” Transactions of the American Ophthalmological Society, vol. 93, pp. 281–314, 1995.
[28]
K. Liu, G. K. Klintworth, and L. G. Dodd, “Cytologic findings in vitreous fluids: analysis of 74 specimens,” Acta Cytologica, vol. 43, no. 2, pp. 201–206, 1999.
[29]
S. E. Coupland, N. E. Bechrakis, G. Anastassiou et al., “Evaluation of vitrectomy specimens and chorioretinal biopsies in the diagnosis of primary intraocular lymphoma in patients with Masquerade syndrome,” Graefe's Archive for Clinical and Experimental Ophthalmology, vol. 241, no. 10, pp. 860–870, 2003.
[30]
P. Mruthyunjaya, J. M. Jumper, R. McCallum, D. J. Patel, T. A. Cox, and G. J. Jaffe, “Diagnostic yield of vitrectomy in eyes with suspected posterior segment infection or malignancy,” Ophthalmology, vol. 109, no. 6, pp. 1123–1129, 2002.
[31]
J. L. Davis, D. M. Miller, and P. Ruiz, “Diagnostic testing of vitrectomy specimens,” American Journal of Ophthalmology, vol. 140, no. 5, pp. 822–829, 2005.
[32]
R. L. Johnston, A. Tufail, S. Lightman et al., “Retinal and choroidal biopsies are helpful in unclear uveitis of suspected infectious or malignant origin,” Ophthalmology, vol. 111, no. 3, pp. 522–528, 2004.
[33]
J. J. Augsburger and J. A. Shields, “Fine needle aspiration biopsy of solid intraocular tumors: indications, instrumentation and techniques,” Ophthalmic Surgery, vol. 15, no. 1, pp. 34–40, 1984.
[34]
C. L. Shields, M. A. Materin, L. Teixeira, A. Mashayekhi, A. Ganguly, and J. A. Shields, “Small choroidal melanoma with chromosome 3 monosomy on fine-needle aspiration biopsy,” Ophthalmology, vol. 114, no. 10, pp. 1919–1924, 2007.
[35]
T. A. McCannel, M. Y. Chang, and B. L. Burgess, “Multi-year follow-up of fine-needle aspiration biopsy in choroidal melanoma,” Ophthalmology, vol. 119, pp. 606–610, 2012.
[36]
J. W. Harbour, “Molecular prognostic testing in uveal melanoma: has it finally come of age?” Archives of Ophthalmology, vol. 125, no. 8, pp. 1122–1123, 2007.
[37]
J. Overgaard, “Uveal malignant melanoma. An ophthalmological or oncological disease?” Acta ophthalmologica Scandinavica, vol. 74, no. 4, p. 313, 1996.
[38]
C. Westerfeld and S. Mukai, “Retinal and choroidal biopsy,” International Ophthalmology Clinics, vol. 49, no. 1, pp. 145–154, 2009.
[39]
F. A. Jakobiec, D. J. Coleman, A. Chattock, and M. Smith, “Ultrasonically guided needle biopsy and cytologic diagnosis of solid intraocular tumors,” Ophthalmology, vol. 86, no. 9, pp. 1662–1678, 1979.
[40]
V. L. Perez, G. N. Papaliodis, D. Chu, F. Anzaar, W. Christen, and C. S. Foster, “Elevated levels of interleukin 6 in the vitreous fluid of patients with pars planitis and posterior uveitis: the Massachusetts eye & ear experience and review of previous studies,” Ocular Immunology and Inflammation, vol. 12, no. 3, pp. 193–201, 2004.
[41]
Y. El-Shabrawi, C. Livir-Rallatos, W. Christen, S. Baltatzis, and C. S. Foster, “High levels of interleukin-12 in the aqueous humor and vitreous of patients with uveitis,” Ophthalmology, vol. 105, no. 9, pp. 1659–1663, 1998.
[42]
R. B. Nussenblatt and S. M. Witcup, Palestine AG. Uveitis: Fundamentals and Clinical Practice, Mosby, St. Louis, Miss, USA, 2nd edition, 1906.
