• View in gallery
    Figure 1—

    Photograph of the distal portion of the right thoracic limb of a 5-year-old Labrador Retriever that was examined because of a swelling on the dorsal aspect of the metacarpal region (adjacent the carpus) of several months' duration. The owner reported that the swelling developed shortly after the dog sustained an injury to the area. On palpation, the lesion was firmly adhered and hard; mild signs of pain were elicited during manipulation.

  • View in gallery
    Figure 2—

    Photomicrograph (subgross view) of a section of the mass excised from the dog in Figure 1. Notice the distinct cartilage cap, which transitions into bony trabeculae that are continuous with the marrow cavity of the underlying bone (not shown). H&E stain; bar = 1 cm.

  • View in gallery
    Figure 3—

    Photomicrograph of a section of the mass excised from the dog in Figure 1. Trabeculae of cartilage (arrow) have an orderly pattern of mineralization and ossification (arrowhead) and transition into mature trabecular bone (star). Intertrabecular spaces contain loose, paucicellular, variably myxoid tissue and abundant congested small-caliber, thin-walled vessels. H&E stain; bar = 150 μm.

  • View in gallery
    Figure 4—

    Photomicrograph of a section of the mass excised from the dog in Figure 1. In this view, there is evidence of active remodeling of the bony trabeculae, including basophilic reversal lines (arrowhead), osteoclasts within resorption bays (arrow), and multifocal lining by a single layer of plump osteoblasts (star). H&E stain; bar = 50 μm.

  • 1.

    Thompson KG, Poole RR. Tumors in domestic animals. 4th ed. Ames, Iowa: Iowa State Press, 2002;256259.

  • 2.

    Owen LN, Bostock DE. Multiple cartilaginous exostoses with development of a metastasizing osteosarcoma in a Shetland Sheepdog. J Small Anim Pract 1971;12:507512.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 3.

    Porter DE, Simpson AH. The neoplastic pathogenesis of solitary and multiple osteochondromas. J Pathol 1999;188:119125.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 4.

    Thompson K. Jubb, Kennedy and Palmer's pathology of domestic animals. 5th ed. Edinburgh: Elsevier, 2007;9,119.

  • 5.

    Shupe JL, Leone NC & Olson AE, et al. Hereditary multiple exostoses: clinicopathologic features of a comparative study in horses and man. Am J Vet Res 1979;40:751757.

    • Search Google Scholar
    • Export Citation
  • 6.

    Caporn TM, Read RA. Osteochondromatosis of the cervical spine causing compressive myelopathy in a dog. J Small Anim Pract 1996;37:133137.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 7.

    Ness MG. Osteochondroma causing progressive posterior paresis in a Lakeland Terrier puppy. Vet Rec 1993;132:608609.

  • 8.

    Santen DR, Payne JT & Pace LW, et al. Thoracolumbar vertebral osteochondroma in a young dog. J Am Vet Med Assoc 1991;199:10541056.

  • 9.

    Chester DK. Multiple cartilaginous exostoses in two generations of dogs. J Am Vet Med Assoc 1971;159:895897.

  • 10.

    Poole RR, Carrig CB. Multiple cartilaginous exostoses in a cat. Vet Pathol 1972;9:350359.

  • 11.

    Mintzer CM, Klein JD, Kasser JR. Osteochondroma formation after a Salter II fracture. J Orthop Trauma 1994;8:437439.

  • 12.

    Bates DL, Osborne WM. Post-traumatic osteochondroma of the calcaneus. J Am Podiatr Med Assoc 1990;80:606607.

  • 13.

    Cohen AP, Giannoudis PV & Hinsche A, et al. Post-traumatic giant intraarticular synovial osteochondroma of the knee. Injury 2001;32:8789.

  • 14.

    Scoggin JF III, Jacques KM. Post-traumatic osteochondroma formation following intramedullary fracture fixation. Orthopedics 2001;24:991992.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 15.

