|Purulent Meningitis as an Unusual Presentation of Staphylococcus aureus Endocarditis: A Case Report and Literature Review.|
|Jump to Full Text|
|PMID: 21541188 Owner: NLM Status: PubMed-not-MEDLINE|
|On presentation of Staphylococcus aureus endocarditis, unusual manifestations may represent the main clinical features of the disease. Isolated bacterial meningitis as the first manifestation of endocarditis is considered to be an unusual neurological complication. Here, we describe a case S. aureus endocarditis presenting as isolated meningitis and mimicking meningococcal septicaemia. Because of the high mortality rate of the disease, the prompt recognition of this infectious syndrome is of crucial importance for the correct management of patients.|
|Giancarlo Ceccarelli; Gabriella d'Ettorre; Vincenzo Vullo|
Related Documents :
|9654838 - Spinal accessory nerve palsy as a cause of pain after whiplash injury: case report.
19886118 - Herpes zoster brachial plexopathy with predominant radial nerve palsy.
16420398 - Adult abdominal migraine: a new syndrome or sporadic feature of migraine headache? a ca...
17456098 - Importance of electromyography and the electrophysiological severity scale in forensic ...
18637978 - Postmortem changes of human bodies on the bathyal sea floor--two cases of aircraft acci...
8041888 - Surveillance of poliomyelitis in the united kingdom.
|Type: Journal Article Date: 2011-03-28|
|Title: Case reports in medicine Volume: 2011 ISSN: 1687-9635 ISO Abbreviation: Case Rep Med Publication Date: 2011|
|Created Date: 2011-05-04 Completed Date: 2011-07-14 Revised Date: 2013-02-21|
Medline Journal Info:
|Nlm Unique ID: 101512910 Medline TA: Case Rep Med Country: United States|
|Languages: eng Pagination: 735265 Citation Subset: -|
|Department of Public Health and Infectious Diseases, University of Rome "Sapienza", 00155 Rome, Italy.|
|APA/MLA Format Download EndNote Download BibTex|
Journal ID (nlm-ta): Case Report Med
Journal ID (publisher-id): CRIM
Publisher: Hindawi Publishing Corporation
Copyright © 2011 Giancarlo Ceccarelli et al.
Received Day: 10 Month: 10 Year: 2010
Revision Received Day: 17 Month: 1 Year: 2011
Accepted Day: 27 Month: 1 Year: 2011
Print publication date: Year: 2011
Electronic publication date: Day: 28 Month: 3 Year: 2011
Volume: 2011E-location ID: 735265
PubMed Id: 21541188
|Purulent Meningitis as an Unusual Presentation of Staphylococcus aureus Endocarditis: A Case Report and Literature Review|
|Department of Public Health and Infectious Diseases, University of Rome “Sapienza”, 00155 Rome, Italy
|Correspondence: *Giancarlo Ceccarelli: firstname.lastname@example.org
[other] Academic Editor: Niranjan Kissoon
Staphylococcus aureus is a leading cause of bacteraemia and endocarditis, but also a rare cause of bacterial meningitis. The mortality rate of S. aureus endocarditis is approximately 20–40%, depending on the extreme variability in clinical presentation which may delay the early diagnosis and treatment of the disease [1–3]. Therefore, early diagnosis and adequate monitoring of the various complications due to S. aureus endocarditis are important. In this paper, we describe a case of S. aureus endocarditis presenting as isolated meningitis and mimicking meningococcal septicaemia.