[43]
G. A. Ranking, F. A. Jakobiec, and A. A. Hidayat, “Intraocular lymphoproliferations simulating uveitis,” in Principles and Practices of Ophthalmology, D. M. Albert and F. A. Jacobiec, Eds., vol. 1, pp. 524–548, WB Saunders, Philadelphia, Pa, USA, 1994.
[44]
F. H. Theodore, “Conjunctival carcinoma masquerading as chronic conjunctivitis,” Eye, Ear, Nose & Throat monthly, vol. 46, no. 11, pp. 1419–1420, 1967.
[45]
A. Rothova, F. Ooijman, F. Kerkhoff, A. Van der Lelij, and H. M. Lokhorst, “Uveitis masquerade syndromes,” Ophthalmology, vol. 108, no. 2, pp. 386–399, 2001.
[46]
R. W. Read, E. Zamir, and N. A. Rao, “Neoplastic masquerade syndromes,” Survey of Ophthalmology, vol. 47, no. 2, pp. 81–124, 2002.
[47]
A. E. Omoti and C. E. Omoti, “Ophthalmic manifestations of lymphoma,” Annals of African Medicine, vol. 6, no. 3, pp. 89–93, 2007.
[48]
T. Sharma, J. Grewal, S. Gupta, and P. I. Murray, “Ophthalmic manifestations of acute leukaemias: the ophthalmologist's role,” Eye, vol. 18, no. 7, pp. 663–672, 2004.
[49]
Q. D. Nguyen and C. S. Foster, “Ciliary body melanoma masquerading as chronic uveitis,” Ocular Immunology and Inflammation, vol. 6, no. 4, pp. 253–256, 1998.
[50]
D. J. Fraser Jr. and R. L. Font, “Ocular inflammation and hemorrhage as initial manifestations of uveal malignant melanoma. Incidence and prognosis,” Archives of Ophthalmology, vol. 97, no. 7, pp. 1311–1314, 1979.
[51]
M. R. Kesen, D. P. Edward, L. J. Ulanski, H. H. Tessler, and D. A. Goldstein, “Pulmonary metastasis masquerading as anterior uveitis,” Archives of Ophthalmology, vol. 126, no. 4, pp. 572–574, 2008.
[52]
S. Kaushik, V. Gupta, R. Singh, R. K. Vasishta, A. Rajwanshi, and A. Gupta, “Disseminated metastasis following periampullary cancer resection Masquerading as uveitis,” Indian Journal of Ophthalmology, vol. 53, no. 1, pp. 57–59, 2005.
[53]
D. S. Minckler, R. L. Font, and L. E. Zimmerman, “Uveitis and reticulum cell sarcoma of brain with bilateral neoplastic seeding of vitreous without retinal or uveal involvement,” American Journal of Ophthalmology, vol. 80, no. 3, pp. 433–439, 1975.
[54]
J. Català-Mora, A. Parareda-Salles, C. G. Vicu?a-Mu?oz, M. Medina-Zurinaga, and J. Prat-Bartomeu, “Uveitis masquerade syndrome as a presenting form of diffuse retinoblastoma,” Archivos de la Sociedad Espa?ola de Oftalmología, vol. 84, no. 9, pp. 477–480, 2009.
[55]
C. L. Shields, F. Ghassemi, S. Tuncer, A. Thangappan, and J. A. Shields, “Clinical spectrum of diffuse infiltrating retinoblastoma in 34 consecutive eyes,” Ophthalmology, vol. 115, no. 12, pp. 2253–2258, 2008.
[56]
L. R. DeBarge, C. C. Chan, S. C. Greenberg, I. W. McLean, L. A. Yannuzzi, and R. B. Nussenblatt, “Chorioretinal, iris, and ciliary body infiltration by juvenile xanthogranuloma masquerading as uveitis,” Survey of Ophthalmology, vol. 39, no. 1, pp. 65–71, 1994.
[57]
W. P. Madigan, W. R. Raymond, K. J. Wroblewski, N. Thebpatiphat, R. H. Birdsong, and M. S. Jaafar, “A review of pediatric uveitis: Part I. Infectious causes and the Masquerade syndromes,” Journal of Pediatric Ophthalmology and Strabismus, vol. 45, no. 3, pp. 140–149, 2008.
