Literature DB >> 35846899

Subdural empyema due to mixed infections successfully treated medically: A case report with review literature.

Mostafa Meshref1, Anas Zakarya Nourelden2,3, Alaa Ahmed Elshanbary3,4, Yossef Hassan AbdelQadir3,4, Mohamed Sayed Zaazouee3,5, Khaled Mohamed Ragab3,6, Eman Mohammed Sharif Ahmed7, Sarya Swed8.   

Abstract

Subdural empyema is a rare intracranial infection with an accumulation of purulent material between the dura and arachnoid matter. We report a case of 17 years old presented with an altered conscious level. CSF analysis showed increased WBCs. His situation has improved after treating by acyclovir, ceftriaxone, vancomycin, and dexamethasone.
© 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.

Entities:  

Keywords:  bacterial infection; medical treatment; meningeal irritation; subdural empyema; viral infection

Year:  2022        PMID: 35846899      PMCID: PMC9280757          DOI: 10.1002/ccr3.6049

Source DB:  PubMed          Journal:  Clin Case Rep        ISSN: 2050-0904


INTRODUCTION

Subdural empyema (SDE) is a collection of pus between the dura and arachnoid layers of the meninges. It is a rare infection of the brain, and it is an almost fatal condition if left untreated, but since using antibiotics, the mortality rate has decreased and now ranges from 14% to 28%. , In infants, it complicates neonatal meningitis, but in older children, it develops mainly due to ear, sinus infection, or spread from a hematogenous source. , , , , , , In males, SDE is more frequently seen in males, and it is the most commonly encountered intracranial complication of infection. , The patient usually presents with fever, sinusitis, and neurological deficits with less frequent symptoms, including headache and seizures with alteration of the level of consciousness. , , , , , Laboratory investigations vary from blood to imaging. Computed tomography (CT) and magnetic resonance imaging (MRI) are the most important. , Also, white blood cell count, erythrocyte sedimentation rate, and C‐reactive protein level may be helpful. Imaging is recommended for every patient suspected to have a subdural abscess. In some cases, when the diagnosis by CT and MRI is unclear, hollow screws have a diagnostic value. Road spectrum antibiotics are usually the first‐line management, and they may be enough to control the infection. , , However, the surgical intervention must be considered if the antibiotics fail to maintain or other surgery indications. , The most common surgical procedures are craniotomy and burr holes. , If the surgical intervention has been done within 72 h, the chance for disability is 10% compared to 70% when done after 72 h. Because of its rarity, many doctors may not have seen a case in recent years. The topic should be re‐visited to remind them to be aware of it. Also, it is difficult to distinguish from meningitis; hence, the attending clinician must have a high suspicion index. In this report, we presented a SDE case successfully treated by medical treatment in our hospital. Also, we systematically summarized the previously published case reports about SDE.

LITERATURE REVIEW

We searched for published case reports in four electronic databases: PubMed, Scopus, Web of Science, and Cochrane Central Register of Controlled Trials (CENTRAL) in October 2020 using the following query: (“Empyema, Subdural”[Mesh]). We included all English case reports about SDE in adolescent patients (10–19 years). Since 1990, approximately 35 studies with 53 patients have reported similar cases in this age group; almost all were males (86.7%). The observed pattern of predisposing events is sinusitis, otitis media, or an upper airway infection. Patients have usually suffered from fever, headache, and drowsiness. The neurological manifestations started with nuchal rigidity (17% of cases), hemiplegia (11.3% of cases), or seizures (18.8% of cases). Details of each case and the organism isolated from the culture and the outcome are shown in Table 1.
TABLE 1

Summary of the previous case reports , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,