    Taitz J, Cohn RJ & White L, et al. Osteochondroma after total body irradiation: an age-related complication. Pediatr Blood Cancer 2004;42:225229.

  • 16.

    Harper GD, Dicks-Mireaux C, Leiper AD. Total body irradiation-induced osteochondromata. J Pediatr Orthop 1998;18:356358.

  • 17.

    Rosenberg A. Robbins and Cotran pathologic basis of disease. 7th ed. Philadelphia: Elsevier Saunders, 2005;1296.

Advertisement

Pathology in Practice

Jennifer W. KoehlerDepartment of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL 36849.

Search for other papers by Jennifer W. Koehler in
Current site
Google Scholar
PubMed
Close
 DVM
,
Calvin M. JohnsonDepartment of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL 36849.

Search for other papers by Calvin M. Johnson in
Current site
Google Scholar
PubMed
Close
 DVM, PhD, DACVP
,
Debra M. BeardDepartment of Clinical Sciences, College of Veterinary Medicine, Auburn University, Auburn, AL 36849.

Search for other papers by Debra M. Beard in
Current site
Google Scholar
PubMed
Close
 DVM, MS, DACVR
, and
L. Nicki GreenDepartment of Clinical Sciences, College of Veterinary Medicine, Auburn University, Auburn, AL 36849.

Search for other papers by L. Nicki Green in
Current site
Google Scholar
PubMed
Close
 DVM
View More View Less

History

A 5-year-old ovariohysterectomized female Labrador Retriever was evaluated because of a swelling on the dorsal aspect of the right metacarpal region of several months' duration. The owner reported that the swelling developed shortly after the dog injured the area by falling through a sea wall at a beach and that since that time, the dog had signs of pain and lameness for several days after it was highly active or sustained any minor trauma to the affected area.

Clinical and Gross Findings

At the time of the evaluation, the dog was bright, alert, and responsive. A hard mass (4 cm in diameter) was firmly adhered to the dorsal aspect of the proximal portion of the right metacarpal region adjacent to the carpal joint (Figure 1). Mild signs of pain were elicited during manipulation of the mass. No other physical abnormalities were present. Radiography revealed a well-circumscribed, smoothly marginated, inhomogeneous bone opacity that was adhered to and protruding from the proximal portion of the third metacarpal bone. Mild bony proliferation was associated with the third carpal bone. The dog was anesthetized for surgery, and the mass was excised and submitted for histologic examination.

Figure 1—
Figure 1—

Photograph of the distal portion of the right thoracic limb of a 5-year-old Labrador Retriever that was examined because of a swelling on the dorsal aspect of the metacarpal region (adjacent the carpus) of several months' duration. The owner reported that the swelling developed shortly after the dog sustained an injury to the area. On palpation, the lesion was firmly adhered and hard; mild signs of pain were elicited during manipulation.

Citation: Journal of the American Veterinary Medical Association 237, 1; 10.2460/javma.237.1.45

Formulate differential diagnoses from the history, clinical findings, and Figure 1—then turn the page

Histopathologic Findings

Histologic examination of tissue sections revealed a well-delineated, nonencapsulated, multilobulated mass with a 1- to 2-mm-thick, well-defined, continuous, irregular, apical cap of mildly dysplastic hyaline cartilage, which had an orderly pattern of mineralization and transition into mature trabecular bone toward the central and deeper areas of the mass (Figures 2 and 3). Bony trabeculae were slightly irregular in shape and distribution, with wide intertrabecular spaces that contained loose, myxoid tissue or more cellular streams of spindle-shaped cells that resembled fibroblasts. Within these spaces, abundant congested, thin-walled blood vessels with multifocal vascular disruption and perivascular hemorrhage were evident. Bony trabeculae appeared to have been undergoing active remodeling as evidenced by basophilic reversal lines (ie, basophilic cement lines that are wavy rather than smooth and are an indication that the previous cellular activity at the site was resorptive), trabeculae that were multifocally lined by a single layer of plump osteoblasts, and scattered osteoclasts within resorption bays (Figure 4). The dorsal surface of the mass had a thin, overlying band of compressed dermal collagen and extended to all surgical margins.

