Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 14-Day Trial for You and Your Team.

Learn More →

HEREDITARY HEMORRHAGIC TELANGIECTASIA (OSLER'S DISEASE): A REVIEW OF THE LITERATURE AND REPORT OF CASES

HEREDITARY HEMORRHAGIC TELANGIECTASIA (OSLER'S DISEASE): A REVIEW OF THE LITERATURE AND REPORT OF... Abstract Hereditary hemorrhagic telangiectasia is a rare disease, probably due to mesenchymal dysplasia. It is characterized by the presence of multiple acquired angiomas or telangiectases of varying distribution and number with a marked tendency to bleed spontaneously or from slight trauma. The disease is not sex bound. It is transmitted as a dominant characteristic. The initial symptom usually consists of abnormally profuse epistaxis beginning about puberty. This is followed by the development of multiple telangiectasia of the skin and mucous membranes from the age of 25 to 35. Hemorrhage from the nasal mucosa is most frequent, and all symptoms tend to reach their greatest severity during the fourth decade. The average mortality rate is 4 per cent. The lesions are most commonly found in the nasal mucosa, the skin of the face, the buccal mucosa, the lips, the tongue, the floor of the mouth, the scalp, the ears, the conjunctivas and References 1. Houser, K. M.: Hereditary Hemorrhagic Telangiectasia , Ann. Otol., Rhin. & Laryng. 43:731-738 ( (Sept.) ) 1934. 2. Aubertin, C.; Levy, R., and Baclesse: L'angiomatose hemorragique familiale (maladie de Rendu-Osler) , Presse méd. 41:185-188 ( (Feb.) ) 1933. 3. Teahan, W. W.: Hereditary Hemorrhagic Telangiectasia Occurring in Six Generations , Ann. Int. Med. 13:535-543 ( (Sept.) ) 1939. 4. Alban, H.: Hereditary Hemorrhagic Telangiectasia , Northwest Med. 40:86-88 ( (March) ) 1941. 5. Goldstein, H. I.: Goldstein's Heredofamilial Angiomatosis with Recurring Familial Hemorrhage (Rendu-Osler-Weber's Disease) , Arch. Int. Med. 58:836-865 ( (Nov.) ) 1931. 6. Fingerland, A., and Janousek, B.: Hereditary Hemorrhagic Telangiectasia (Osler's Disease) , Arch. f. Dermat. u. Syph. 178:54-64, 1938. 7. Figi, F. A., and Watkins, C. H.: Hereditary Hemorrhagic Telangiectasia , Ann. Otol., Rhin. & Laryng. 52:330-341 ( (June) ) 1943. 8. Goldstein, H. I.: Hereditary Multiple Telangiectasia , Arch. Dermat. & Syph. 26:282-308 ( (Aug.) ) 1932. 9. Ullmann, K.: Angiomatosis (K. Ullmann) and Osler's Disease , Urol. & Cutan. Rev. 37:619-629 ( (Sept.) ) 1933. 10. Kufs, H.: Heredofamilial Angiomatosis of the Brain and Retina and Its Relationship to Skin Angiomatosis , Ztschr. f. d. ges. Neurol. u. Psychiat. 113:651-686, 1928. 11. Junius, P.: Relationship Between Angiomatosis of the Retina, Exudative Retinitis (Coat's) and Osler's Disease , Ztschr. f. Augenh. 84:193-210 ( (Oct.) ) 1934. 12. Michael, J. C., and Levin, P. M.: Multiple Telangiectases of the Brain: A Discussion of Hereditary Factors in Their Development , Arch. Neurol. & Psychiat. 36:514-529 ( (Sept.) ) 1936. 