Meningitis
Meningitis is the inflammation of the protective membranes covering the central nervous system, known collectively as the meninges. Meningitis
may develop in response to a number of causes, most prominently bacteria, viruses and other infectious agents, but also physical injury, cancer, or
certain drugs. While some forms of meningitis are mild and resolve on their own, meningitis is a potentially serious condition owing to the proximity
of the inflammation to the brain and spinal cord. The potential for serious neurological damage or even death necessitates prompt medical attention
and evaluation. Infectious meningitis, the most common form, is typically treated with antibiotics and requires close observation. Some forms of
meningitis (such as those associated with meningococcus, mumps virus or pneumococcus infections) may be prevented with immunization.
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Signs and Symptoms
Headache is the most common symptom of meningitis (87 percent) followed by nuchal rigidity ("neck stiffness", 83 percent). The classic triad of
diagnostic signs consists of nuchal rigidity (being unable to flex the neck forward), fever and altered mental status. All three features are present
in only 44% of all cases of infectious meningitis. Other signs commonly associated with meningitis are photophobia (inability to tolerate bright
light), phonophobia (inability to tolerate loud noises), irritability and delirium (in small children) and seizures (in 20-40% of cases). In infants
(0-6 months), swelling of the fontanelle (soft spot) may be present.
Nuchal rigidity is typically assessed with the patient lying supine, and both hips and knees flexed. If pain is elicited when the knees are passively
extended (Kernig's sign), this indicates nuchal rigidity and meningitis. In infants, forward flexion of the neck may cause involuntary knee and hip
flexion (Brudzinski's sign). Although commonly tested, the sensitivity and specificity of Kernig's and Brudzinski's tests are uncertain.
In "meningococcal" meningitis (i.e. meningitis caused by the bacteria Neisseria meningitidis), a rapidly-spreading petechial rash is typical, and may
precede other symptoms. The rash consists of numerous small, irregular purple or red spots on the trunk, lower extremities, mucous membranes, conjunctiva,
and occasionally on the palms of hands and soles of feet. Other clues to the nature of the cause may be the skin signs of hand, foot and mouth disease
and genital herpes, both of which may be associated with viral meningitis.
Diagnosis
Investigations
The suspicion of meningitis is generally based on the nature of the symptoms and findings on physical examination. Meningitis is a medical emergency,
and referral to hospital is indicated. If meningitis is suspected based on clinical examination, early administration of antibiotics is recommended,
as the condition may deteriorate rapidly. In the hospital setting, initial management consists of stabilization (e.g. securing the airway in a depressed
level of consciousness, administration of intravenous fluids in hypotension or shock), followed by antibiotics if not already administered.
Investigations include blood tests (electrolytes, liver and kidney function, inflammatory markers and a complete blood count) and usually X-ray
examination of the chest. The most important test in identifying or ruling out meningitis is analysis of the cerebrospinal fluid (fluid that envelops
the brain and the spinal cord) through lumbar puncture (LP). However, if the patient is at risk for a cerebral mass lesion or elevated intracranial
pressure (recent head injury, a known immune system problem, localizing neurological signs, or evidence on examination of a raised ICP), a lumbar
puncture may be contraindicated because of the possibility of fatal brain herniation. In such cases a CT or MRI scan is generally performed prior to
the lumbar puncture to exclude this possibility. Otherwise, the CT or MRI should be performed after the LP, with MRI preferred over CT due to its
superiority in demonstrating areas of cerebral edema, ischemia, and meningeal inflammation.
During the lumbar puncture procedure, the opening pressure is measured. A pressure of over 180 mm H2O is indicative of bacterial meningitis.
The cerebrospinal fluid (CSF) sample is examined for white blood cells (and which subtypes), red blood cells, protein content and glucose level. Gram
staining of the sample may demonstrate bacteria in bacterial meningitis, but absence of bacteria does not exclude bacterial meningitis; microbiological
culture of the sample may still yield a causative organism. The type of white blood cell predominantly present predicts whether meningitis is due to
bacterial or viral infection. Other tests performed on the CSF sample include latex agglutination test, limulus lysates, or polymerase chain reaction
(PCR) for bacterial or viral DNA. If the patient is immunocompromised, testing the CSF for toxoplasmosis, Epstein-Barr virus, cytomegalovirus, JC
virus and fungal infection may be performed.
