Positive Culture from Normal CSF of <i>Streptococcus pneumoniae </i>Meningitis
Author(s) -
Toshiki Uchihara,
Kenji Ichikawa,
Shōji Yoshida,
Hiroshi Tsukagoshi
Publication year - 1996
Publication title -
european neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.573
H-Index - 77
eISSN - 1421-9913
pISSN - 0014-3022
DOI - 10.1159/000117256
Subject(s) - streptococcus pneumoniae , meningitis , medicine , cerebrospinal fluid , microbiology and biotechnology , immunology , pathology , biology , antibiotics , pediatrics
We successfully treated a non-immunocompromised patient with meningitis due to Streptococcus pneumoniae whose initial lumbar puncture was normal. A 52-year-old male farmer was admitted because of general malaise and shaking chill (body temperature 39.3 ° C) with headache and nausea. He had been in good health and the family history was negative. The bilateral tenderness in the costovertebral angle was noted. He was fully conscious. No signs of meningeal irritation nor focal neurological deficits were noted. Urinalysis revealed numerous white blood cells and bacteria (Proteus vulgaris). A lumbar puncture yielded a clear colorless cerebrospinal fluid (CSF) containing no red blood cells, six white cells/mm (poly-mophonucleanmononuclear = 2:4), 26 mg/dl of protein and 71 mg/dl of glucose. The circulating blood count showed leukocytosis (27,800/ mm) with a shift to the left. Intravenous cefmenoxime (2 g/day) was initiated for suspected pyelonephritis. He became gradually disoriented, accompanied by dilated pupils and Kernig’s sign. The brain CT was normal. The second CSF obtained 12 h after the initial one contained 2,709 white cells/mm (polymorphonuclear:mononuclear = 98:2), 360 mg/dl of protein, 13 mg/dl of glucose and numerous gram-positive diplococci. The CSF reacted with the latex coated with the antipneumococcal polysaccharide antibody. In spite of 24 million units/day of intravenous penicillin-G, the patient’s consciousness declined further to deep coma. Streptococcus pneumoniae was cultured from the CSF obtained at the initial and the second lumbar puncture and from the initial blood cultures. Penicillin-G was switched to ampicillin 18 g/day plus refampin 450 mg/day according to the sensitivity test. He regained consciousness and was discharged without deficit. Bacterial meningitis with no or slight changes in the CSF has rarely been reported [1,2]. Gorse et al. [3] reported cases of Clostridium meningitis without pleocytosis. Fishbein et al. [4] reported 7 cases of bacterial meningitis without remarkable changes in CSF. All of their cases [4] had an underlying disease such as Hodgkin’s disease or alcoholism etc. and, therefore, the inflammatory reactions such as fever or leucocytosis were relatively mild as well as in the CSF. A lumbar puncture may potentially induce meningitis especially in patients with septicemia [2, 3, 5–7]. Experimentally, Petersdorf and Luttrell [8] induced a cisternal puncture on dogs with pneumococcemia. On clinical grounds, however, Pray [9] found no difference in the appearance rate of meningitis between septic patients who underwent a lumbar puncture and those who did not. In our patient, the ‘normal’ CSF obtained at the initial lumbar puncture contained Streptococcus pneumoniae which was already present in the lumbar region, not introduced by the initial lumbar puncture. On the other hand, the patient complained of headache beforehand, which suggests that a meningeal irritation was already present in the cranium. Seemingly, it takes some time for the inflammatory reaction to spread from the intracranial cavity to the lumbar subarachnoid space. Okabe et al. [10] reported a similar case and estimated that the delay is 9–15 h. Although nonspecific, clinical symptoms such as headache and nausea associated with high fever were the only clues at the onset to suggest meningitis in our patient. Common pathogen such as Streptococcus pneumoniae may potentially cause meningitis without remarkable changes in the CSF at the onset even in a patient without notable underlying disorders.
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