13. Ironside, R., and Hill, D.: Cutaneous Naevus with Buphthalmos and Epilepsy , J. Ment. Sc. 87:631-634 ( (Oct.) ) 1941. 14. Louis-Bar: Progressive Syndrome Consisting of Symmetric Cutaneous and Conjunctival Telangiectases and Cerebellar Manifestations , abstracted, Arch. Dermat. & Syph. 46:890 ( (Dec.) ) 1942. 15. Cordes, F. C., and Hogan, M. J.: Angiomatosis Retinae (Hippel's Disease) , Arch. Ophth. 23:253-269 ( (Feb.) ) 1940. 16. Madden, J. F.: Generalized Angiomatosis (Telangiectasia) , J. A. M. A. 102:442-448 ( (Feb. 10) ) 1934. 17. Muende, I.: Multiple Symmetrical Fibro-Angiomatous Nevi of the Face and Hands , Proc. Roy. Soc. Med. 27:292 ( (Jan.) ) 1934. 18. Goldstein, H. I.: Heredofamilial Angiomatosis (Telangiectasia) with Recurring Hemorrhages , Internat. Clin. 2:43-56 ( (June) ) 1934. 19. Kosiner, R.: Hereditary Hemorrhagic Telangiectasia , Klin. Wchnschr. 14:713-714 ( (May 18) ) 1935. 20. Netherton, E. W., and Curtis, G. H.: Raynaud's Disease with Subcutaneous Calcium Deposition in the Fingers and Hereditary Multiple Telangiectases , Arch. Dermat. & Syph. 46:579-580 ( (Oct.) ) 1942. 21. Kugelmass, I. N.: Hereditary Hemorrhagic Telangiectasis , J. A. M. A. 102:287-291 ( (Jan. 27) ) 1934.Crossref 22. Milbradt, W.: Atypical Diffuse Scleroderma with Osler Syndrome and Hepatic Dysfunction , Dermat. Wchnschr. 99:973-979 ( (July 28) ) 1934. 23. Harding, G.: Ein Fall von Morbus Osler , Acta med. Scandinav. 106:352-368, 1941.Crossref 24. van Bogaert, L.: Two Cases of Hereditary Hemorrhagic Angiomatosis with Hepatosplenomegaly and Two Cases of Hemorrhagic Telangiectasis in Same Family , Bull. et mém. Soc. méd. d. hôp. de Paris 49:1572-1578 ( (Dec. 25) ) 1933. 25. Davis, E.: Hereditary Familial Purpura Simplex , Lancet 2:1110-1114 ( (Nov. 25) ) 1939.Crossref 26. Bankoff, G.: Pathology and Therapy of Essential Telangiectases , München. med. Wchnschr. 80:2035-2037 ( (Dec. 29) ) 1933. 27. Combes, F. C.: Multiple Hereditary Telangiectasia (Osler's Disease) and Cardiovascular Syphilis , Arch. Dermat. & Syph. 44:114-115 ( (July) ) 1941. 28. Michelson, H. E.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 36:241 ( (July) ) 1937. 29. Obermayer, M. E., and Becker, S. W.: Generalized Telangiectasis , Arch. Dermat. & Syph. 43:1077 ( (June) ) 1941. 30. Becker, S. W., and Obermayer, M. E.: Telangiectasia Hemorrhagica Hereditaria (Osler's Disease) and Vitiligo , Arch. Dermat. & Syph. 44:303-304 ( (Aug.) ) 1941. 31. Zeisler, E. P.: Telangiectasia Associated with Syphilis and Pregnancy , Arch. Dermat. & Syph. 5:781 ( (June) ) 1922. 32. McDonough, F. E.; Dry, T. J., and Roth, G. M.: Hereditary Telangiectasia with Visceral Involvement: Special Studies of Skin Temperature; Report of a Case , Proc. Staff Meet., Mayo Clin. 15:593-604 ( (Sept. 18) ) 1940. 33. Renshaw, J. F.: Multiple Hemorrhagic Telangiectasia with Special Reference to Gastroscopic Appearance , Cleveland Clin. Quart. 