CSF Finding in Different Conditions
| Condition | Glucose | Protein | Cells |
| Acute Bacterial Meningitis | Low | High | High, often > 300/mm3 |
| Acute Viral Meningitis | Normal | Normal or High | Mononuclear, < 300mm3 |
| Tuberculous Meningitis | Low | High | Pleocytosis, mixed < 300mm3 |
| Fungal Meningitis | Low | High | < 300mm3 |
| Malignant Meningitis | Low | High | Usually Mononuclear |
| Subarachnoid Hemmorhage | Normal | Normal or High | Erythrocytes |
In bacterial meningitis, the CSF glucose to serum glucose ratio is < 0.4. The Gram stain is positive in >60% of cases, and culture in >80%.
Latex agglutination may be positive in meningitis due to Streptococcus pneumoniae, Neisseria meningitidis, Haemophilus influenzae, Escherichia coli,
Group B Streptococci. Limulus lysates may be positive in Gram-negative meningitis.
Cultures are often negative if CSF is taken after the administration of antibiotics. In these patients, PCR can be helpful in arriving at a diagnosis.
It has been suggested that CSF cortisol measurement may be helpful.
Aseptic meningitis refers to non-bacterial causes of meningitis and includes infective etiologies such as viruses and fungi, neoplastic etiologies such
as carcinomatous and lymphomatous meningitis, inflammatory causes such as sarcoidosis (neurosarcoidosis)) and chemical causes such as meningitis
secondary to the intrathecal introduction of contrast media.
Although the term "viral meningitis" is often used in any patient with a mild meningeal illness with appropriate CSF findings, certain patients will
present with clinical and CSF features of viral meningitis, yet ultimately be diagnosed with one of the other conditions categorized as "aseptic
meningitis". This may be prevented by performing polymerase chain reaction or serology on CSF or blood for common viral causes of meningitis
(enterovirus, herpes simplex virus 2 and mumps in those not vaccinated for this).
A related diagnostic and therapeutic conundrum is the "partially treated meningitis", i.e. meningitis symptoms in patients who have already been
receiving antibiotics (such as for presumptive sinusitis). In these patients, CSF findings may resemble those of viral meningitis, but antibiotic
treatment may need to be continued until there is definitive positive evidence of a viral cause (e.g. a positive enterovirus PCR).
Prediction Rules
The Bacterial Meningitis Score predicts reliably whether a child (older than two months) may have infectious meningitis. In children with at least 1
risk factor (positive CSF Gram stain, CSF absolute neutrophil count ≥ 1000 cell/µL, CSF protein ≥ 80 mg/dL, peripheral blood absolute neutrophil count
≥ 10,000 cell/µL, history of seizure before or at presentation time) it had a sensitivity of 100%, specificity of 63.5%, and negative predictive value
of 100%.
Causes
Most cases of meningitis are caused by microorganisms, such as viruses, bacteria, fungi, or parasites, that spread into the blood and into the
cerebrospinal fluid (CSF). Non-infectious causes include cancers, systemic lupus erythematosus and certain drugs. The most common cause of meningitis
is viral, and often runs its course within a few days. Bacterial meningitis is the second most frequent type and can be serious and life-threatening.
Numerous microorganisms may cause bacterial meningitis, but Neisseria meningitidis ("meningococcus") and Streptococcus pneumoniae ("pneumococcus")
are the most common pathogens in patients without immune deficiency, with meningococcal disease being more common in children. Staphylococcus aureus
may complicate neurosurgical operations, and Listeria monocytogenes is associated with poor nutritional state and alcoholicism. Haemophilus influenzae
(type B) incidence has been much reduced by immunization in many countries. Mycobacterium tuberculosis (the causative agent of tuberculosis) rarely
causes meningitis in Western countries but is common and feared in countries where tuberculosis is endemic.