A 40-year-old male was hospitalized following 5 days of fever, lethargy, and mental confusion. He had been taking antipyretics and Amoxicillin + Clavulanic acid 1 g 2 times/daily as prescribed by a physician for 5 days without any benefits. From his medical history, there was no evidence of previous neurological, respiratory, cardiovascular, gastrointestinal, and renal disorders. On admission, the patient was lethargic and mentally confused. His vital signs were as follows: body temperature 39.4°C, blood pressure 100/60 mmHg, heart rate 112/min, and respiration rate 32/min. Physical examination revealed photophobia and nuchal rigidity. Kernig's sign and Burdizinski's signs were both positive. There were no abnormal findings in the cardiovascular, respiratory, and gastrointestinal system. Laboratory studies were as follows: white blood cells (WBC) 23.4 × 103/mmc with 93% neutrophils and 3% lymphocytes; red blood cells (RBC) 4.2 × 106/mmc; haemoglobin (Hb) 11.6 g/dL. There were no alterations of renal and hepatic function; electrolytes and glycaemia were within normal values; erythrocyte sedimentation rate was 82; C-reactive protein 7 mg/dL. Coagulation data demonstrated INR 1.29 ratio, fibrinogen: 964 mg/dL; fibrin split products: 1169 μg/mL. Chest X-ray did not show alteration. ECG examination showed typical findings of tachycardia with a regular rhythm. Computed tomography (CT) scan of the brain was negative for space-occupying lesions and intracranial hypertension. 30 minutes after admission into hospital a lumbar puncture was performed and cerebrospinal fluid (CSF) findings showed opalescent CSF with WBC 962/mmc (90% neutrophils and 10% lymphocytes), glucose 70 g/dL, protein 105 g/dL, and CSF Gram stain smears negative. Within 4 hours from admission, there was evidence of septic shock with diffuse pustular purpuric lesions. Based on the CSF findings as well as systemic signs, a presumptive diagnosis of meningococcal sepsis was made and ceftriaxone (2 g every 12 hours I.V.) was administered. 48 hours after admission, the patient still had fever and WBC were 19.4 × 103/mmc with 87% neutrophils. After 3 days from admission, physical examination revealed abdominal tenderness and pain, and showed a 2-3/6 systolic ejection murmur at the left sternal border proceeding to neck blood vessels. Therefore, transthoracic echocardiography was performed; it revealed a vegetation adherent to the posterior leaflet of the mitral valve with mitral regurgitation consistent with mitral valve endocarditis; these findings were confirmed by transesophageal echocardiography.
A following total body CT scan showed multiple splenic spots compatible with abscesses and one small abscess on left psoas muscle. Moreover a methicillin sensitive S. aureus (MSSA) was isolated in two blood cultures collected on the first day from admission, while the CSF cultures were negative. Based on these findings, on the third day of admission, antibiotic therapy was changed to oxacillin (2 g I.V. every 4 hours) plus gentamicin (1 mg/kg I.V. every 8 hours). One week after the beginning of the new therapy, the patient showed a progressive defervescence, reduction of abdominal pain and skin lesions, nuchal rigidity and lethargy slowly resolved, the leukocyte count had reduced considerably, and all blood cultures were negative. The transthoracic echocardiogram showed a reduction of the vegetation on the mitral valve. A total body CT scan was repeated after 10 days of treatment and it excluded the presence of embolism; it also showed a reduction of the splenic and psoas muscle abscesses. After 6 weeks of therapy with Oxacillin and Gentamicin, the patient was free of symptoms and blood plus instrumental examinations showed absence of the previous findings. The patient later had a checkup involving full blood examinations, transthoracic and transesophageal echocardiography, 1 month and 3 months after discharge from hospital, these all showed absence of disease and a total body CT scan done at the end of the 3 months followup was also negative; the patient was therefore considered disease-free and was committed to a cardiologist for monitoring mitral regurgitation and heart function.
