Vet Comp Orthop Traumatol 2005; 18(02): 100-104
DOI: 10.1055/s-0038-1632938
Case Report
Schattauer GmbH

Transient benign osteopetrosis in a calf persistently infected with bovine virus diarrhoea virus

K. Nuss
1   Clinic for Surgery
,
A. Spiess
1   Clinic for Surgery
,
M. Hilbe
4   Institute for Veterinary Pathology, Vetsuisse-Faculty, University of Zurich, Switzerland
,
K. Sterr
2   Institute of Pathology, Veterinary Faculty of the Ludwig-Maximilians-University of Munich, Germany
,
M. Reiser
3   Department of Radiology, University of Munich, Germany
,
U. Matis
1   Clinic for Surgery
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Received 18. April 2004

Accepted 16. Juni 2004

Publikationsdatum:
08. Februar 2018 (online)

Summary

A two-day-old Simmental calf was admitted suffering from a fracture of the right femur. The radiographs showed striking changes in all bones, evident as alternating zones of dense and less dense tissue (bone-inbone) in the right femur and striped densities in the vertebral bodies. A stainless steel plate was used to repair the fracture, which healed well. The calf developed normally but was diagnosed as persistently infected with bovine virus diarrhoea (BVD) virus. It was kept in isolation and examined physically and radiographically during the following 13 months. The radiographic changes diminished during the first three months and at 13 months were barely visible. The animal was euthanatized, and immunohistochemistry revealed BVD virus antigen in numerous tissues. The radiographic abnormalities seen in this case are similar to those of the transient form of osteopetrosis in humans. Osteopetrosis in humans is currently thought to have a genetical cause, whereas it appears to be associated with viral disease in animals.