Study IDSexAgePredisposing eventSigns and symptomsBilateral or unilateralLocationSpecific locationMedline ShiftIntra‐axial component (yes/no)CNS infection (causative organism)Follow‐up periodIntervention usedOutcome
Şahin 2015Male16SinusitisProjectile vomiting, lethargy, fever, and headacheUnilateralSubduralAround the right cerebral hemisphere then relapse in the posterior interhemispheric fissurePresentNone Streptococcus constellatus 2 monthsFrontoparietal craniotomyHemiparesis of the patient improved gradually and SDE regressed completely after ampicillin treatment
Yu ¨cel 1998Male14Upper air way infectionDeterioration of consciousness, right hemiparesis, edema in the left eyelid and seizuresUnilateralSubduralFrontalAbsenceNone Streptococcus pneumococcus 2 weeksCraniectomyPatient lost vision then he responded for treatment and was released from hospital
Arifianto 2017Male17Allergic rhinitisDeterioration in consciousness, difficulties in speech, and hemiparesisUnilateralSubduralInterhemispheric and infratentorialPresentNone Staphylococcus epidermidis 4 weeksConservative therapy then craniotomyAll the symptoms resolved; the only remaining symptom was limited extraocular muscle movement
Balfour‐Lynn 1997Female16Seizure and visual hallucinationUnilateralSubdural empyemaOver the right cerebral hemisphereAbsenceYes Burkholderia cepacia 1 yearCraniectomyInitial recovery then deterioration and obliterative bronchitis of the lung although the use of antibiotics
Banerjee 2010Male12Exposure to an active case of pulmonary tuberculosisRaised intracranial pressure and fever for 1 month and altered sensorium for 2 daysUnilateralSubdural empyemaLeft frontoparietal and interhemisphericAbsenceNoAcid‐fast bacilli of TB18 monthsCraniectomyFull recovery and no recurrence
Derin 2015Male16Dental infectionDental and facial pain and swelling of the left faceUnilateralSubdural empyemaFrontalAbsenceNo Streptococcus viridans 8 weeksSinus drainage for pansinusitis and Empiric therapyRecovery and patient discharge
Borovich 1990All of them are males

Case 1: 17

Case 2: 35

Case 3: 58

Case 1: purulent meningitis

Cases 2 & 3: acute meningitis

Case 1: headaches, abdominal pain, and fever of 1 month's duration

Case 2: 1 day of headaches and fever

Case 3: otorrhea, fever, and headaches

Cases 1 & 2: unilateral

Case 3: Bilateral

All of them are subtentorial collection with marked mass effectAll cases: AbsenceAll cases: No

Case 1: Pneumococcus and Proteus.

Cases 2 & 3: None mentioned

Case 1: penicillin and gentamicin then left suboccipital craniectomy

Case 2: Antibiotics then suboccipital craniectomy

Case 3: penicillin and chloramphenicol then external ventricular drainage, drainage of the subtentorial pus, and a bilateral mastoidectomy