Figure 2—
Figure 2—

Photomicrograph (subgross view) of a section of the mass excised from the dog in Figure 1. Notice the distinct cartilage cap, which transitions into bony trabeculae that are continuous with the marrow cavity of the underlying bone (not shown). H&E stain; bar = 1 cm.

Citation: Journal of the American Veterinary Medical Association 237, 1; 10.2460/javma.237.1.45

Figure 3—
Figure 3—

Photomicrograph of a section of the mass excised from the dog in Figure 1. Trabeculae of cartilage (arrow) have an orderly pattern of mineralization and ossification (arrowhead) and transition into mature trabecular bone (star). Intertrabecular spaces contain loose, paucicellular, variably myxoid tissue and abundant congested small-caliber, thin-walled vessels. H&E stain; bar = 150 μm.

Citation: Journal of the American Veterinary Medical Association 237, 1; 10.2460/javma.237.1.45

Figure 4—
Figure 4—

Photomicrograph of a section of the mass excised from the dog in Figure 1. In this view, there is evidence of active remodeling of the bony trabeculae, including basophilic reversal lines (arrowhead), osteoclasts within resorption bays (arrow), and multifocal lining by a single layer of plump osteoblasts (star). H&E stain; bar = 50 μm.

Citation: Journal of the American Veterinary Medical Association 237, 1; 10.2460/javma.237.1.45

Morphologic Diagnosis

Osteochondroma.

Comments

On the basis of radiographic findings, the differential diagnoses for the dog of this report included periosteal reaction secondary to lick granuloma, multiple cartilaginous exostoses, or neoplasia (including osteochondroma and parosteal or other osteosarcoma). Histologic findings confirmed that the mass was an osteochondroma. Osteochondromas are benign, cartilage-capped, tumor-like exostoses that arise from the surfaces of endochondral bones.1 They can be monostotic (involving 1 bone) or polyostotic (involving multiple bones). The marrow cavity of these growths is continuous with the marrow cavity of the bone of origin, making them morphologically more suggestive of a dysplastic, rather than neoplastic, process. Nevertheless, malignant transformation within long-standing polyostotic lesions can occur, although malignant transformation within monostotic lesions has only been detected in humans.1–3 In veterinary medicine, the polyostotic form is more common and has been detected in mature cats as well as young dogs and horses; the age of onset, affected bone, and location along the bone vary depending on the species.1,4 In horses, the lesions may be present at birth and are often bilaterally symmetric.5 In dogs, the lesions are not present at birth but develop in juvenile animals and enlarge in conjunction with skeletal growth.1 Common sites of osteochondromas in horses and dogs include the metaphyses of long bones, pelvis, ribs, scapulae, and vertebrae.1 Most lesions are of little clinical consequence, but vertebral lesions can occasionally impinge upon the spinal cord and cause considerable morbidity.6–8 The disease characteristics of osteochondromatosis in cats differ somewhat from those in affected horses and dogs, in that lesions develop in mature cats and primarily involve flat bones (including bones of the skull that are formed via intramembranous ossification).1,4 In horses and dogs, the disease is inherited as an autosomal dominant trait, as it is in humans.1,4,5,9 In cats, the etiology is less clear. Because the lesions in cats are slightly different in microscopic appearance (ie, the marrow cavity is not continuous with the bone of origin), compared with findings in the other 2 species, it is likely that the condition in cats is not analogous to that in horses or dogs.10 Feline leukemia virus particles have been identified within lesions, but the importance and causality of this finding have not been fully elucidated.4

