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  Vol. 28 No. 4, October 1942 TABLE OF CONTENTS
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FOSTER KENNEDY SYNDROME ASSOCIATED WITH NON-NEOPLASTIC INTRACRANIAL CONDITIONS

H. EDWARD YASKIN, M.D.; N. S. SCHLEZINGER, M.D.

Arch Ophthal. 1942;28(4):704-710.

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

Leslie Paton1 in 1909 was the first to call attention to the observation that in association with a basofrontal tumor there is apt to be atrophy of the optic nerve on the side of the tumor and choked disk on the opposite side. However, it was Foster Kennedy,2 in 1911, who emphasized and amplified this ophthalmologic symptom complex, which he felt was diagnostic of the presence of a basofrontal tumor or abscess. According to him the symptom complex comprised the existence of a central scotoma and primary optic nerve atrophy in the eye on the side of the lesion with concomitant papilledema in the opposite eye. Since that time this syndrome has been included in practically all the standard textbooks on neurology and has come to be recognized, when present, as a diagnostic criterion of the existence of an expanding lesion of the basofrontal region or the anterior . . . [Full Text PDF of this Article]


Author Affiliations

PHILADELPHIA

From the Department of Neurology, Jefferson Medical College of Philadelphia.



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