6:226-230 ( (July) ) 1939. 34. Griggs, D. E., and Baker, M. Q.: Hereditary Hemorrhagic Telangiectasia with Gastro-Intestinal Bleeding , Am. J. Digest. Dis. 8:344-346 ( (Sept.) ) 1941. 35. Stellar, L. I.: Hereditary Telangiectasia: Report of a Case , New England J. Med. 226:336-338 ( (Feb. 26) ) 1942. 36. Meikle, G. J.: Case of Hereditary Telangiectasia , Lancet 2:863-864 ( (Oct. 14) ) 1933. 37. Gerlings, P. G., and Polak, A.: Tracheobronchial Form of Hemorrhagic Angiomatosis of Osler: Two Cases , Bronchoscop., œsophagoscop. et gastroscop. , (July) 1938, pp. 175-180. 38. Cordier, V.; Lagèze, P., and Mounier-Kuhn, P. L.: Hemoptysis in Osler's Hemorrhagic Angiomatosis , Lyon méd. 156:51-54 ( (July 14) ) 1935. 39. Scheer, M.: A Case for Diagnosis (Hereditary Familial Telangiectasia) , Arch. Dermat. & Syph. 41:1189 ( (June) ) 1940. 40. Blum, V.: Familial Essential Hematuria and Its Association with Osler's Disease , Med. Klin. 32:1254-1255 ( (Sept. 11) ) 1936. 41. Keller, W.: Hematuria in Childhood: A Case of Probable Telangiectasia Hemorrhagica Hereditaria , Monatschr. f. Kinderh. 79:376-381, 1939. 42. Weber, F. P.: Hemorrhagic Hereditary Telangiectasia of Osler Type, with Multiple Pulsating Stellate Telangiectases , Brit. J. Dermat. 48:182 ( (April) ) 1936.Crossref 43. Pillsbury, D. M.: Multiple Hereditary Telangiectasia (Rendu-Weber-Osler Syndrome) , Arch. Dermat. & Syph. 32:145-146 ( (July) ) 1935. 44. Yde, A., and Olesen, M.: Hereditary Angiomatosis (Osler's Disease) in Two Danish Families , Hospitalstid. 77:1010-1023 ( (Sept. 18) ) 1934. 45. Bloom, D.: Osler's Disease (Hereditary Familial Telangiectasia) , Arch. Dermat. & Syph. 37:678-679 ( (April) ) 1938. 46. Combes, F. C.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 39:754 ( (April) ) 1939. 47. Hottenroth, H.: Contribution to Osler's Disease , Arch. f. Dermat. u. Syph. 178:582-592, 1939. 48. Halloran, C.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 45:175 ( (Jan.) ) 1942. 49. Raaschou, F.: Hereditary Hemorrhagic Telangiectasia (Rendu-Osler) with a Genealogic Table , abstracted, J. A. M. A. 118:258 ( (Jan. 17) ) 1942. 50. Theorin, S.: Eine Familie aus Norrland mit Morbus Rendu-Osler , Acta med. Scandinav. , 1941, (supp. 123) , p. 268. 51. Földváry, F.: Hereditary Hemorrhagic Telangiectasia , Magyar orvosi arch. 34:230-237, 1933. 52. Guy, W. H., and Amshel, F.: Familial Telangiectasia , Arch. Dermat. & Syph. 29:778 ( (May) ) 1934. 53. Madden, J. F.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 36:675 ( (Sept.) ) 1937. 54. Rulison, R. H.: Multiple Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 34:522-523 ( (Sept.) ) 1936. 55. Kindler, W.: Epistaxis in Angiomatosis (Osler's Disease) , Arch. f. Ohren-, Nasen- u. Kehlkopfh. 143:236-240, 1937. 56. Lynch, F. W.: Elastic Tissue in Fetal Skin , Arch. Dermat. & Syph. 29:57-79 ( (Jan.) ) 1934. 