[58]
H. Ohguro, Y. Yokoi, I. Ohguro et al., “Clinical and immunologic aspects of cancer-associated retinopathy,” American Journal of Ophthalmology, vol. 137, no. 6, pp. 1117–1119, 2004.
[59]
G. Zein, A. Berta, and C. S. Foster, “Multiple sclerosis-associated uveitis,” Ocular Immunology and Inflammation, vol. 12, no. 2, pp. 137–142, 2004.
[60]
A. N. Stangos, C. J. Pournaras, and I. K. Petropoulos, “Occult anterior-chamber metallic fragment post-phacoemulsification masquerading as chronic recalcitrant postoperative inflammation,” American Journal of Ophthalmology, vol. 139, no. 3, pp. 541–542, 2005.
[61]
K. Barton, C. E. Pavesio, H. M. A. Towler, and S. Lightman, “Uveitis presenting de novo in the elderly,” Eye, vol. 8, no. 3, pp. 288–291, 1994.
[62]
F. T. Kerkhoff, Q. J. Lamberts, P. R. Van den Biesen, and A. Rothova, “Rhegmatogenous retinal detachment and uveitis,” Ophthalmology, vol. 110, no. 2, pp. 427–431, 2003.
[63]
B. C. Amaratunge, J. E. Camuglia, and A. J. Hall, “Syphilitic uveitis: a review of clinical manifestations and treatment outcomes of syphilitic uveitis in human immunodeficiency virus-positive and negative patients,” Clinical and Experimental Ophthalmology, vol. 38, no. 1, pp. 68–74, 2010.
[64]
C. C. Dozier, R. M. Tarantola, K. Jiramongkolchai, and S. P. Donahue, “Fungal eye disease at a tertiary care center: the utility of routine inpatient consultation,” Ophthalmology, vol. 118, no. 8, pp. 1671–1676, 2011.
[65]
E. Delair, P. Latkany, A. G. Noble, P. Rabiah, R. McLeod, and A. Brézin, “Clinical manifestations of ocular toxoplasmosis,” Ocular Immunology and Inflammation, vol. 19, no. 2, pp. 91–102, 2011.
[66]
C. Sanghvi, C. Bell, M. Woodhead, C. Hardy, and N. Jones, “Presumed tuberculous uveitis: diagnosis, management, and outcome,” Eye, vol. 25, no. 4, pp. 475–480, 2011.
[67]
E. Biewald, N. Bornfeld, F. Otterbach, and K. Metz, “Ocular masquerade syndrome due to sarcoidosis,” Klinische Monatsblatter fur Augenheilkunde, vol. 227, no. 3, pp. 226–227, 2010.
[68]
J. M. Duckers, “Chronic anterior uveitis following bacille calmette-Guérin vaccination,” Journal of Pediatric Ophthalmology and Strabismus, vol. 46, no. 3, p. 186, 2009.
[69]
C. C. Barr and H. C. Joondeph, “Retinal periphlebitis as the initial clinical finding in a patient with Hodgkin's disease,” Retina, vol. 3, no. 4, pp. 253–257, 1983.
[70]
S. E. Coupland and B. Damato, “Understanding intraocular lymphomas,” Clinical and Experimental Ophthalmology, vol. 36, no. 6, pp. 564–578, 2008.
[71]
C. C. Chana, J. L. Rubensteinb, S. E. Coupland, et al., “Primary vitreoretinal lymphoma: a report from an international primary central nervous system lymphoma collaborative group symposium,” Oncologist, vol. 16, no. 11, pp. 1589–1599, 2011.
[72]
D. H. Char, B. M. Ljung, T. Miller, and T. Phillips, “Primary intraocular lymphoma (ocular reticulum cell sarcoma) diagnosis and management,” Ophthalmology, vol. 95, no. 5, pp. 625–630, 1988.
[73]
E. J. Rockwood, Z. N. Zakov, and J. W. Bay, “Combined malignant lymphoma of the eye and CNS (reticulum-cell sarcoma). Report of three cases,” Journal of Neurosurgery, vol. 61, no. 2, pp. 369–374, 1984.
