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  Vol. 234 No. 11, December 15, 1975 TABLE OF CONTENTS
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Mumps Meningoencephalitis

Prolonged Abnormality of Cerebrospinal Fluid

Parvin H. Azimi, MD; Sedat Shaban, MD; Milo D. Hilty, MD; Ralph E. Haynes, MD

JAMA. 1975;234(11):1161-1162.

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

MUMPS meningoencephalitis is usually a benign self-limiting disease; its clinical features are fever, headache, nausea, vomiting, and meningeal signs. The clinical course is of short duration, and death or major neurological complications are rare.

The patient with mumps meningoencephalitis described in this report is unusual because of the persistence of an elevated cerebrospinal fluid (CSF) protein level and pleocytosis.

Report of a Case

An 11-year-old boy was admitted to Columbus (Ohio) Children's Hospital on Aug 6, 1973. Five days prior to admission, earache, fever, vomiting, and ataxia had developed. The following day, his temperature rose to 40 C (104 F). His physician gave him an injection of penicillin, and ampicillin in a dosage of 500 mg orally every six hours was prescribed. In spite of antibiotic therapy, his illness progressed and he was admitted to the hospital because of confusion and visual hallucinations. At the time of admission, his temperature . . . [Full Text PDF of this Article]


Author Affiliations

From the departments of pediatrics and medical microbiology, Ohio State University College of Medicine (Drs Azimi and Haynes), and the Department of Pediatrics (Drs Shaban and Hilty) and the Infectious Disease Division (Drs Haynes and Azimi), Children's Hospital, Columbus.


Footnotes

Reprint requests to Department of Medical Microbiology, Ohio State University College of Medicine, 333 W Tenth Ave, Columbus, OH 43210 (Dr Azimi).



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