57. Pardo-Castello, V., and Farinas, E. P.: Hereditary Multiple Telangiectasia , Arch. Dermat. & Syph. 39:1025-1034 ( (June) ) 1939. 58. Neumark: La maladie d'Osler , in Deliberationes Congressus Dermatologorum Internationalis , Leipzig, Johann Ambrosius Barth, 1936, vol. 2, p. 746. 59. Ullmann, K.: Angiomatosis (Morbus Osler); Ist sie eine Blut- oder Gefasserkrankung? in Deliberationes Congressus Dermatologorum Internationalis , Leipzig, Johann Ambrosius Barth, 1936, vol. 2, p. 743. 60. Ormsby, O. S., and Montgomery, H.: Diseases of the Skin , ed. 6, Philadelphia, Lea & Febiger, 1943. 61. Footnote deleted by the author. 62. Lewis, P. M.: Angiomatosis Retinae , Memphis M. J. 18:146-150 ( (Oct.) ) 1943. 63. Bommer, S.: Microscopic Study of Capillaries in Hereditary Progressive Telangiectasis , Dermat. Wchnschr. 98:201-210 ( (Feb. 17) ) 1934. 64. O'Kane, G. H.: Hereditary Multiple Telangiectases with Epistaxis , J. A. M. A. 111:242-244 ( (July 16) ) 1938. 65. Biegeleisen, H. I.: Telangiectases of the Nose: Treatment by Micro-Injection of a Sclerosing Fluid , Ann. Otol., Rhin. & Laryng. 45:416-419 ( (June) ) 1936. 66. Watson, W. L., and McCarthy, W. D.: Blood and Lymph-Vessel Tumors: One Thousand and Fifty-Six Cases , Surg., Gynec. & Obst. 71:569-588 ( (Nov.) ) 1940. 67. Sterman, M. M., and Scal, J. C.: Familial Telangiectasia with Recurring Epistaxis Successfully Treated with Radium , New York State J. Med. 37:287-292 ( (Feb. 1) ) 1937. 68. Peck, S. M., and Rosenthal, N.: Effect of Moccasin Snake Venom (Ancistrodon Piscivorus) in Hemorrhagic Conditions , J. A. M. A. 104:1066-1070 ( (March 30) ) 1935.Crossref 69. Peck, S. M.: Osler's Hereditary Familial Telangiectases , Arch. Dermat. & Syph. 34:1060 ( (Dec.) ) 1936. 70. Ingels, A. E.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 41:986-987 ( (May) ) 1940. 71. Weiss, J. A.: Radium Therapy for Recurrent Epistaxis in Hereditary Hemorrhagic Telangiectasia , Laryngoscope 48:865-869 ( (Dec.) ) 1938. 72. Cipollaro, A. C.: Electrolysis , J. A. M. A. 111:2488-2491 ( (Dec. 31) ) 1938. 73. Weaver, D. F.: Three Unusual Cases of Hemangioma , Ann. Otol., Rhin. & Laryng. 52:507-515 ( (June) ) 1943. 74. Newcomet, W. S.: Treatment of Hemangioma , Am. J. Roentgenol. 39:470 ( (March) ) 1937. 75. Molesworth, E. H.: Importance of Early Treatment of Vascular Naevi , M. J. Australia 2:217 ( (Aug. 12) ) 1933. 76. Hare, H. F.: Problems of Radiation Therapy , Lahey Clin. Bull. 3:167-173 ( (Oct.) ) 1943. 77. Quick, A. J.: The Hemorrhagic Diseases and the Physiology of Hemostasis , Springfield, Ill., Charles C Thomas, Publisher, 1942. 78. Templeton, H. J.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 38:498-499 ( (Sept.) ) 1938. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Otolaryngology American Medical Association

HEREDITARY HEMORRHAGIC TELANGIECTASIA (OSLER'S DISEASE): A REVIEW OF THE LITERATURE AND REPORT OF CASES

Archives of Otolaryngology , Volume 40 (2) – Aug 1, 1944

Loading next page...