Serious S. aureus infections caused by both resistant and susceptible strains are increasingly reported in community and hospital settings . In particular, infective endocarditis represents the most serious S. aureus bacteraemia complication. S. aureus is a unique pathogen because of its ability to cause endocarditis often involving previously architecturally normal cardiac valves. S. aureus endocarditis also can have profound and devastating neurologic consequences. The frequency of neurological complications due to endocarditis was found to remain constant despite therapeutic advances and profound epidemiological changes . Jorge et al.  studied a 222 patients cohort with infective endocarditis: 17 patients presented meningitis as unique manifestation of neurological complication associated to the diagnosis of infective endocarditis, 56 patients presented neurological complication, and the others were without any neurological complication. Also Brouwer et al. reported that 89% of patients with community-acquired S. aureus meningitis at the admission in the hospital had foci of infection outside the central nervous system . The incidence of neurologic complications of infective endocarditis is dependent on the organism and valvular location; the highest incidence is 87% with S. aureus vegetations on the mitral valve. Jorge et al. described that patients with concomitant S. aureus meningitis and endocarditis had a higher mortality (56%) related to age, shock, and infection with phage type 95 strains . Fong and Ranalli reported that meningitis associated with endocarditis caused by S. aureus showed a more fulminant course . Comparative analysis showed a greater mortality rate in presence of neurological complications and meningitis, and S. aureus was the predominant etiological agent .
The risk of occurrence of stroke, hemorrhage in CNS, purulent meningitis, and brain abscess exists in patients with infective endocarditis; anyway their clinical manifestations are often indistinguishable from those present in the same diseases in the absence of endocarditis. Embolic events or autoimmunity may underlie the etiology of stroke but the cause of CNS hemorrhage in infective endocarditis is not completely clear and nearly 30% of hemorrhagic cases are due to staphylococci. Also nonfocal symptoms or encephalopathy can be the result of microscopic emboli and subsequent ischemia. Pathological findings evidence that macroscopic brain abscesses are rare but microscopic abscesses are more common and often are discovered at autopsy. Due to the fact that clinical manifestations are often indistinguishable from those present in the same diseases in the absence of endocarditis, it is useful to consider the possibility of concomitant infection of a heart valve in case of presence of fever, alteration of inflammatory markers, and/or S. aureus bacteremia. Anyway mental status changes, amnesia, nonfocal symptoms, transient ischemic attack-like, and fluctuating focal neurologic signs can herald a diagnosis of infective endocarditis [10–14].
Neuropsychiatric symptoms may be the first manifestation of an underlying cardiac disease. A study by Bademosi et al. indicated that 38% of patients with infective endocarditis had neuropsychiatric manifestations and this may also occur in S. aureus endocarditis . Laboratory and imaging studies of neurologic consequences of endocarditis include cerebrospinal fluid examination, CT of the brain, and magnetic resonance imaging (MRI) that can reveal focal areas of ischemia even in the absence of clinical manifestations of a CNS disorder. Patients with community-acquired S. aureus meningitis have a WBC count and CSF protein levels usually lower than those with other pyogenic meningitis, and the CSF Gram stain is positive in only 40% of cases [1–3]. Anyway Røoder et al. described that only <2% of patients with S. aureus endocarditis developed acute bacterial meningitis with positive CSF cultures . The isolation is more probable from blood cultures than from the CSF [16, 17]. In our case paper, the CSF cultures were negative but the patient had an antibiotic treatment before admission and lumbar puncture. However, in cases of community-acquired bacterial meningitis, any atypical isolate such as S. aureus should be considered suspicious for the presence of another localization of the infection [18, 19].
Spontaneous S. aureus meningitis as a consequence of endocarditis may pass unnoticed initially, because a murmur is absent at presentation in 30% of cases . In our patient, murmur was found during the third day of hospitalization; moreover, skin lesions observed in meningococcal sepsis and in S. aureus sepsis are similar. For that reason, it is important to search for an underlying cardiac cause in patients who present with meningitis and skin lesions in a clinical course that may mimic the classical presentation of meningococcal sepsis. The presence of pustular skin lesions in a patient with sepsis could be suggestive of S. aureus as the pathogenic agent. In fact, in staphylococcal endocarditis purpuric lesions may progress into cutaneous gangrene or may be pustular, with organisms present on Gram stain . However, sometimes other organisms (such as Streptococcus pyogenes, Streptococcus viridians, and Pseudomonas aeruginosa) may be involved in the event of an occasional pustular rush. Morover, although the gonococcal endocarditis is now rare, also Neisseria gonorrhoeae should be considered a possible etiologic agent of endocarditis in the presence of pustular lesions . Microbiologic examination of samples of secretions and biopsies of the petechial rash, purpura, and pustules may be useful for revealing the causative agent. Another two well-known skin manifestations of bacterial endocarditis are Janeway lesions and Osler nodes. Janeway lesions are more commonly seen in acute endocarditis, when bacteria (most often highly virulent organisms such as S. aureus) may be cultured from them and the histology is usually consistent with septic microembolism [22–25].
