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Transcript
Differential diagnosis of aseptic meningitis syndrome
Infectious etiologies
Noninfectious causes


Viruses
 Enteroviruses - Polio, coxsackievirus,
 Nonsteroidal anti-inflammatory drugs
echovirus
 HSV types 1 and 2
 Varicella-zoster virus
 Adenovirus
 Epstein-Barr virus
 LCMV
 HIV
 Influenza virus types A and B

Bacteria
 Partially treated meningitis
 Parameningeal infection
 Endocarditis
 Mycoplasma pneumoniae
 M tuberculosis
 Ehrlichiosis - Monocytic, granulocytic
 Borrelia burgdorferi
 Treponema pallidum
 Brucella species

Fungi
 C neoformans
 Histoplasma capsulatum
 Coccidioides immitis
 Blastomyces dermatitides

Parasites
 Toxoplasma gondii
 Taenia solium (cysticercosis)
 Sarcoidosis
 Leptomeningeal cancer
 Posttransplantation lymphoproliferative
disorder
 Systemic lupus erythematosus
 Wegener granulomatosis
 CNS vasculitis
 Behçet disease
Drugs
(NSAIDs)
 Trimethoprim-sulfamethoxazole, Vaccina-
References:
1. ^ synd/1537 at Who Named It?
2. ^ P. Mollaret. Méningite endothélio-leucocytaire
multirécurrente bénigne. Syndrome nouveau ou maladie nouvelle? (Documents cliniques). Revue neurologique, Paris, 1944, 76: 57-76.
MollaretsMeningitis.org
Support Organization
Informational Pamphlet
tion
 Allopurinol
 Systemic diseases
 Sarcoidosis
 amoxicillin
 OKT3
 Azathioprine
 Intravenous immunoglobulin
 Isoniazid
 Intrathecal methotrexate
 Intrathecal cystine arabinoside

4. ^ Mollaret's meningitis at patient.co.uk
5. http://emedicine.medscape.com/article/1169489overview
(Recurrent Viral/Aseptic Meningitis)
Mollaret's
Systemic diseases
 Sarcoidosis
 Leptomeningeal cancer
 Posttransplantation lymphoproliferative disorder
 Systemic lupus erythematosus
 Wegener granulomatosis
 CNS vasculitis
 Behçet disease
 Vogt-Koyanagi-Harada syndrome

3. ^ Tarakad S Ramachandran, MBBS, FRCP(C),
FACP (Feb 12, 2010). "Aseptic Meningitis". Emedicine. http://emedicine.medscape.com/article/1169489overview. Retrieved 9 January 2011.
Miscellaneous
 Arachnoiditis
 Migraine
Postinfectious syndromes
Mollaret’s
Meningitis Support
Organization
~Daily Support Designed to HELP
Mollaret's Meningitis Sufferers
HTTP://
MOLLARETSMENINGITIS.ORG
Meningitis
Mollaret’s Meningitis
WHAT IS MOLLARET’S MENINGITIS?
Diagnosis
Drug-induced aseptic meningitis
Signs / Symptoms / Diagnosis
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.
The incidence of drug-induced meningitis (DIAM)
is unknown. Many antimicrobials, such as
trimethoprim-sulfamethoxazole, ciprofloxacin,
cephalexin, metronidazole, amoxicillin, penicillin,
and isoniazid, are causes of aseptic meningitis. In
addition, the xanthine oxidase inhibitor allopurinol
has been implicated in causing aseptic meningitis.
DIAM is a complication in which numerous other
drugs, namely nonsteroidal anti-inflammatory
drugs (NSAIDs), ranitidine, carbamazepine, vaccines against hepatitis B and mumps, immunoglobulins, OKT3 monoclonal antibodies (ie, directed against the T3 receptor and, therefore, pan
T-cell antibodies), co-trimoxazole, radiographic
agents, and muromonab-CD3, also have been associated. A high index of suspicion is needed to
make an accurate diagnosis of DIAM. Diagnostic
accuracy in clinical care depends on a complete
history and physical examination.
Mollaret's meningitis is a rare form of recurrent meningitis originally described by Mollaret in 1944. According to
Bryun, who further refined the clinical diagnostic criteria,
the condition is characterized by (1) recurrent episodes
of severe headache, meningismus, and fever; (2) CSF
pleocytosis with large endothelial cells (ie, Mollaret
cells), neutrophils, and lymphocytes; (3) recurrent attacks separated by symptom-free periods of weeks to
months; (4) spontaneous remission of symptoms and
signs; and (5) no known causative agent. Cases without
fever, with increased CSF gamma globulin and transient
neurological signs and symptoms, have been reported.
Transient neurological abnormalities, including seizures,
diplopia, pathologic reflexes, cranial nerve pareses, hallucinations, and coma, occur in as many as 50% of patients.
Mollaret cells, considered by many to be the hallmark
of Mollaret meningitis (although not pathognomonic), are
observed early and may comprise 60-70% of cells in the
CSF. These cells are usually present for only the first 24
hours and can be missed easily. After the first 24 hours,
the CSF shows a lymphocytic
predominance with cell counts
usually less than 3000/mm3.
Hypoglycorrhachia (ie, low CSF
glucose concentration) is reported in one third of the paMollaret’s Cell
tients. CSF protein usually is
elevated mildly. Recent data
suggest that HSV-2 and, less frequently, HSV-1 may be
etiologic in some if not most cases of Mollaret's Meningitis. Hence, acyclovir (intravenous or oral) or valacyclovir
(oral only) are worthy of consideration for both therapy
and prophylaxis.
Mollaret's Meningitis is suspected based on clinical
criteria and confirmed by HSV 1 or HSV 2 on PCR of
CSF, although not all cases test positive.
Aseptic meningitis syndrome is not caused by pyogenic bacteria, but can be caused by multiple conditions including infectious viral and nonviral causes
and many noninfectious etiologies. Hence, this term
is no longer synonymous with viral meningitis, although the two often are used interchangeably.
The clinical presentation does not help in differentiating DIAM from
infectious meningitis.
The CSF profile (ie, neutrophilic pleocytosis)
does not allow DIAM to
be distinguished from
infectious meningitis.
Systemic lupus erythematosus is the single most frequent underlying
condition associated with DIAM. Recurrent DIAM
is well known; females usually predominate, and
the frequency varies with the different underlying
conditions.