[74]
D. F. Shen, Z. Zhuang, P. LeHoang et al., “Utility of microdissection and polymerase chain reaction for the detection of immunoglobulin gene rearrangement and translocation in primary intraocular lymphoma,” Ophthalmology, vol. 105, no. 9, pp. 1664–1669, 1998.
[75]
D. Benjamin, C. D. Park, and V. Sharma, “Human B cell interleukin 10,” Leukemia and Lymphoma, vol. 12, no. 3-4, pp. 205–210, 1994.
[76]
J. L. Davis, D. Solomon, R. B. Nussenblatt, A. G. Palestine, and C. C. Chan, “Immunocytochemical staining of vitreous cells: indications, techniques, and results,” Ophthalmology, vol. 99, no. 2, pp. 250–256, 1992.
[77]
S. E. Coupland, A. Perez-Canto, M. Hummel, H. Stein, and H. Heimann, “Assessment of HOPE fixation in vitrectomy specimens in patients with chronic bilateral uveitis (masquerade syndrome),” Graefe's Archive for Clinical and Experimental Ophthalmology, vol. 243, no. 9, pp. 847–852, 2005.
[78]
S. Yeh, E. D. Weichel, L. J. Faia et al., “25-gauge transconjunctival sutureless vitrectomy for the diagnosis of intraocular lymphoma,” British Journal of Ophthalmology, vol. 94, no. 5, pp. 633–638, 2010.
[79]
M. Yokota, H. Takase, Y. Imai et al., “A case of intraocular malignant lymphoma diagnosed by immunoglobulin gene rearrangement and translocation, and IL-10/IL-6 ratio in the vitreous fluid,” Nippon Ganka Gakkai zasshi, vol. 107, no. 5, pp. 287–291, 2003.
[80]
Y. Wang, D. Shen, V. M. Wang, et al., “Molecular Biomarkers for the Diagnosis of Primary Vitreoretinal Lymphoma.,” International Journal of Molecular Sciences, vol. 12, pp. 5684–5697, 2011.
[81]
J. M. Baehring, S. Androudi, J. J. Longtine et al., “Analysis of clonal immunoglobulin heavy chain rearrangements in ocular lymphoma,” Cancer, vol. 104, no. 3, pp. 591–597, 2005.
[82]
D. J. Wallace, D. Shen, G. F. Reed et al., “Detection of the bcl-2 t(14;18) translocation and proto-oncogene expression in primary intraocular lymphoma,” Investigative Ophthalmology and Visual Science, vol. 47, no. 7, pp. 2750–2756, 2006.
[83]
C. C. Chan, D. Shen, J. J. Hackett, R. R. Buggage, and N. Tuaillon, “Expression of chemokine receptors, CXCR4 and CXCR5, and chemokines, BLC and SDF-1, in the eyes of patients with primary intraocular lymphoma,” Ophthalmology, vol. 110, no. 2, pp. 421–426, 2003.
[84]
R. Margolis, O. F. M. Brasil, C. Y. Lowder et al., “Vitrectomy for the diagnosis and management of uveitis of unknown cause,” Ophthalmology, vol. 114, no. 10, pp. 1893–1897, 2007.
[85]
R. L. Johnston, A. Tufail, S. Lightman et al., “Retinal and choroidal biopsies are helpful in unclear uveitis of suspected infectious or malignant origin,” Ophthalmology, vol. 111, no. 3, pp. 522–528, 2004.
[86]
L. A. Wolf, G. F. Reed, R. R. Buggage, R. B. Nussenblatt, and C. C. Chan, “Vitreous cytokine levels,” Ophthalmology, vol. 110, no. 8, pp. 1671–1672, 2003.
[87]
R. R. Buggage, S. M. Whitcup, R. B. Nussenblatt et al., “Using interleukin 10 to interleukin 6 ratio to distinguish primary intraocular lymphoma and uveitis,” Investigative Ophthalmology and Visual Science, vol. 40, no. 10, pp. 2462–2463, 1999.