Distinguishing patients with uncomplicated S. aureus bacteremia from those with endocarditis is therapeutically and prognostically required, but often difficult. The clinical examination and the traditional clinical predictors of endocarditis (as community acquisition, absence of an obvious primary focus and evidence of metastatic foci) in patients with S. aureus bacteremia often fail in establishing a diagnosis of endocarditis . Therefore, echocardiographic evaluation should be considered part of the early evaluation of patients with S. aureus bacteremia [27, 28]. For these reasons, in the last clinical practice guidelines for the treatment of methicillin-resistant S. aureus infections, echocardiography is recommended for all adult patients with bacteremia and transesophageal echocardiography is preferred over transthoracic echocardiography .
In our case, we carried out serial echocardiographic examinations in order to monitor the clinical course of the disease; in fact S. aureus can be a cause of destructive valve endocarditis, and its pathogenic potency is explained by the expression of binding factors promoting the adherence to valves as fibrinogen binding protein . Moreover, we performed both transthoracic echocardiography and transesophageal echocardiography; this is because transesophageal echocardiography is a highly valuable adjunct to other diagnostic tests and would appear to be of benefit in patients with a risk of complicated clinical course who may have additional cardiac lesions not demonstrated by transthoracic echocardiography [31, 32]. In fact, transesophageal exam may be advisable to evaluate perivalvular extension of disease, unsuspected paravalvular abscess, vegetation size, and other factors which may inform surgical decision-making . Staphylococcus aureus infection is associated with a higher recurrence of embolization, and septic embolization has important effect on long-term survival resulting in death in 24% to 50% of those who sustain an embolus . In addition, a significant proportion of patients with endocarditis may also have clinically occult embolic locations: for these reasons we performed serial CT scan examinations in order to monitor the clinical course of embolic complications from endocarditis. Moreover, recently also PET/CT scan has been proposed as an important diagnostic tool for tracing peripheral embolism and metastatic infection in the acute setting of infective endocarditis, since a PET/CT scan detected a clinically occult focus in nearly one third of episodes . In our case the presence of splenic abscess was an important risk factor for rupture of the spleen, because splenic tissue is very fragile (especially if the abscess is located subcapsularly), and a splenic rupture can result from minimal trauma . In these cases, a successful outcome lies with a choice between medical and surgical treatments (splenectomy); however, there is still insufficient evidence in the decision-making process [37, 38].
In summary, S. aureus endocarditis carries a mortality rate of 20–40%: it depends in part on the extreme variability in clinical presentation, which may delay the early diagnosis and treatment of the disease. In case of bacterial meningitis associated to infective endocarditis, the mortality rate approaches to 60% . Isolated bacterial meningitis as the first manifestation of endocarditis is unusual notwithstanding neurological complication . The association of neurological symptoms with skin lesions may mimic the presentation of meningococcal meningitis with septicaemia in absence of classical cardiac signs of S. aureus endocarditis .
In this paper, we emphasize the importance of searching an underlying focus of S. aureus endocarditis in a patient presenting as purulent meningitis and with a presumptive diagnosis of meningococcal sepsis, even in the absence of typical symptoms and/or signs of endocarditis. Because of the high mortality rate of the disease, the prompt recognition of this infectious syndrome is of crucial importance for the correct management of patients.
