Numerous bleeding episodes, neurological signs and symptoms, and pulmonary arteriovenous malformations are well documented in reports of families with hereditary hemorrhagic telangiectasia. It is always assumed that these are due to the arteriovenous malformations. We are here reporting a case with positive cerebral angiographic findings of large arteriovenous communications, as well as catheterization data revealing pulmonary ab normalities secondary to the cerebral arteriovenous fistula, but no ab normalities within the pulmonary vasculature itself.
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References
1.
Carpenter, S. , and Schumacher, G.A.: Familial infantile cerebellar atrophy associated with retinal degeneration. Arch. Neurol.14: 82, 1966.
2.
McCormick, W.F. : The pathology of vascular ("arteriovenous") malformations. J. Neurosurg.24: 807, 1966.
3.
Russell, D.S., and Rubinstein, L.J. : Pathology of Tumours of the Nervous System , 2nd ed. Baltimore, The Williams and Wilkins Co., 1963.
4.
Slager, U.T.: Basic Neuropathology. Baltimore, The Williams and Wilkins Co., 1970.
5.
Dolowitz, D.A. , Rambo, O.N., and Stephens , F.E.: Hereditary hemorrhagic telangiectasis. Ann. Otol. Rhinol. Laryngol.62: 642, 1953.
6.
Tobin, J.R., and Wilder, T.C.: Pulmonary arteriovenous fistula associated with hereditary hemorrhagic telangiectasis: a report of their occurrence in a father and son. Ann. Intern. Med.38: 868, 1953.
7.
Harrison, T.R., Adams, R.D., Bennett, 1. L., Jr., Resnik, W. H., Thorn, G. W., and Wintrobe, M. M.: Principles of Internal Medicine . New York, McGraw-Hill Book Co. , 1966.
Bormon, J.B. , and Schiller, M.: Osler's disease with multiple large vessel aneurysms. Angiology20: 113, 1969.
14.
Bird, R.M., and Jaques, W.E.: Vascular lesion of hereditary hemorrhagic telangiectasis. N. Engl. J. Med.260: 597, 1959.
15.
Hodgson, C.H. , Burchell, H.B., Good , C.A., et al.: Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous fistula. N. Engl. J. Med.261: 625, 1959.
16.
Osler, W.: On multiple hereditary telangiectases with recurring hemorrhages. Q. J. Med.1: 53, 1907.
17.
—: On family form of recurring epistaxis, associated with multiple telangiectases of skin and mucous membranes. Bull. Johns Hopkins Hosp.12: 333, 1901.
18.
Rendu: Epistaxis répétées: chez un sujet porteur de petits angiomes cutanés et musqueux. Bull. et Mém. Soc. Méd. d Hôp. de Paris.13: 731, 1896.
19.
Weber, F.P. : Multiple hereditary developmental angiomata (telangiectases) of skin and mucous membranes associated with recurring hemorrhages . Lancet2: 160, 1907.