 
  • References

  • 1 Albers-Schönberg H. Eine bisher nicht beschriebene Allgemeinerkrankung des Skelettes im Röntgenbild. Fortschritte auf dem Gebiet der Röntgenstrahlen 1907; 11: 261-3.
  • 2 Zawisch C. Marble bone disease. A study of osteogenesis. Arch Pathol 1947; 43: 55-76.
  • 3 Umemura T. et al. Persistence of secondary spongiosa in three calves. VetPathol 1988; 25: 312-4.
  • 4 Weisbrode S. et al. Bone and Joints. In: Thomson s Special Veterinary Pathology. McGavin M, Carlton W, Zachary J. (eds) St. Louis: Mosby; 2001: 499-536.
  • 5 Greene H. et al. Congenital osteopetrosis in Angus calves. J Am Vet Med Assoc 1974; 164 (4) 389-95.
  • 6 Riser W. et al. Osteopetrosis in the dog: a report of three cases. J AmVet Radiol Soc 1970; 11: 29-34.
  • 7 Helfrich M. et al. Morphologic features ofbone in human osteopetrosis. Bone 1991; 12: 411-9.
  • 8 Revell PA. Pathology of bone. Berlin: Springer; 1986
  • 9 Horton W. et al. Osteopetrosis. Further heterogeneity Pediatrics 1980; 97: 580.
  • 10 El-Tawil T. et al. Benign osteopetrosis: a review of 42 cases showing two different patterns. Skeletal Radiol 1993; 22: 587-93.
  • 11 Benichou Oetal. Further evidence for genetic heterogeneity with type II autosomal dominant osteopetrosis. J Bone Miner Res 2000; 15 (10) 1900-4.
  • 12 Cleiren E. et al. Albers-Schönberg-disease (autosomal dominant osteopetrosis, type II) results from mutations in the CICN7 chloride channel gene. Hum Mol Genet 2001; 10 (25) 2861-7.
  • 13 Yousheng X. et al. Radiologic manifestations of osteopetrosis. Chin Med J 1995; 108 (9) 692-298.
  • 14 Monaghan B. et al. Transient infantile osteopetrosis. J Pediatr 1991; 118: 252-6.
  • 15 McCune D. et al. Osteopetrosis (marble bones) in an infant. Review of the literature and report of a case. Am J Dis Child 1934; 48: 949-1000.
  • 16 Goedegebuure S. et al. Kongenitale Osteopetrosis bei zwei Kälbern und einem Schaf. Zentralblatt für Veterinärmedizin A 1981; 28: 345-56.
  • 17 Nägele M. et al. Osteopetrose-Albers-Schönberg-Erkrankung unter Berücksichtigung kernspinto-mographischer Befunde. Fortschritte Röntgenstrahlen 1987; 147 (6) 687-9.
  • 18 Müller-Stephan H. Osteosynthese bei Marmorknochenkrankheit Albers-Schönberg. Beitr Orthop Traumatol 1968; 15 (10) 639-40.
  • 19 Windholz F. Osteosclerosis fragilis generalisata (Marmorknochenkrankheit) mit periostaler Knochenneubildung. Zeitschrift für Kinderheilkunde 1931; 51: 708-28.
  • 20 Engfeldt B. et al. Sudies on osteopetrosis. Acta Paediatrica 1960; 49: 391-408.
  • 21 Leipold H. et al. Animal Model of human disease. Osteopetrosis in Angus and Hereford Calves. Am J Pathol 1977; 86 (3) 745-8.
  • 22 Hirsbrunner G. et al. Was diagnostizieren Sie?. Schweizer Archiv für Tierheilkunde 1998; 140: 114-6.
  • 23 Hilbe M. et al. Abnormal bone development associated with bovine virus diarrhea virus (BVDV) infection in anewborn calf. Eur J Vet Pathol 2000; 6 (3) 115-9.
  • 24 Bielefeldt-Ohmann H. et al. Demonstration of bovine viral diarrhoea virus in peripheral blood mononuclear cells of persistently infected, clinically normal cattle. J Gen Virol 1987; 68: 1971-982.
  • 25 Spagnuolo MS. et al. Bovine Viral Diarrhoea Virus infection in bone marrow of experimentally infected calves. J Comp Pathol 1997; 116: 97-100.
  • 26 Scruggs D. et al. Osteopetrosis, anemia, thrombocytopenia, and marrow necrosis in beef calves naturally infected with bovine virus diarrhea virus. J Vet Diagn Invest 1995; 7: 555-9.
  • 27 Potgieter L. Bovine respiratory tract disease caused by bovine viral diarrhea virus. Vet Clin NorthAmFoodAnimPract 1997; 13 (3) 471-81.
  • 28 Ellis JA. The immunology of the bovine respiratory disease complex. Vet Clin North Am Food Anim Pract 2001; 17 (3) 535-50.
  • 29 Gibbons D. et al. Pathogenicity of the border disease agent for the bovine fetus. Br Vet J 1974; 130: 357-61.
  • 30 Nettleton P. et al. Ruminant pestiviruses. Br Vet J 1995; 151: 615-42.
  • 31 Taylor LF. et al. Performance, survival, necropsy and virological findings from calves persistently infected with the bovine viral diarrhea virus originating from a single Saskatchewan beef herd. Can Vet J 1997; 38: 29-37.
  • 32 Radostits O. et al. Veterinary Medicine. Philadelphia: Saunders; 2000
  • 33 Jubb K, Kennedy PC, Palmer N. (eds) Pathology of domestic animals. San Diego, California: Academic Press; 1992
  • 34 Milhaud G. et al. Thymus and osteopetrosis. Clin Orthop 1978; 114: 31-45.
  • 35 Murray A. et al. Retrovirus-induced osteopetrosis in mice. Ultrastructural evidence of early virus production in osteoblasts and osteocytes. Am J Pathol 1986; 124 (2) 319-23.
  • 36 Labat M. Albers-Schönberg-Disease (osteopetrosis): From developmental disease ofbone to a pre T-cell leukaemia syndrome involving a new retrovirus. Cells and Materials 1991; 1 (Suppl) 59-68.
  • 37 Labat M. Retroviruses and bone diseases. Clin Orthop 1996; 326: 287-309.
  • 38 Kramers P. et al. Osteopetrosis in cats. J Small Anim Pract 1988; 29: 153-64.
  • 39 Mills B. et al. Osteoclasts in human osteopetrosis contain viral-nucleocapsid-like inclusions. J Bone Miner Res 1988; 3: 101-6.
  • 40 Calnek B, Barnes H, Beard C, McDougald L, Saif Y. (eds) Diseases of Poultry. 10 ed. Iowa: Iowa State University Press; 1997
  • 41 Kuramochi T. et al. Histomorphologic observation of avian leukosis virus infection and avian osteopetrosis in chicken. In: www.sicot.org/abstracts/Paris/abstract54.html editor 2001 August 29-September 1 Paris: The International Society of Orthopaedic Surgery and Traumatology; 2001. p. Abstract 54.
  • 42 Potts B. et al. Possible role of pestiviruses in microcephaly. Lancet 1987; 1 (8539) 972-3.
  • 43 Wilks C. et al. Bovine pestivirus and human infection. Lancet. 1989 1. (8629) 107.
  • 44 Thür B. et al. Immunhistologie als zuverlässige und effiziente Methode für die Diagnose von BVD-Infektionen. Schweizer Archiv für Tierheilkunde 1996; 138: 476-82.
  • 45 Constable P. et al. Femoral and tibial fractures in a newborn calf after transplacental infection with bovine viral diarrhoea virus. Vet Rec 1993; 132 (April 10) 383-5.