|1.||Chang FY. Staphylococcus aureus bacteremia and endocarditisJournal of Microbiology, Immunology and InfectionYear: 20003326368|
|2.||Angstwurm K,Halle E,Wetzel K,Schultze J,Schielke E,Weber JR. Isolated bacterial meningitis as the key syndrome of infective endocarditisInfectionYear: 2004321475015007742|
|3.||Kelly J,Barnass S. Staphylococcus aureus endocarditis presenting as meningitis and mimicking meningococcal sepsisInternational Journal of Clinical PracticeYear: 199953430630710563077|
|4.||Korzeniowski OM. Staphylococcus aureus endocarditis in the 21st centuryCurrent Infectious Disease ReportsYear: 2000227928011095866|
|5.||Corral I,Martín-Dávila P,Fortún J,et al. Trends in neurological complications of endocarditisJournal of NeurologyYear: 200725491253125917260173|
|6.||Jorge SC,Medeiros CS,Scuracchio PS,Assef JE,Arnoni AS,Sousa JE. Meningitis and other neurological complications in infectious endocarditisMeningite e outras complicações neurológicas na endocardite infecciosaArquivos Brasileiros de CardiologiaYear: 19925953793831340738|
|7.||Brouwer MC,Keizerweerd GD,de Gans J,Spanjaard L,van de Beek D. Community acquired Staphylococcus aureus meningitis in adultsScandinavian Journal of Infectious DiseasesYear: 200941537537719177261|
|8.||Fong IW,Ranalli P. Staphylococcus aureus meningitisQuarterly Journal of MedicineYear: 1984532102892996463201|
|9.||Jensen AG,Espersen F,Skinhoj P,Rosdahl VT,Frimodt-Moller N. Staphylococcus aureus meningitis: a review of 104 nationwide, consecutive casesArchives of Internal MedicineYear: 199315316190219088250650|
|10.||Røoder BL,Wandall DA,Espersen F,Frimodt-Møoller N,Skinhøoj P,Rosdahl VT. Neurologic manifestations in Staphylococcus aureus endocarditis: a review of 260 bacteremic cases in nondrug addictsAmerican Journal of MedicineYear: 199710243793869217620|
|11.||Bakshi R,Wright PD,Kinkel PR,et al. Cranial magnetic resonance imaging findings in bacterial endocarditis: the neuroimaging spectrum of septic brain embolization demonstrated in twelve patientsJournal of NeuroimagingYear: 199992788410208104|
|12.||Anderson DJ,Goldstein LB,Wilkinson WE,et al. Stroke location, characterization, severity, and outcome in mitral vs aortic valve endocarditisNeurologyYear: 200361101341134614638952|
|13.||Chukwudelunzu FE,Brown RD,Wijdicks EFM,Steckelberg JM. Subarachnoid haemorrhage associated with infectious endocarditis: case report and literature reviewEuropean Journal of NeurologyYear: 20029442342712099929|
|14.||Heiro M,Nikoskelainen J,Engblom E,Kotilainen E,Marttila R,Kotilainen P. Neurologic manifestations of infective endocarditis: a 17-year experience in a teaching hospital in FinlandArchives of Internal MedicineYear: 2000160182781278711025788|
|15.||Bademosi O,Falase AO,Jaiyesimi F,Bademosi A. Neuropsychiatric manifestations of infective endocarditis: a study of 95 patients at Ibadan, NigeriaJournal of Neurology Neurosurgery and PsychiatryYear: 1976394325329|
|16.||Salgado AV,Furlan AJ,Keys TF,Nichols TR,Beck GJ. Neurologic complications of endocarditis: a 12-year experienceNeurologyYear: 19893921731782915785|
|17.||Le Cam B,Guivarch G,Boles JM,Garre M,Cartier F. Neurologic complications in a group of 86 bacterial endocarditisEuropean Heart JournalYear: 19845C971006519094|
|18.||Bayer AS,Seidel JS,Yoshikawa TT,Anthony BF,Guze LB. Group D enterococcal meningitis. Clinical and therapeutic considerations with report of three cases and review of the literatureArchives of Internal MedicineYear: 19761368883886821410|
|19.||Murray HW,Tuazon CU,Sheagren JN. Staphylococcal septicemia and disseminated intravascular coagulation. Staphylococcus aureus endocarditis mimicking meningococcemiaArchives of Internal MedicineYear: 19771377844847879923|