 
/lp/american-medical-association/hereditary-hemorrhagic-telangiectasia-osler-s-disease-a-review-of-the-9yD5uSyWZC
Publisher
American Medical Association
Copyright
Copyright © 1944 American Medical Association. All Rights Reserved.
ISSN
0003-9977
DOI
10.1001/archotol.1944.00680020140004
Publisher site
See Article on Publisher Site

Abstract

Abstract Hereditary hemorrhagic telangiectasia is a rare disease, probably due to mesenchymal dysplasia. It is characterized by the presence of multiple acquired angiomas or telangiectases of varying distribution and number with a marked tendency to bleed spontaneously or from slight trauma. The disease is not sex bound. It is transmitted as a dominant characteristic. The initial symptom usually consists of abnormally profuse epistaxis beginning about puberty. This is followed by the development of multiple telangiectasia of the skin and mucous membranes from the age of 25 to 35. Hemorrhage from the nasal mucosa is most frequent, and all symptoms tend to reach their greatest severity during the fourth decade. The average mortality rate is 4 per cent. The lesions are most commonly found in the nasal mucosa, the skin of the face, the buccal mucosa, the lips, the tongue, the floor of the mouth, the scalp, the ears, the conjunctivas and References 1. Houser, K. M.: Hereditary Hemorrhagic Telangiectasia , Ann. Otol., Rhin. & Laryng. 43:731-738 ( (Sept.) ) 1934. 2. Aubertin, C.; Levy, R., and Baclesse: L'angiomatose hemorragique familiale (maladie de Rendu-Osler) , Presse méd. 41:185-188 ( (Feb.) ) 1933. 3. Teahan, W. W.: Hereditary Hemorrhagic Telangiectasia Occurring in Six Generations , Ann. Int. Med. 13:535-543 ( (Sept.) ) 1939. 4. Alban, H.: Hereditary Hemorrhagic Telangiectasia , Northwest Med. 40:86-88 ( (March) ) 1941. 5. Goldstein, H. I.: Goldstein's Heredofamilial Angiomatosis with Recurring Familial Hemorrhage (Rendu-Osler-Weber's Disease) , Arch. Int. Med. 58:836-865 ( (Nov.) ) 1931. 6. Fingerland, A., and Janousek, B.: Hereditary Hemorrhagic Telangiectasia (Osler's Disease) , Arch. f. Dermat. u. Syph. 178:54-64, 1938. 7. Figi, F. A., and Watkins, C. H.: Hereditary Hemorrhagic Telangiectasia , Ann. Otol., Rhin. & Laryng. 52:330-341 ( (June) ) 1943. 8. Goldstein, H. I.: Hereditary Multiple Telangiectasia , Arch. Dermat. & Syph. 26:282-308 ( (Aug.) ) 1932. 9. Ullmann, K.: Angiomatosis (K. Ullmann) and Osler's Disease , Urol. & Cutan. Rev. 37:619-629 ( (Sept.) ) 1933. 10. Kufs, H.: Heredofamilial Angiomatosis of the Brain and Retina and Its Relationship to Skin Angiomatosis , Ztschr. f. d. ges. Neurol. u. Psychiat. 113:651-686, 1928. 11. Junius, P.: Relationship Between Angiomatosis of the Retina, Exudative Retinitis (Coat's) and Osler's Disease , Ztschr. f. Augenh. 84:193-210 ( (Oct.) ) 1934. 12. Michael, J. C., and Levin, P. M.: Multiple Telangiectases of the Brain: A Discussion of Hereditary Factors in Their Development , Arch. Neurol. & Psychiat. 