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Massive Osteolysis in Association with Multiple Cerebrospinal Fluid Fistulae

Published online by Cambridge University Press:  18 September 2015

Harold J. Hoffman ,
Derek C. Harwood-Nash ,
T. P. Morley  and
N. Barry Rewcastle
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A female child, TK, was born January 12, 1965, and was initially admitted to the Hospital for Sick Children, Toronto, on January 13, 1972, at age seven years with a sevenday history of runny nose, earache, headache, and fever. On the day before admission, she had a grand mal seizure and lumbar puncture revealed purulent cerebrospinal fluid (C.S.F.) which grew pneumococci. She was treated with antibiotics, her meningitis resolved, and she was discharged home nine days after admission.

Type
University of Toronto Neurosurgical Rounds No. 1
Information
Canadian Journal of Neurological Sciences , Volume 7 , Issue 1 , February 1980 , pp. 39 - 44
Copyright
Copyright © Canadian Neurological Sciences Federation 1980

References

REFERENCES

Aston, J. N. (1958). A case of massive osteolysis of the femur, J. Bone Joint Surg., 40B, 514.CrossRefGoogle Scholar
Bickel, W.H. and Broders, A.C. (1947). Primary lymphangioma of ilium. Report ofa Case, J. Bone and Joint Surg., 29, 517.Google ScholarPubMed
Branco, F. and Dasilva, H.J. (1958). Notes on a rare case of essential osteolysis, J. Bone Joint Surg., 40B, 519.CrossRefGoogle ScholarPubMed
Caulet, T., Fandre, M., Adnet, J.J., Coffin, R.. Pennaforte, F. and Mathey, J. (1968). Osteolyse massive scapulo-cleido-costale. Étude histoche-mique et ultrastructurale, Ann. d’Anat. Path., 13, 177.Google Scholar
Fornasier, V. L. (1970). Hemangiomatosis with massive osteolysis, J. Bone Joint Surg., 53B, 444.CrossRefGoogle ScholarPubMed
Gorham, L.W., Wright, A.W., Shultz, H.H. and Maxon, F.C. JR. (1954). Disappearing Bones: A rare form of massive osteolysis. Report of two cases, one with autopsy findings. Am. J. Med., 17, 674–682.CrossRefGoogle Scholar
Gorham, L.W. and Stout, A.P. (1955). Massive osteolysis, J. Bone Joint Surg., 37A, 985.CrossRefGoogle ScholarPubMed
Gorham, L.W. (1966). Circulatory changes associated with osteolytic and osteoblastic reactions. Arch. Int. Med., 105, 199.CrossRefGoogle Scholar
Halliday, D R., Dahlin, D C, Pugh, D.G. and Young, H.H. (1964). Massive osteolysis and angiomatosis, Radiology, 82, 637–644.CrossRefGoogle ScholarPubMed
Heyden, G., Kindblom, L.G. and Nielsen, J. M. (1977). Disappearing bone disease, J. Bone Joint Surg., 59A, 57–61.CrossRefGoogle ScholarPubMed
Jackson, J.B.S. (1838). A singular case of absorption of bone (a boneless arm), Boston Med. Surg. J., 18, 368.Google Scholar
Jacobs, J.E. and Kimmelstiel, P. (1953). Cystic angiomatosis of the skeletal system, J. Bone Joint Surg., 35A, 409.CrossRefGoogle ScholarPubMed
Johnson, P.M. and McClure, J.G. (1958). Observations on massive osteolysis. Radiology, 71, 28.CrossRefGoogle ScholarPubMed
King, D.J. (1946). Case resembling hemangiomatosis of the lower extremity, J. Bone Joint Surg., 28, 623.Google ScholarPubMed
Lichtenstein, L. (1965). Bone tumours, Louis, St., The C.V. Mosby Co.Google Scholar
Reiley, B.J., Davidson, J.W., Bain, H. (1972), Lymphangiectasis of the skeleton — a case report, Radiology, 103, 385.CrossRefGoogle Scholar
Ross, J.L., Schinella, R. and Shenkman, L. (1978). Massive osteolysis. An unusual cause of bone destruction, Am. J. of Med., 65, 367–372.CrossRefGoogle ScholarPubMed
Sage, M.R., Allen, P.W. (1974). Massive osteolysis, J. Bone Joint Surg., 56B, 130.Google ScholarPubMed
Sherman, M.W. (1944). Capillary hemangioma of bone, Arch. Path., 38, 158.Google Scholar
Thompson, J.W. and Schurman, D.J. (1974). Massive osteolysis, Clin. Orthop., 103, 206.CrossRefGoogle Scholar