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Ординатура / Офтальмология / Английские материалы / Veterinary Ocular Pathology A Comparative Review_Dubielzig, Ketring, McLellan_2010

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Non-surgical trauma

Chapter

 

 

5

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Figure 5.29  Feline post-traumatic ocular sarcoma, distribution in the globe.

(A,B) Subgross photomicrographs showing the typical distribution of the spindle cell variant of feline posttraumatic ocular sarcoma. The neoplastic tissue is dispersed circumferentially around the globe as is pointed out by the arrows in (A). The arrows in (B) point to areas of osseous metaplasia within the tumor. (C) Low magnification photomicrograph showing a carpet of neoplastic tissue just internal to the choroid.

A B

C

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Veterinary Ocular Pathology

A B C

D E

Figure 5.30  Spindle cell variant post-traumatic ocular sarcoma, histopathology. (A) Photomicrograph showing an anaplastic spindle cell variant tumor. (B,C) Photomicrographs highlight the basal lamina-like matrix between individual tumor cells with the PAS stain (B) and the Jones basement membrane stain, a silver stain (C). (D) A transmission electron micrograph showing the same matrix with broad, banded collagen fibers (arrow), a feature common to lens capsule. (E) Neoplastic cells internal to the choroid with less distinct PAS-positive staining around individual tumor cells.

Figure 5.31  p53 Staining in spindle cell variant post-traumatic ocular sarcoma. Immunohistochemistry of a spindle cell variant feline posttraumatic ocular sarcoma shows intranuclear p53-positive staining. The multinucleate cells show no staining.

108

 

 

 

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Figure 5.32  Spindle cell variant

 

 

 

 

 

 

 

post-traumatic ocular sarcoma,

 

 

 

 

 

 

 

immunohistochemistry. (A) Vimentin-

 

 

 

 

positive staining typical of a

 

 

 

 

 

 

 

mesenchymal tumor. (B) Smooth muscle

 

 

 

 

actin-positive staining, similar to

 

 

 

 

 

 

 

metaplastic lens epithelial cells seen in

 

 

 

 

posterior capsular opacification after

 

 

 

 

cataract surgery. Less that half of these

 

 

 

 

tumors stain positive with smooth muscle

 

 

 

 

actin. (C) Cytokeratin-positive staining.

 

 

 

 

About 25% of these tumors stain

 

 

 

 

 

 

 

positive with cytokeratin. (D) Collagen

 

A

B

C

IV-positive staining of the extracellular

 

matrix is consistent with basal lamina or lens capsular collagen. (E) α-Crystallin A-positive staining. This is the most common crystallin protein of the lens epithelium. (Reproduced with permission from Zeiss C J, Johnson E M, Dubielzig R R 2003 Feline intraocular tumors may arise from transformation of lens epithelium. Vet Pathol 40:355–362.)

D E

Figure 5.33  Early spindle cell variant post-traumatic ocular sarcoma. (A–C) Early feline post-traumatic sarcomas in globes that were removed for prophylactic reasons. The arrows point to the areas of early neoplastic proliferation in each globe. (D,E) Gross globe and subgross photomicrographs showing an early post-traumatic sarcoma adjacent to the ruptured lens.

A B C

D E

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Veterinary Ocular Pathology

A B C

D E F

Figure 5.34  Round-cell variant post-traumatic sarcoma. (A,B) Two gross images of a round-cell variant feline post-traumatic sarcoma. Advanced disease (A) and early disease (B). (C) Subgross photomicrograph showing the distribution of neoplastic tissue circumferentially within the globe similar to the spindle cell variant. (D) Higher magnification of (C). (E) Neoplastic round-cells survive around blood vessels in a sea of necrotic cells. (F) Immunohistochemistry (CD79a for B-cells) confirms the diagnosis of round-cell variant, but it is still unclear if these tumors are of B-cell or T-cell lineage.

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Non-surgical trauma

Chapter

 

 

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Figure 5.35  Feline post-traumatic ocular sarcoma, osteosarcoma variant, histopathology. (A,C) Subgross photomicrographs of osteosarcoma/ chondrosarcoma variant of feline post-traumatic ocular sarcoma (A, H&E; C, Alcian blue PAS). (B,D) Low

magnification photomicrographs showing neoplastic osteoid deposition (arrows) within affected globes.

A B

C D

Comparative Comments

Rarely, neoplastic or tumor-like proliferations have been described for

capsule rupture, both following trauma and post-operatively

the traumatized human eye, but no true counterpart for FPTOS has

following cataract surgery

been observed to date.