36:514-529 ( (Sept.) ) 1936. 13. Ironside, R., and Hill, D.: Cutaneous Naevus with Buphthalmos and Epilepsy , J. Ment. Sc. 87:631-634 ( (Oct.) ) 1941. 14. Louis-Bar: Progressive Syndrome Consisting of Symmetric Cutaneous and Conjunctival Telangiectases and Cerebellar Manifestations , abstracted, Arch. Dermat. & Syph. 46:890 ( (Dec.) ) 1942. 15. Cordes, F. C., and Hogan, M. J.: Angiomatosis Retinae (Hippel's Disease) , Arch. Ophth. 23:253-269 ( (Feb.) ) 1940. 16. Madden, J. F.: Generalized Angiomatosis (Telangiectasia) , J. A. M. A. 102:442-448 ( (Feb. 10) ) 1934. 17. Muende, I.: Multiple Symmetrical Fibro-Angiomatous Nevi of the Face and Hands , Proc. Roy. Soc. Med. 27:292 ( (Jan.) ) 1934. 18. Goldstein, H. I.: Heredofamilial Angiomatosis (Telangiectasia) with Recurring Hemorrhages , Internat. Clin. 2:43-56 ( (June) ) 1934. 19. Kosiner, R.: Hereditary Hemorrhagic Telangiectasia , Klin. Wchnschr. 14:713-714 ( (May 18) ) 1935. 20. Netherton, E. W., and Curtis, G. H.: Raynaud's Disease with Subcutaneous Calcium Deposition in the Fingers and Hereditary Multiple Telangiectases , Arch. Dermat. & Syph. 46:579-580 ( (Oct.) ) 1942. 21. Kugelmass, I. N.: Hereditary Hemorrhagic Telangiectasis , J. A. M. A. 102:287-291 ( (Jan. 27) ) 1934.Crossref 22. Milbradt, W.: Atypical Diffuse Scleroderma with Osler Syndrome and Hepatic Dysfunction , Dermat. Wchnschr. 99:973-979 ( (July 28) ) 1934. 23. Harding, G.: Ein Fall von Morbus Osler , Acta med. Scandinav. 106:352-368, 1941.Crossref 24. van Bogaert, L.: Two Cases of Hereditary Hemorrhagic Angiomatosis with Hepatosplenomegaly and Two Cases of Hemorrhagic Telangiectasis in Same Family , Bull. et mém. Soc. méd. d. hôp. de Paris 49:1572-1578 ( (Dec. 25) ) 1933. 25. Davis, E.: Hereditary Familial Purpura Simplex , Lancet 2:1110-1114 ( (Nov. 25) ) 1939.Crossref 26. Bankoff, G.: Pathology and Therapy of Essential Telangiectases , München. med. Wchnschr. 80:2035-2037 ( (Dec. 29) ) 1933. 27. Combes, F. C.: Multiple Hereditary Telangiectasia (Osler's Disease) and Cardiovascular Syphilis , Arch. Dermat. & Syph. 44:114-115 ( (July) ) 1941. 28. Michelson, H. E.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 36:241 ( (July) ) 1937. 29. Obermayer, M. E., and Becker, S. W.: Generalized Telangiectasis , Arch. Dermat. & Syph. 43:1077 ( (June) ) 1941. 30. Becker, S. W., and Obermayer, M. E.: Telangiectasia Hemorrhagica Hereditaria (Osler's Disease) and Vitiligo , Arch. Dermat. & Syph. 44:303-304 ( (Aug.) ) 1941. 31. Zeisler, E. P.: Telangiectasia Associated with Syphilis and Pregnancy , Arch. Dermat. & Syph. 5:781 ( (June) ) 1922. 32. McDonough, F. E.; Dry, T. J., and Roth, G. M.: Hereditary Telangiectasia with Visceral Involvement: Special Studies of Skin Temperature; Report of a Case , Proc. Staff Meet., Mayo Clin. 15:593-604 ( (Sept. 18) ) 1940. 