Treatment
Bacterial Meningitis
Bacterial meningitis is a medical emergency and has a high mortality rate if untreated. All suspected cases, however mild, need emergency medical
attention. Empiric antibiotics must be started immediately, even before the results of the lumbar puncture and CSF analysis are known. Antibiotics
started within 4 hours of lumbar puncture will not significantly affect lab results. Adjuvant treatment with corticosteroids reduces rates of
mortality, severe hearing loss and neurological sequelae in adults, specifically when the causative agent is Pneumococcus.
| Age Group | Causes |
| Neonates | Group B Streptococci, Escherichia coli, Listeria monocytogenes |
| Infants | Neisseria meningitidis, Haemophilus influenzae, Streptococcus pneumoniae |
| Children | N. meningitidis, S. pneumoniae |
| Adults | S. pneumoniae, N. meningitidis, Mycobacteria, Cryptococci |
The choice of antibiotic depends on local advice. In most of the developed world, the most common organisms involved are Streptococcus pneumoniae and
Neisseria meningitidis: first line treatment in the UK is a third-generation cephalosporin (such as ceftriaxone or cefotaxime). In those under 3 years
of age, over 50 years of age, or immunocompromised, ampicillin should be added to cover Listeria monocytogenes. In the U.S. and other countries with
high levels of penicillin resistance, the first line choice of antibiotics is vancomycin and a carbapenem (such as meropenem). In sub-Saharan Africa,
oily chloramphenicol or ceftriaxone are often used because only a single dose is needed in most cases.
Staphylococci and gram-negative bacilli are common infective agents in patients who have just had a neurosurgical procedure. Again, the choice of
antibiotic depends on local patterns of infection: cefotaxime and ceftriaxone remain good choices in many situations, but ceftazidime is used when
Pseudomonas aeruginosa is a problem, and intraventricular vancomycin is used for those patients with intraventricular shunts because of high rates
of staphylococcal infection. In patients with intracerebral prosthetic material (metal plates, electrodes or implants, etc.) then sometimes
chloramphenicol is the only antibiotic that will adequately cover infection by Staphylococcus aureus (cephalosporins and carbapenems are inadequate
under these circumstances).
Once the results of the CSF analysis are known along with the Gram-stain and culture, empiric therapy may be switched to therapy targeted to the
specific causative organism and its sensitivities.
- Neisseria meningitidis (Meningococcus) can usually be treated with a 7-day course of IV antibiotics:
- Penicillin-sensitive -- penicillin G or ampicillin
- Penicillin-resistant -- ceftriaxone or cefotaxime
- Prophylaxis for close contacts (contact with oral secretions) -- rifampin 600 mg bid for 2 days (adults) or 10 mg/kg bid (children). Rifampin is not recommended in pregnancy and as such, these patients should be treated with single doses of ciprofloxacin, azithromycin, or ceftriaxone
- Streptococcus pneumoniae (Pneumococcus) can usually be treated with a 2-week course of IV antibiotics:
- Penicillin-sensitive -- penicillin G
- Penicillin-intermediate -- ceftriaxone or cefotaxime
- Penicillin-resistant -- ceftriaxone or cefotaxime + vancomycin
- Listeria monocytogenes is treated with a 3-week course of IV ampicillin + gentamicin.
- Gram negative bacilli -- ceftriaxone or cefotaxime
- Pseudomonas aeruginosa -- ceftazidime
- Staphylococcus aureus
- Methicillin-sensitive -- nafcillin
- Methicillin-resistant -- vancomycin
- Streptococcus agalactiae -- penicillin G or ampicillin
- Haemophilus influenzae -- ceftriaxone or cefotaxime
Viral Meningitis
Patients diagnosed with mild viral meningitis may improve quickly enough to not require admission to a hospital, whilst others may be hospitalised
for many more days for observation and supportive care. Overall, the illness is usually much less severe than bacterial meningitis.
Unlike bacteria, viruses cannot be killed by antibiotics although drugs such as acyclovir may be employed, especially if herpes virus infection is
either suspected or demonstrated.
Fungal Meningitis
This form of meningitis is rare in otherwise healthy people, but is a higher risk in those who have AIDS, other forms of immunodeficiency (an immune
system that does not respond adequately to infections) and immunosuppression (immune system malfunction as a result of medical treatment). In AIDS,
Cryptococcus neoformans is the most common cause of fungal meningitis; it requires Indian ink staining of the CSF sample for identification of this
capsulated yeast. Fungal meningitis is treated with long courses of highly dosed antifungals.
Complications
In children there are several potential disabilities which result from damage to the nervous system. These include sensorineural hearing loss, epilepsy,
diffuse brain swelling, hydrocephalus, cerebral vein thrombosis, intra cerebral bleeding and cerebral palsy. Acute neurological complications may
lead to adverse consequences. In childhood acute bacterial meningitis deafness is the most common serious complication. Sensorineural hearing loss
often develops during first few days of the illness as a result of inner ear dysfunction, but permanent deafness is rare and can be prevented by prompt
treatment of meningitis.