[88]
E. K. Akpek, S. M. Maca, W. G. Christen, and C. S. Foster, “Elevated vitreous interleukin-10 level is not diagnostic of intraocular- central nervous system lymphoma,” Ophthalmology, vol. 106, no. 12, pp. 2291–2295, 1999.
[89]
N. Cassoux, A. Giron, B. Bodaghi et al., “IL-10 measurement in aqueous humor for screening patients with suspicion of primary intraocular lymphoma,” Investigative Ophthalmology and Visual Science, vol. 48, no. 7, pp. 3253–3259, 2007.
[90]
M. S. Blumenkranz, T. Ward, S. Murphy, W. Mieler, G. A. Williams, and J. Long, “Applications and limitations of vitreoretinal biopsy techniques in intraocular large cell lymphoma,” Retina, vol. 12, no. 3, pp. S64–S70, 1992.
[91]
S. M. Whitcup, M. D. De Smet, B. I. Rubin et al., “Intraocular lymphoma: clinical and histopathologic diagnosis,” Ophthalmology, vol. 100, no. 9, pp. 1399–1406, 1993.
[92]
T. Sharma, J. Grewal, S. Gupta, and P. I. Murray, “Ophthalmic manifestations of acute leukaemias: the ophthalmologist's role,” Eye, vol. 18, no. 7, pp. 663–672, 2004.
[93]
M. Swartz and G. B. Schumann, “Acute leukemic infiltration of the vitreous diagnosed by pars plana aspiration,” American Journal of Ophthalmology, vol. 90, no. 3, pp. 326–330, 1980.
[94]
R. Zhioua, I. Boussen, I. Malek, and A. Ouertani, “Acute lymphoblastic leukemia and vitreous infiltration. A case study,” Journal Francais d'Ophtalmologie, vol. 24, no. 2, pp. 180–182, 2001.
[95]
T. Sakuma, R. Iseki, and A. Mimura, “Rapid cytologic diagnosis of choroidal malignant melanoma by vitreous smear,” Journal Fran?ais d'Ophtalmologie. In press.
[96]
C. W. Spraul, D. F. Martin, W. S. Hagler, and H. E. Grossniklaus, “Cytology of metastatic cutaneous melanoma to the vitreous and retina,” Retina, vol. 16, no. 4, pp. 328–332, 1996.
[97]
H. Goto, M. Usui, K. Wakamatsu, and S. Ito, “5-S-cysteinyldopa as diagnostic tumor marker for uveal malignant melanoma,” Japanese Journal of Ophthalmology, vol. 45, no. 5, pp. 538–542, 2001.
[98]
W. J. Foster, J. W. Harbour, N. M. Holekamp, G. K. Shah, and M. A. Thomas, “Pars plana vitrectomy in eyes containing a treated posterior uveal melanoma,” American Journal of Ophthalmology, vol. 136, no. 3, pp. 471–476, 2003.
[99]
C. L. Shields, J. A. Shields, N. E. Gross, G. P. Schwartz, and S. E. Lally, “Survey of 520 eyes with uveal metastases,” Ophthalmology, vol. 104, no. 8, pp. 1265–1276, 1997.
[100]
C. Rosenberg and P. T. Finger, “Cutaneous malignant melanoma metastatic to the eye, lids, and orbit,” Survey of Ophthalmology, vol. 53, no. 3, pp. 187–202, 2008.
[101]
N. Eide and P. Syrdalen, “Intraocular metastasis from cutaneous malignant melanoma,” Acta Ophthalmologica, vol. 68, no. 1, pp. 102–106, 1990.
[102]
Y. K. Chang, W. H. Chang, and C. L. Sung, “Vitreous and retinal metastasis from gastric cancer,” European Journal of Ophthalmology, vol. 20, no. 3, pp. 615–617, 2010.
[103]
R. Fukuda, T. Tanabe, H. Sawamura, et al., “Case of metastatic pulmonary carcinoma in optic disc diagnosed from results of biopsy performed during vitrectomy surgery,” Graefe's Archive for Clinical and Experimental Ophthalmology, vol. 249, no. 12, pp. 1883–1887, 2011.