33. Renshaw, J. F.: Multiple Hemorrhagic Telangiectasia with Special Reference to Gastroscopic Appearance , Cleveland Clin. Quart. 6:226-230 ( (July) ) 1939. 34. Griggs, D. E., and Baker, M. Q.: Hereditary Hemorrhagic Telangiectasia with Gastro-Intestinal Bleeding , Am. J. Digest. Dis. 8:344-346 ( (Sept.) ) 1941. 35. Stellar, L. I.: Hereditary Telangiectasia: Report of a Case , New England J. Med. 226:336-338 ( (Feb. 26) ) 1942. 36. Meikle, G. J.: Case of Hereditary Telangiectasia , Lancet 2:863-864 ( (Oct. 14) ) 1933. 37. Gerlings, P. G., and Polak, A.: Tracheobronchial Form of Hemorrhagic Angiomatosis of Osler: Two Cases , Bronchoscop., œsophagoscop. et gastroscop. , (July) 1938, pp. 175-180. 38. Cordier, V.; Lagèze, P., and Mounier-Kuhn, P. L.: Hemoptysis in Osler's Hemorrhagic Angiomatosis , Lyon méd. 156:51-54 ( (July 14) ) 1935. 39. Scheer, M.: A Case for Diagnosis (Hereditary Familial Telangiectasia) , Arch. Dermat. & Syph. 41:1189 ( (June) ) 1940. 40. Blum, V.: Familial Essential Hematuria and Its Association with Osler's Disease , Med. Klin. 32:1254-1255 ( (Sept. 11) ) 1936. 41. Keller, W.: Hematuria in Childhood: A Case of Probable Telangiectasia Hemorrhagica Hereditaria , Monatschr. f. Kinderh. 79:376-381, 1939. 42. Weber, F. P.: Hemorrhagic Hereditary Telangiectasia of Osler Type, with Multiple Pulsating Stellate Telangiectases , Brit. J. Dermat. 48:182 ( (April) ) 1936.Crossref 43. Pillsbury, D. M.: Multiple Hereditary Telangiectasia (Rendu-Weber-Osler Syndrome) , Arch. Dermat. & Syph. 32:145-146 ( (July) ) 1935. 44. Yde, A., and Olesen, M.: Hereditary Angiomatosis (Osler's Disease) in Two Danish Families , Hospitalstid. 77:1010-1023 ( (Sept. 18) ) 1934. 45. Bloom, D.: Osler's Disease (Hereditary Familial Telangiectasia) , Arch. Dermat. & Syph. 37:678-679 ( (April) ) 1938. 46. Combes, F. C.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 39:754 ( (April) ) 1939. 47. Hottenroth, H.: Contribution to Osler's Disease , Arch. f. Dermat. u. Syph. 178:582-592, 1939. 48. Halloran, C.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 45:175 ( (Jan.) ) 1942. 49. Raaschou, F.: Hereditary Hemorrhagic Telangiectasia (Rendu-Osler) with a Genealogic Table , abstracted, J. A. M. A. 118:258 ( (Jan. 17) ) 1942. 50. Theorin, S.: Eine Familie aus Norrland mit Morbus Rendu-Osler , Acta med. Scandinav. , 1941, (supp. 123) , p. 268. 51. Földváry, F.: Hereditary Hemorrhagic Telangiectasia , Magyar orvosi arch. 34:230-237, 1933. 52. Guy, W. H., and Amshel, F.: Familial Telangiectasia , Arch. Dermat. & Syph. 29:778 ( (May) ) 1934. 53. Madden, J. F.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 36:675 ( (Sept.) ) 1937. 54. Rulison, R. H.: Multiple Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 34:522-523 ( (Sept.) ) 1936. 55. Kindler, W.: Epistaxis in Angiomatosis (Osler's Disease) , Arch. f. Ohren-, Nasen- u. Kehlkopfh. 143:236-240, 1937. 