Those that contract the disease during the neonatal period and those infected by S. pneumoniae and gram negative bacilli are at greater risk of
developing neurological, auditory, or intellectual impairments or functionally important behaviour or learning disorders which can manifest as poor
school performance.
In adults central nervous system complications include brain infarction, brain swelling, hydrocephalus, intracerebral bleeding; systemic complications
are dominated by septic shock, adult respiratory distress syndrome and disseminated intravascular coagulation. Those who have underlying
predisposing conditions e.g. head injury may develop recurrent meningitis. Case-fatality ratio is highest for gram-negative etiology and lowest
for meningitis caused by H. influenzae (also a gram negative bacilli). Fatal outcome in patients over 60 years of age is more likely to be from systemic
complications e.g. pneumonia, sepsis, cardio-respiratory failure; however in younger individuals it is usually associated with neurological
complications. Age more than 60, low Glasgow coma scale at presentation and seizure within 24 hours increase the risk of death among community
acquired meningitis.
Prevention
Immunization
Vaccinations against Haemophilus influenzae (Hib) have decreased early childhood meningitis significantly.
Vaccines against type A and C Neisseria meningitidis, the kind that causes most disease in preschool children and teenagers in the United States, have
also been around for a while. Type A is also prevalent in sub-Sahara Africa and W135 outbreaks have affected those on the Hajj pilgrimage to Mecca.
Immunisation with the ACW135Y vaccine against four strains is now a visa requirement for taking part in the Hajj.
Vaccines against Type B Neisseria meningitidis are much harder to produce, as its capsule is very weakly immunogenic masking its antigenic proteins.
There is also a risk of autoimmune response, and the porA and porB proteins on Type B resemble neuronal molecules. A vaccine called MeNZB for a
specific strain of type B Neisseria meningitidis prevalent in New Zealand has completed trials and is being given to many people in the country under
the age of 20 free of charge. There is also a vaccine, MenBVac, for the specific strain of type B meningoccocal disease prevalent in Norway, and
another specific vaccine for the strain prevalent in Cuba.
Pneumococcal polysaccharide vaccine against Streptococcus pneumoniae is recommended for all people 65 years of age or older. Pneumococcal conjugate
vaccine is recommended for all newborns starting at 6 weeks - 2 months, according to American Association of Pediatrics (AAP) recommendations.
Mumps vaccination has led to a sharp decline in mumps virus associated meningitis, which prior to vaccination occurred in 15% of all cases of mumps.
Prophylaxis
In cases of meningococcal meningitis, prophylactic treatment of close relatives with antibiotics (e.g. rifampicin, ciprofloxacin or ceftriaxone) may
reduce the risk of further cases.
Epidemiology
Meningitis can affect anyone in any age group, from the newborn to the elderly.
The "Meningitis Belt" is an area in sub-Saharan Africa which stretches from Senegal in the west to Ethiopia in the east in which large epidemics of
meningococcal meningitis occur (this largely coincides with the Sahel region). It contains an estimated total population of 300 million people. The
largest epidemic outbreak was in 1996, when over 250,000 cases occurred and 25,000 people died as a consequence of the disease.
History
Meningitis was first described in the 1020s in Avicenna's The Canon of Medicine, and again more accurately by Avenzoar of al-Andalus in the 12th
century. Symptoms of the disease were also noted in 1805 by the Swiss Gabinetto Vieusseux (a scientific-literary association) during an outbreak
in Geneva, Switzerland. In 1887, Dr. Anton Weichselbaum (1845-1920) of Vienna became the first to isolate the specific germ, meningococcus.
In the 19th century, meningitis was a scourge of the Japanese imperial family, playing the largest role in the horrendous pre-maturity mortality rate
the family endured. In the mid-1800s, only the Emperor Kōmei and two of his siblings reached maturity out of fifteen total children surviving birth.