• In humans, although lens epithelial cells may proliferate and

• Ocular pleomorphic adenocarcinoma is an extremely rare intraocular

migrate, they retain their contact with the remnants of the lens

malignancy in humans that occurs in previously traumatized globes.

capsule

This tumor is also seen in dogs, as discussed in Chapter 9

• Long-established dogma, in the human ophthalmic pathology

• This neoplasm is thought to be derived from ciliary body

experience, holds that lens epithelial cells do not spontaneously

epithelial cells

give rise to neoplasia. However, our experiences that support

• In contrast to the canine and feline lens epithelium, lens epithelial

a lens epithelial cell origin for many cases of FPTOS challenge this

cells in humans have a more limited proliferative response to lens

dogma.

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Veterinary Ocular Pathology

Figure 5.36  Post-traumatic sarcoma seen early. (A) DSH, 1 year old: clinical photograph, taken after ocular trauma, showing cataract in a small, anteriorly luxated lens. Trauma resulted in lens resorption with only nucleus attached to the inferior iris (arrow). The detached retina was also observed. The cat developed feline post-traumatic sarcoma years after this clinical photograph was taken. (B) Gross photograph showing post-traumatic sarcoma 11 years after Figure 5.36A was taken. (C) Photomicrograph showing post-traumatic sarcoma, spindle cell variant (PAS stain).

A

B C

112

A B

C D

E

F

*

 

 

Non-surgical trauma

Chapter

 

 

5

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Figure 5.37  Uveitis diagnosed as

Cryptococcosis and Toxoplasmosis in a cat leading to post-traumatic sarcoma.

(A) Siamese, 7 years old: left eye represents the bilateral anterior uveitis. Chorioretinitis was also present. Based on serology, Cryptococcus and Toxoplasmosis was diagnosed as the etiology. (B) Same cat as in (A) 2 months after treatment: mild diffuse cortical opacities are developing. (C) Same cat as in (A,B) 2 weeks later: the cortical opacities are increasing in density.

(D) Same cat as in (A–C) 3 years later: the lens appears hypermature. Posterior synechia is present with vessels extending from the iris onto the lens. Iris bombe

is present and is especially obvious temporal. Histopathology demonstrated an early lens induced sarcoma. (E) Low magnification photomicrograph of the same eye, with Alcian blue PAS stain, showing hypermature cataract broad synechia and thick cellular and fibrous tissue around the wrinkled lens capsule (arrows). (F) Photomicrograph showing neoplastic spindle cells from the same eye internal to the tapetum (*).

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Veterinary Ocular Pathology

BIBLIOGRAPHY

Relative importance of non-surgical trauma

Yanoff, M., Fine, B.S., 2002. Ocular pathology, 5th edn. Mosby, St Louis.

Erie, J.C., Nevitt, M.P., Hodge, D., et al., 1992. Incidence of enucleation in a defined population. Am. J. Ophthalmol. 113, 138–144.

de Gottrau, P., Holbach, L.M., Naumann, G.O., 1994. Clinicopathological review of 1146 enucleations (1980–1990). Br. J. Ophthalmol. 78, 260–265.

Corneal effects of trauma

Walde, I., 1983. Band opacities. Equine Vet. J. (Suppl. 2), 32.

Brooks, D.E., Matthews, A.G., 2007. Equine ophthalmology. In: Gelatt, K.N. (Ed.), Veterinary ophthalmology, 4th edn. Blackwell, Oxford, pp. 1165–1274.

Kafarnik, C., Murphy, C., Dubielzig, R., 2009. Canine duplication of Descemet’s membrane. Vet. Pathol. 46, 464–473.

Bourne, W., Nelson, L., Buller, C., et al., 1994. Long-term observation of morphologic and functional features of cat corneal endothelium after wounding. Invest. Ophthalmol. Vis. Sci. 35, 891–899.

Uveal effects of trauma

Murphy, C.J., Kern, T.J., McKeever, K., et al., 1982. Ocular lesions in free-living raptors. J. Am. Vet. Med. Assoc. 181, 1302–1304.

Williams, D.L., Gonzalez Villavincencio, C.M., Wilson, S., 2006. Chronic ocular lesions in tawny owls (Strix aluco) injured by road traffic. Vet. Rec. 159, 148–153.

Lens effects of trauma

van der Woerdt, A., Nasisse, M.P., Davidson, M.G., 1992. Lens-induced uveitis in dogs: 151 cases (1985–1990). J. Am. Vet. Med. Assoc. 201, 921–926.

Van Der Woerdt, A., 2000. Lens-induced uveitis. Vet. Ophthalmol. 3, 227–234.

Grahn, B.H., Cullen, C.L., 2000. Equine phacoclastic uveitis: the clinical manifestations, light microscopic findings, and therapy of 7 cases. Can. Vet. J. 41, 376–382.

Gerardi, J.G., Colitz, C.M., Dubielzig, R.R.,

et al., 1999. Immunohistochemical analysis of lens epithelial-derived membranes following cataract extraction in the dog. Vet. Ophthalmol. 2, 163–168.