56. Lynch, F. W.: Elastic Tissue in Fetal Skin , Arch. Dermat. & Syph. 29:57-79 ( (Jan.) ) 1934. 57. Pardo-Castello, V., and Farinas, E. P.: Hereditary Multiple Telangiectasia , Arch. Dermat. & Syph. 39:1025-1034 ( (June) ) 1939. 58. Neumark: La maladie d'Osler , in Deliberationes Congressus Dermatologorum Internationalis , Leipzig, Johann Ambrosius Barth, 1936, vol. 2, p. 746. 59. Ullmann, K.: Angiomatosis (Morbus Osler); Ist sie eine Blut- oder Gefasserkrankung? in Deliberationes Congressus Dermatologorum Internationalis , Leipzig, Johann Ambrosius Barth, 1936, vol. 2, p. 743. 60. Ormsby, O. S., and Montgomery, H.: Diseases of the Skin , ed. 6, Philadelphia, Lea & Febiger, 1943. 61. Footnote deleted by the author. 62. Lewis, P. M.: Angiomatosis Retinae , Memphis M. J. 18:146-150 ( (Oct.) ) 1943. 63. Bommer, S.: Microscopic Study of Capillaries in Hereditary Progressive Telangiectasis , Dermat. Wchnschr. 98:201-210 ( (Feb. 17) ) 1934. 64. O'Kane, G. H.: Hereditary Multiple Telangiectases with Epistaxis , J. A. M. A. 111:242-244 ( (July 16) ) 1938. 65. Biegeleisen, H. I.: Telangiectases of the Nose: Treatment by Micro-Injection of a Sclerosing Fluid , Ann. Otol., Rhin. & Laryng. 45:416-419 ( (June) ) 1936. 66. Watson, W. L., and McCarthy, W. D.: Blood and Lymph-Vessel Tumors: One Thousand and Fifty-Six Cases , Surg., Gynec. & Obst. 71:569-588 ( (Nov.) ) 1940. 67. Sterman, M. M., and Scal, J. C.: Familial Telangiectasia with Recurring Epistaxis Successfully Treated with Radium , New York State J. Med. 37:287-292 ( (Feb. 1) ) 1937. 68. Peck, S. M., and Rosenthal, N.: Effect of Moccasin Snake Venom (Ancistrodon Piscivorus) in Hemorrhagic Conditions , J. A. M. A. 104:1066-1070 ( (March 30) ) 1935.Crossref 69. Peck, S. M.: Osler's Hereditary Familial Telangiectases , Arch. Dermat. & Syph. 34:1060 ( (Dec.) ) 1936. 70. Ingels, A. E.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 41:986-987 ( (May) ) 1940. 71. Weiss, J. A.: Radium Therapy for Recurrent Epistaxis in Hereditary Hemorrhagic Telangiectasia , Laryngoscope 48:865-869 ( (Dec.) ) 1938. 72. Cipollaro, A. C.: Electrolysis , J. A. M. A. 111:2488-2491 ( (Dec. 31) ) 1938. 73. Weaver, D. F.: Three Unusual Cases of Hemangioma , Ann. Otol., Rhin. & Laryng. 52:507-515 ( (June) ) 1943. 74. Newcomet, W. S.: Treatment of Hemangioma , Am. J. Roentgenol. 39:470 ( (March) ) 1937. 75. Molesworth, E. H.: Importance of Early Treatment of Vascular Naevi , M. J. Australia 2:217 ( (Aug. 12) ) 1933. 76. Hare, H. F.: Problems of Radiation Therapy , Lahey Clin. Bull. 3:167-173 ( (Oct.) ) 1943. 77. Quick, A. J.: The Hemorrhagic Diseases and the Physiology of Hemostasis , Springfield, Ill., Charles C Thomas, Publisher, 1942. 78. Templeton, H. J.: Hereditary Hemorrhagic Telangiectasia , Arch. Dermat. & Syph. 38:498-499 ( (Sept.) ) 1938.

Journal

Archives of OtolaryngologyAmerican Medical Association

Published: Aug 1, 1944

References