Kōmei's son, the Emperor Meiji, was one of two survivors out of Kōmei's six children, including an elder brother of Meiji who would have taken the
throne had he lived to maturity. Five of Meiji's 15 children survived, including only his third son, Emperor Taishō, who was feeble-minded, perhaps
as a result of having contracted meningitis himself. By Emperor Hirohito's generation the family was receiving modern medical attention. As the focal
point of tradition in Japan, during the Tokugawa Shogunate the family was denied modern "Dutch" medical treatment then in use among the upper caste;
despite extensive modernization during the Meiji Restoration the Emperor insisted on traditional medical care for his children.
(adapted from Wikipedia, the free encyclopedia http://en.wikipedia.org/wiki/Meningitis)
Authors: Chamberlain MC, Glantz M.
Department of Neurology, University of Washington, Fred Hutchinson Cancer Center, Seattle, Washington.
BACKGROUND: The most frequent nervous system complications of multiple myeloma are peripheral neuropathy and epidural spinal cord compression. Myelomatous meningitis (MM) has been considered rare. The current study was performed to characterize the clinical presentation, treatment, and outcome of MM. METHODS: The study was a case series of 14 patients with cerebrospinal fluid (CSF)-positive MM who were treated at a tertiary care university medical center. RESULTS: Fourteen patients with advanced multiple myeloma were treated with involved-field radiotherapy (to the brain in 5 patients and the spine in 6 patients) and intra-CSF chemotherapy (ventricular in 10 patients and lumbar in 4 patients). The best response to treatment included 6 partial responses and 8 patients with progressive disease. The median duration of response was 2.5 months (range, 0-6 months). Cause of death was progressive neurologic disease in 6 patients, combined systemic and neurologic disease in 6 patients, and systemic disease progression in 2 patients. CONCLUSIONS: MM is rare and morbid entity (6-month neurologic disease progression-free survival rate of 7%), and appears to be no more responsive to treatment than solid tumor carcinomatous meningitis. Cancer 2008. (c) 2008 American Cancer Society.
Journal: Cancer. 2008 Feb 7
Authors: Maconochie I, Baumer H, Stewart M.
BACKGROUND: Acute bacterial meningitis remains a disease with high mortality and morbidity rates. However, with prompt and adequate antimicrobial and supportive treatment, the chances for survival have improved, especially in infants and children. Careful management of fluid and electrolyte balance is an important supportive therapy. Both over- and under-hydration are associated with adverse outcomes. OBJECTIVES: To evaluate differing volumes of fluid given in the initial management of bacterial meningitis. SEARCH STRATEGY: We searched the Cochrane Acute Respiratory Infection Group's trials register, the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library 2007, Issue 1), MEDLINE (1966 to March 2007), EMBASE (1980 to March 2007), and CINAHL (1982 to February 2007). SELECTION CRITERIA: Randomised controlled trials of differing volumes of fluid given in the initial management of bacterial meningitis were eligible for inclusion. DATA COLLECTION AND ANALYSIS: Six trials were identified in the initial search. On careful inspection three of these met the inclusion criteria. Data were extracted and trials were assessed for quality by all four of the original review authors (one author, R.O.W. has died since the original review, see acknowledgements). Data were combined for meta-analysis using relative risks for dichotomous data or weighted mean difference for continuous data. A fixed-effect statistical model was used. MAIN RESULTS: The largest of the three trials was conducted in settings with high mortality rates. The meta-analysis found no significant difference between the maintenance-fluid and restricted-fluid groups in number of deaths (RR 0.82, 95% CI 0.53 to 1.27); acute severe neurological sequelae (RR 0.67, 95% CI 0.41 to 1.08); or in mild to moderate sequelae (RR 1.24, 95% CI 0.58 to 2.65). However, when neurological sequelae were defined further, there was a statistically significant difference in favour of the maintenance-fluid group in regard to spasticity (RR 0.50, 95% CI 0.27 to 0.93), seizures at both 72 hours (RR 0.59, 95% CI 0.42 to 0.83) and 14 days (RR 0.19, 95% CI 0.04 to 0.88), and chronic severe neurological sequelae at three-months follow up (RR 0.42, 95% CI 0.20 to 0.89). AUTHORS' CONCLUSIONS: Some evidence supports maintaining intravenous fluids rather than restricted them in the first 48 hours, in settings with high mortality rates and where patients present late. However, where children present early and mortality rates are lower there is insufficient evidence to guide practice.
Journal: Cochrane Database Syst Rev. 2008 Jan 23;(1):CD004786.