Colitz, C.M., Malarkey, D., Dykstra, M.J., et al., 2000. Histologic and immunohistochemical

characterization of lens capsular plaques in dogs with cataracts. Am. J. Vet. Res. 61, 139–143.

Bernays, M.E., Peiffer, R.L., 2000. Morphologic alterations in the anterior lens capsule of canine eyes with cataracts. Am. J. Vet. Res. 61, 1517–1519.

Davidson, M.G., Morgan, D.K., McGahan, M.C., 2000. Effect of surgical technique on in vitro posterior capsule opacification. J. Cataract Refract. Surg. 26, 1550–1554.

Davidson, M.G., Wormstone, M., Morgan, D., et al., 2000. Ex vivo canine lens capsular sac explants. Graefes Arch. Clin. Exp. Ophthalmol. 238, 708–714.

Retinal effects of trauma

Mansour, A.M., Green, W.R., Hogge, C., 1992. Histopathology of commotio retinae. Retina. 12, 24–28.

Scleral trauma

Rampazzo, A., Eule, C., Speier, S., et al., 2006. Scleral rupture in dogs, cats, and horses. Vet. Ophthalmol. 9, 149–155.

Penetrating injuries

Davidson, M.G., Nasisse, M.P., Jamieson, V.E., et al., 1991. Traumatic anterior lens capsule disruption. J. Am. Anim. Hosp. Assoc. 27, 410–414.

Chmielewski, N.T., Brooks, D.E., Smith, P.J., et al., 1997. Visual outcome and ocular

survival following iris prolapse in the horse: a review of 32 cases. Equine Vet. J. 29, 31–39.

Smith, M.M., Smith, E.M., La Croix, N., et al., 2003. Orbital penetration associated with tooth extraction. J. Vet. Dent. 20, 8–17.

Grahn, B.H., Szentimrey, D., Pharr, J.W., et al., 1995. Ocular and orbital porcupine quills in the dog: a review and case series. Can. Vet. J. 36, 488–493.

Wagoner, M.D., 1997. Chemical injuries of the eye: Current concepts in pathophysiology and therapy. Surv. Ophthalmol. 41, 275–313.

Chen, C.C., Yang, C.M., Hu, F.R., et al., 2005. Penetrating ocular injury caused by venomous snakebite. Am. J. Ophthalmol. 140, 544–546.

Proptosis

Gilger, B.C., Hamilton, H.L., Wilkie, D.A., et al., 1995. Traumatic ocular proptoses in dogs and cats: 84 cases (1980–1993). J. Am. Vet. Med. Assoc. 206, 1186–1190.

Li, Y., Schlamp, C., Nickells, R., 1999. Experimental induction of retinal ganglion cell death in adult mice. Invest. Ophthalmol. Vis. Sci. 40, 1004–1008.

Spiess, B.M., 2007. Diseases and surgery of the canine orbit. In: Gelatt, K.N. (Ed.), Veterinary ophthalmology, 4th edn.

Blackwell, Oxford, pp. 539–562.

Feline post-traumatic sarcoma

Woog, J., Albert, D.M., Gonder, J.R., et al., 1983. Osteosarcoma in a phthisical feline eye.

Vet. Pathol. 20, 209–214.

Dubielzig, R.R., 1984. Ocular sarcoma following trauma in three cats. J. Am. Vet. Med. Assoc. 184, 578–581.

Dubielzig, R.R., Everitt, J., Shadduck, J.A., et al., 1990. Clinical and morphologic features of post-traumatic ocular sarcomas in cats. Vet.

Pathol. 27, 62–65.

Dubielzig, R.R., Hawkins, K.L., Toy, K.A., et al., 1994. Morphologic features of feline ocular sarcomas in 10 cats: light microscopy, ultrastructure, and immunohistochemistry. Vet. Comp. Ophthalmol. 4, 7–12.

Cullen, C.L., Haines, D.M., Jackson, M.L., et al., 1998. The use of immunohistochemistry and the polymerase chain reaction for detection of feline leukemia virus and feline sarcoma virus in six cases of feline ocular sarcoma. Vet. Ophthalmol. 1, 189–193.

Grossniklaus, H.E., Zimmerman, L.E., Kachmer, M.L., 1990. Pleomorphic adenocarcinoma of the ciliary body. Immunohistochemical and electron microscopic features. Ophthalmology 97, 763–768.

Zeiss, C.J., Johnson, E.M., Dubielzig, R.R., 2003. Feline intraocular tumors may arise from transformation of lens epithelium. Vet. Pathol. 40, 355–362.