Monostotic, solitary, osteochondromas that develop in humans following trauma11–14 or whole-body irradiation15,16 have been reported. To the authors' knowledge, no case report of confirmed post-traumatic monostotic osteochondroma in a dog has been published. Debate continues as to whether these lesions represent a neoplastic or simply a dysplastic process. In humans, inactivation of both copies of the EXT gene in growth plate chondrocytes has been implicated in the pathogenesis of both sporadic and hereditary osteochondromas,17 but this has not been investigated in veterinary patients. The argument for development of post-traumatic monostotic lesions as a result of a dysplastic process is, however, particularly compelling. Experimentally, osteochondromas can develop following transplantation of fragments of physeal growth plate to the periosteal surface.1 In the dog of this report, the proximity of the lesion to the physis of the affected bone and the known history of trauma to the area further supported the diagnosis of post-traumatic monostotic osteochondroma.

References

  • 1.

    Thompson KG, Poole RR. Tumors in domestic animals. 4th ed. Ames, Iowa: Iowa State Press, 2002;256259.

  • 2.

    Owen LN, Bostock DE. Multiple cartilaginous exostoses with development of a metastasizing osteosarcoma in a Shetland Sheepdog. J Small Anim Pract 1971;12:507512.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 3.

    Porter DE, Simpson AH. The neoplastic pathogenesis of solitary and multiple osteochondromas. J Pathol 1999;188:119125.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 4.

    Thompson K. Jubb, Kennedy and Palmer's pathology of domestic animals. 5th ed. Edinburgh: Elsevier, 2007;9,119.

  • 5.

    Shupe JL, Leone NC & Olson AE, et al. Hereditary multiple exostoses: clinicopathologic features of a comparative study in horses and man. Am J Vet Res 1979;40:751757.

    • Search Google Scholar
    • Export Citation
  • 6.

    Caporn TM, Read RA. Osteochondromatosis of the cervical spine causing compressive myelopathy in a dog. J Small Anim Pract 1996;37:133137.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 7.

    Ness MG. Osteochondroma causing progressive posterior paresis in a Lakeland Terrier puppy. Vet Rec 1993;132:608609.

  • 8.

    Santen DR, Payne JT & Pace LW, et al. Thoracolumbar vertebral osteochondroma in a young dog. J Am Vet Med Assoc 1991;199:10541056.

  • 9.

    Chester DK. Multiple cartilaginous exostoses in two generations of dogs. J Am Vet Med Assoc 1971;159:895897.

  • 10.

    Poole RR, Carrig CB. Multiple cartilaginous exostoses in a cat. Vet Pathol 1972;9:350359.

  • 11.

    Mintzer CM, Klein JD, Kasser JR. Osteochondroma formation after a Salter II fracture. J Orthop Trauma 1994;8:437439.

  • 12.

    Bates DL, Osborne WM. Post-traumatic osteochondroma of the calcaneus. J Am Podiatr Med Assoc 1990;80:606607.

  • 13.

    Cohen AP, Giannoudis PV & Hinsche A, et al. Post-traumatic giant intraarticular synovial osteochondroma of the knee. Injury 2001;32:8789.

  • 14.

    Scoggin JF III, Jacques KM. Post-traumatic osteochondroma formation following intramedullary fracture fixation. Orthopedics 2001;24:991992.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 15.

    Taitz J, Cohn RJ & White L, et al. Osteochondroma after total body irradiation: an age-related complication. Pediatr Blood Cancer 2004;42:225229.

  • 16.

    Harper GD, Dicks-Mireaux C, Leiper AD. Total body irradiation-induced osteochondromata. J Pediatr Orthop 1998;18:356358.

  • 17.

    Rosenberg A. Robbins and Cotran pathologic basis of disease. 7th ed. Philadelphia: Elsevier Saunders, 2005;1296.

Contributor Notes

Dr. Beard's present address is Veterinary Diagnostic Imaging of Auburn, PO Box 108, Auburn, AL 36831.

Dr. Green's present address is Veterinary Surgery Center, 13551 N Indiana Ave, Oklahoma City, OK 73134.

Address correspondence to Dr. Koehler (jaw0007@auburn.edu).