Authors: Hochberg NS, Park SY, Blackburn BG, Sejvar JJ, Gaynor K, Chung H, Leniek K, Herwaldt BL, Efflert PV.
Centers for Disease Control and Prevention, Atlanta, Georgia, USA. natasha_hochberg@post.harvard.edu
During November 2004-January 2005, 5 cases of eosinophilic meningitis (EM) attributable to Angiostrongylus cantonensis infection were reported in Hawaii. To determine if this temporal clustering reflected an increased incidence, we ascertained EM and A. cantonensis cases by systematic review of statewide laboratory and medical records for January 2001-February 2005 and generalized the data to population estimates. We identified 83 EM cases; 24 (29%) were attributed to A. cantonensis infection, which was included in the discharge diagnoses for only 2 cases. Comparison of A. cantonensis infection incidence rates (per 100,000 person-years) for the baseline (January 2001-October 2004) and cluster (November 2004-February 2005) periods showed statistically significant increases for the state as a whole (0.3 vs. 2.1), the Big Island of Hawaii (1.1 vs. 7.4), and Maui County (0.4 vs. 4.3). These findings underscore the need to consider the diagnosis of A. cantonensis infection, especially in the state of Hawaii.
Journal: Emerg Infect Dis. 2007 Nov;13(11):1675-80.
Authors: Mikdashi J, Kennedy S, Krumholz A.
From the *Departments of *Medicine and †Neurology, University of Maryland School of Medicine, Baltimore, MD.
BACKGROUND:: Aseptic meningitis is one of the most infrequent neuropsychiatric manifestations of systemic lupus erythematosus (SLE) with multifactorial etiologies including medications such as nonsteroidal anti-inflammatory drugs, azathioprine, and trimethoprim-sulfamethoxasole, as well as viruses and malignancy. Recurrent aseptic meningitis in SLE is rare, and remains a diagnostic challenge. METHODS:: We report a unique SLE patient with recurrent (10 episodes), benign (self-limited) lymphocytic aseptic meningitis, which suggests the diagnosis of Mollaret meningitis. There was no prior use of medications known to provoke meningitis. No infectious etiology was identified and chronic meningitis was not observed. The patient had spontaneous resolution of symptoms with no neurologic sequelae. CONCLUSION:: Recurrent benign lymphocytic aseptic meningitis is recognized in this SLE patient. We propose that noninfectious Mollaret meningitis be classified as a feature of neuropsychiatric SLE syndromes.
Journal: Neurologist. 2008 Jan;14(1):43-45.
Authors: Wright SE, Shaikh ZH, Castillo-Lugo JA, Tanriover B.
Department of Pharmacy, Methodist Dallas Medical Center, Dallas, Texas, USA.
Immune globulin intravenous (human) (IGIV) is effective in the treatment of various autoimmune and inflammatory disorders. Recently, high-dose IGIV 2 g/kg has been utilized in the treatment of antibody-mediated rejection in solid organ transplantation. We report a renal transplant recipient who developed aseptic meningitis and diplopia from abducens nerve (cranial nerve VI) palsy following IGIV administration for antibody-mediated rejection. Potential mechanisms of the IGIV-related aseptic meningitis are elaborated. Clinicians should be aware of aseptic meningitis and cranial nerve palsy as an adverse reaction to IGIV exposure and monitor for its signs and symptoms.
Journal: Transpl Infect Dis. 2007 Dec 12
Authors: Dalal A, Likhi R.
Division of Infectious Diseases, New York Hospital Queens, 56-45 Main Street, Flushing, NY 11355, USA. tsiacmed@yahoo.com
Corynebacterium minutissimum, the causative agent of erythrasma, is a gram-positive, non-spore forming, aerobic or facultative anaerobic bacillus. It has rarely been associated with extracutaneous disease, since its description in 1961. A computerized medline search for review of literature was performed. To our knowledge, there have been 18 cases of C. minutissimum infections that caused conditions other than erythrasma. These include reports of cases of abscess formation, intravascular catheter-related bacteremias, ophthalmologic involvement, endocarditis, peritonitis, cutaneous granulomas, pyelonephritis in an infant and primary bacteremia with underlying hematologic malignancy. We report a rare case of bacteremia and meningitis due to C. minutissimum successfully treated with intravenous ampicillin.
Journal: J Infect. 2008 Jan;56(1):77-9. Epub 2007 Nov 26.
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