This Article  • References  • Full text PDF  • Send to a friend  • Save in My Folder  • Save to citation manager  • Permissions  Citing Articles  • Citation map  • Citing articles on HighWire  • Citing articles on Web of Science (21)  • Contact me when this article is cited  Related Content  • Similar articles in this journal  Social Bookmarking   What's this?

Report of a Case with Coincidental Osteitis Deformans and Review of the Literature

LESLIE J. LEVENE, M.B., B.S.

AMA Arch Intern Med. 1959;103(4):570-580.

	Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

Introduction

Even before von Recklinghausen's original monograph, in 1882,¹ the literature has contained references to various bone changes complicating neurofibromatosis, e. g., bowing and pseudarthroses,² disorders of growth.³ Indeed, Wilson⁴ includes bone affection in his definition of the syndrome, and Saville et al.⁵ state that neurofibromatosis is characterized by lesions of skin, nerve, and bone.

Diverse secondary features other than bony which are said to occur can be grouped into psychological and endocrine. Regarding the former, perhaps the most pertinent comment is made by Wilson,⁴ "that some sufferers from a disease marked by unsightly deformities and disfigurements, especially when the face is concerned, should become sensitive, despondent or misanthropic need occasion no surprise." Authors further reflect that of diverse psychical disorders reported in connection with the malady none is specific and most are purely incidental.

Various investigators, including Preiser and Davenport ⁶ and Yakovlev and Guthrie,⁷ have reported an increased . . . [Full Text PDF of this Article]

Author Affiliations
Sunderland, England

Formerly Registrar, Geriatric Unit, Sunderland General Hospital.

Footnotes
Submitted for publication June 2, 1958.

CiteULike    Connotea    Del.icio.us    Digg    Reddit    Technorati    Twitter     What's this?