Carter, R.T., Giudice, C., Dubielzig, R.R., et al., 2005. Telomerase activity with

concurrent loss of cell cycle regulation in feline post-traumatic ocular sarcomas. J. Comp. Pathol. 133, 235–245.

Grahn, B.H., Peiffer, R.L., Cullen, C.L., et al., 2006. Classification of feline intraocular neoplasms based on morphology, histochemical staining, and immunohistochemical labeling. Vet. Ophthalmol. 9, 395–403.

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6

Chapter 6

Diseases of the orbit

CHAPTER CONTENTS

 

Inflammatory disease of the orbit

115

Orbital cellulitis or abscess secondary to tooth root

 

inflammation

115

Orbital inflammation secondary to deep orbital

 

soft tissue injury

117

Penetrating injury from the oral cavity

117

Penetrating injury from external trauma, including

 

bite-wounds

117

Orbital inflammation associated with specific

 

organisms

117

Mycotic infections

117

Bacterial infections

117

Parasitic infestations

117

Canine extraocular polymyositis

120

Masticatory muscle myositis

121

Other, poorly characterized, orbital sclerosing

 

conditions

121

Feline restrictive orbital sarcoma (feline sclerosing

 

pseudotumor)

121

Canine systemic histiocytosis

121

Cystic lesions of the orbit

123

Acquired conjunctival cyst

123

Dermoid cyst

123

Salivary or lacrimal ductular cyst

125

Zygomatic salivary mucocele

125

Vascular lesions of the orbit

126

Orbital fat prolapse (herniation)

126

Neoplastic diseases

126

Lymphoma

126

Soft tissue sarcomas

127

Fibrosarcoma, high grade

127

Morphologically low-grade, biologically high-grade

 

fibrosarcoma of dogs

127

Anaplastic sarcoma

128

Liposarcoma

128

Extraskeletal osteosarcoma

129

Rhabdomyosarcoma

129

Hemangiosarcoma

129

Tumors of the skull, extending to the orbit

129

Osteosarcoma

129

Canine multilobular tumor of bone (chondroma rodens)

131

Feline skeletal osteochondromatosis (multiple cartilaginous

 

exostoses)

131

Other hyperostotic syndromes that may affect the orbit

131

Canine orbital meningioma

131

Salivary or lacrimal gland adenocarcinomas

134

Canine orbital multilobular adenoma

134

Secondary, metastatic neoplasms

138

Diseases of the orbit may originate within the structures of the bony orbit (that vary between species), or in the orbital soft tissues, including the globe, extraocular muscles, and variable secretory tissues such as the zygomatic salivary gland, as well as the rich neurovascular supply to these tissues. However, many diseases affecting the orbit represent the extension of inflammatory or neoplastic processes from adjacent tissues. Thus, important anatomic considerations in the diagnosis of orbital disease also include the proximity of the oral and nasal cavities, the para-nasal sinuses, muscles of mastication, and brain.

INFLAMMATORY DISEASE OF THE ORBIT

Orbital inflammatory disease is relatively common

In the COPLOW collection, orbital inflammation is usually diagnosed in conjunction with panophthalmitis, in globes that were enucleated because of intraocular inflammation that had concurrent orbital inflammation

This combination is most common in dogs and there are 84 cases in the COPLOW collection.

Orbital cellulitis or abscess secondary to tooth root inflammation (Fig. 6.1)

Most common in dogs, rabbits, chinchillas, and horses

Periodontitis extending to the root apex

Pulpitis due to exposure of the root canal from trauma or caries, which occurs less frequently in domestic animal species than in humans

115

Veterinary Ocular Pathology

 

 

Figure 6.1  Orbital abscess. (A) Gross

 

 

photograph of sectioned rabbit skull with

 

 

orbital abscess related to dental disease. (B)

 

 

Golden Retriever, 5 years old: periocular

 

 

swelling and serosanguineous discharge was

 

 

due to a dental abscess. (C) DSH, 8 years old:

 

 

this globe is exophthalmic, the conjunctiva is

 

 

hyperemic and chemotic, and the right side of

 

 

the face is swollen secondary to a dental

 

 

abscess. (D) DSH, 5 years old: the third eyelid is

 

 

hyperemic and prolapsed over the exophthalmic

 

 

globe. Exposure keratitis resulted in poor

 

 

visualization of the anterior segment. (E) Rabbit

 

 

skull radiograph showing periapical bone lysis

 

 

(arrow). (F) Gross photograph of the skull in (E)

 

 

showing abscess extending into the calvarium

A

B

(arrow). (G) Gross photograph of canine globe

 

 

showing an orbital abscess in the posterior pole

 

 

as well as panophthalmitis. (H) Subgross

 

 

photomicrograph of a similar canine globe with

 

 

abscess in the orbital tissues at the posterior

 

 

pole.

C D

E F

G H

116

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