Ординатура / Офтальмология / Английские материалы / Veterinary Ocular Pathology A Comparative Review_Dubielzig, Ketring, McLellan_2010
.pdf
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
107
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
|
|
|
Non-surgical trauma |
Chapter |
|
5 |
|
|
|
|
|
|
|
|
|
||||
|
|
|
|
|
|
|
|
|
|
|
|
|
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
109
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.
110
Non-surgical trauma |
Chapter |
|
|
5 |
|
|
|
|
|
|
|||||
|
|
|
|
|
|
|
|
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. |
111
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 (*).
113
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.
114
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
- #28.03.202621.35 Mб0Uveitis Fundamentals and Clinical Practice 4th edition_Nussenblatt, Whitcup_2010.chm
- #
- #
- #28.03.202627.87 Mб0Vaughan & Asbury's General Ophthalmology 17th edition_Riordan-Eva, Whitcher_2007.chm
- #
- #
- #
- #28.03.202627.2 Mб0Visual Development Diagnosis and Treatment of the Pediatric Patient, 1st edition_Duckman_2006.chm
- #
- #
- #