|20.||Plaut ME. Staphylococcal septicemia and pustular purpura. Report of casesArchives of DermatologyYear: 196999182855812462|
|21.||Mansheim BJ. Gonococcal endocarditisSouthern Medical JournalYear: 19807312164516467444561|
|22.||Lin CS,Lee RL,Kuo CM,Lee LC. Positive culture of the Janeway lesion in acute bacterial endocarditisTaiwan Yi Xue Hui Za ZhiYear: 1980791991026929889|
|23.||Gunson TH,Oliver GF. Osler’s nodes and Janeway lesionsAustralasian Journal of DermatologyYear: 200748425125517956487|
|24.||Marrie TJ. Osler’s nodes and Janeway lesionsAmerican Journal of MedicineYear: 2008121210510618261495|
|25.||Silverman ME,Upshaw CB Jr.. Extracardiac manifestations of infective endocarditis and their historical descriptionsAmerican Journal of CardiologyYear: 2007100121802180718082531|
|26.||Nolan CM,Beaty HN. Staphylococcus aureus bacteremia. Current clinical patternsAmerican Journal of MedicineYear: 19766044955001274983|
|27.||Fowler VG Jr.,Li J,Corey GR,et al. Role of echocardiography in evaluation of patients with Staphylococcus aureus bacteremia: experience in 103 patientsJournal of the American College of CardiologyYear: 1997304107210789316542|
|28.||Kern WV. Management of Staphylococcus aureus bacteremia and endocarditis: progresses and challengesCurrent Opinion in Infectious DiseasesYear: 201023434635820592532|
|29.||Liu C,Bayer A,Cosgrove SE,et al. Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and childrenClinical Infectious DiseasesYear: 201152e18e5521208910|
|30.||Wächtler M,Strobel E,Koch U,et al. Native mitral valve endocarditis caused by Staphylococcus lugdunensis in a 22-year-old womanInfectionYear: 200230425125312236574|
|31.||Pedersen WR,Walker M,Olson JD,et al. Value of transesophageal echocardiography as an adjunct to transthoracic echocardiography in evaluation of native and prosthetic valve endocarditisChestYear: 199110023513561864104|
|32.||Kini V,Logani S,Ky B,et al. Transthoracic and transesophageal echocardiography for the indication of suspected infective endocarditis: vegetations, blood cultures and imagingJournal of the American Society of EchocardiographyYear: 201023439640220138467|
|33.||McDonald JR. Acute infective endocarditisInfectious Disease Clinics of North AmericaYear: 200923364366419665088|
|34.||Homma S,Grahame-Clarke C. Toward reducing embolic complications from endocarditisJournal of the American College of CardiologyYear: 200342578178312957420|
|35.||van Riet J,Hill EE,Gheysens O,et al. F-FDG PET/CT for early detection of embolism and metastatic infection in patients with infective endocarditisEuropean Journal of Nuclear Medicine and Molecular ImagingYear: 2010371189119720204357|
|36.||Ebels J,van Elst F,Vanderveken M,et al. Splenic abscess complicating infective endocarditis: three case reportsActa Chirurgica BelgicaYear: 2007107672072318274196|
|37.||Naito R,Mitani H,Ishiwata S,et al. Infective endocarditis complicated with splenic abscess successfully treated with splenectomy followed by double valve replacementJournal of Cardiology CasesYear: 20102e20e22|
|38.||Yoshikai M,Kamachi M,Kobayashi K,Murayama J,Kamohara K,Minematsu N. Splenic abscess associated with active infective endocarditisJapanese Journal of Thoracic and Cardiovascular SurgeryYear: 2002501147848012478868|
Previous Document: A novel animal model of hippocampal cognitive deficits, slow neurodegeneration, and neuroregeneratio...
Next Document: Autologous peripheral blood mononuclear cell recognition of autologous proliferating tumor cells in ...