Cases 1 & 2: Recovery and patient discharge

Case 3: The patient died 24 h after surgery

Calik 2012Male13Upper air way infectionFever and cervical micro lymphadenopathyUnilateralSubdural empyemaFrontalAbsenceNo4 weeksCraniotomy and sinusotomyRecovery and patient discharge
Conlon 1996Case 116Fever and left frontal headache then seizuresUnilateralSubdural empyemaFrontalAbsenceNoNRCraniotomyRecovery and patient discharge
Female16Upper air way infectionPhotophobia, frontal headache and periorbital swellingUnilateralCerebritisFrontalAbsenceNoPansinusitis by B hemolytic Streptococcus group A1 weekPus aspiration from sinusRecovery and patient discharge
Dolan 1995Male16Suspected sinusitisAltered mental status and slurring of speechUnilateralSubdural empyemaFrontalAbsenceNoNRNRCraniotomy and twist drill ventriculostomyRecovery and patient discharge
Dunn 2013Male14Migraine headaches and acute sinusitisVomiting and nauseaUnilateralEpidural and subdural empyemaFrontopaetialPresentNoThreatening6 weeksBifrontal craniotomy, physical and speech therapies in follow‐upFull recovery and no recurrence
Harris 1987Male12SinusitisFever, lethargy and monoplegiaUnilateralSubdural empyemaAbsenceNoNRNRCraniotomyRecovery and patient discharge
Heilbronn 1984Male13PansinusitisFrontal headache early then the patient developed neck stiffnessUnilateralSubduralFrontal and temporalAbsenceNoPansinusitis by B hemolytic Streptococcus group ANRExploration surgery and resection of necrotized tissuePatient death
Female12PharyngitisFever, neck stiffnessUnilateralSubdural empyemaLateral ventriclesAbsenceNoNRCraniectomyRecovery and patient discharge with anticonvulsant therapy
Holland 2012Male15SinusitisHeadache and low‐grade fever then motor disabilityUnilateralSubdural empyemaRight frontal sinusPresentNo Pneumococcus 6 monthsCraniotomy, ventricular drain, speech, and physical therapyPostsurgical facial droop and unequal pupil dilation, after recovery the patient was discharged with residual left‐sided weakness
Jones 1997Female14Previous infection of mixed coliforms and EnterococcusDeterioration of consciousness and bilateral abducent nerve palsyUnilateralSub‐tentorial empyemaLeft cerebellar hemisphereAbsenceNo Enterococcus faecalis 4 weeksCraniectomy and radical mastoidectomyFull recovery and no recurrence
Kageyama 2000Male18Neurological deterioration, mild fever and vomitingUnilateralSubdural empyemaParanasal sinuses and convexityAbsenceNo Streptococcus milleri 2 weeksBurr holes drainage and barbituratesRecovery and patient discharge
Kuczkowski 2005Male14Purulent rhinorrhea and upper respiratory tract infectionHeadache, nausea, vomitingBilateralSubdural empyemaFrontal brain lobesAbsenceNoβ‐hemolytic group C Streptococcus CraniotomyFull recovery and no recurrence
Male12Purulent rhinorrhea and upper respiratory tract infectionHeadache, periorbital swelling and meningitisUnilateralSubdural empyemaFrontal sinusesAbsenceNoNegativeCraniotomyDeath 13 days after surgery
Kwangong 2002All are males7 patients (9–14)SinusitisHeadache, fever, motor deficit, seizures, and altered mental statusUnilateralSubdural empyemaFrontal sinusitisAbsenceNoCraniotomies and endoscopic sinus surgeries5 complete recovery and 1 hydrocephalus
Lefebvre 2009Male15SinusitisHeadache and hemiparesisUnilateralSubdural empyemaSubdural and maxillary sinusAbsenceNo Streptococcus constellatus 6 monthsCraniotomyRecurrent interhemispheric empyema then total recovery
Manjila 2017Male14SinusitisEpistaxis due to suspected carotid artery damageUnilateralSubdural empyema and cavernous sinus pseudo aneurismFrontal and temporal regionsAbsenceNoMethicillin‐sensitive Staphylococcus aureus Craniotomy and arterial resection and reconstructionRecovery and patient discharge
Martins 2014Male18SinusitisDysarthria, fever and purulent rhinorrheaUnilateralSubdural empyemaMaxillary sinus and frontal sinusAbsenceNoAlpha hemolytic streptococci3 monthsCraniotomy and maxillary antrostomyRecovery and improvement of dysarthria
Millar 1996Male14Flu‐like illnessHemiparesis, headache and feverUnilateralSubdural empyemaRight frontalAbsenceNo2 weeksCraniotomyDeath 3 days after surgery
Mitsuoka 1995Male14Retrobulbar pain and eye swellingSeizure and loss of consciousnessUnilateralSubdural and interhemispheric empyemaFalxAbsenceNO Streptococcus species4 weeksCraniotomyFull recovery and no recurrence
Morgan 1995Male17Dysarthria, headache and neck stiffness and decreased sensationBilateralBasal cisterns and subduralAbsenceNOAnaerobic hemolytic streptococci3 drainage operations yet he developed meningitis and his condition deterioratedDeath after complications
Male15Chronic otitisBilateral papilledema, nystagmus, ataxia, and photophobiaUnilateralSubdural empyemaAbsenceNONonhemolytic streptococciCraniectomy and radical mastoidectomyrecovery and discharge
Male17Postnasal discharge, fever and retroorbital pain, later he developed limb weaknessUnilateralSubdural empyemaAbsenceNOBeta hemolytic streptococci of Lancefield group C4 weeks2 craniotomiesFull recovery and no recurrence
Nica 2011Male15Meningio‐encephalitisDrowsiness, cervical pain and headacheUnilateralSubdural empyemaFronto‐temporo‐parietalAbsenceNO Fusobacterium varium, Fusobacterium mortiferum and Propionibacterium propionicum 1.5 yearsCraniectomyFull recovery after physical therapy
Ong 2002Male13Fever, drowsiness, headaches, and nausea later he developed unequal pupils and a suspected hemorrhagic infarct on CT scanUnilateralSubdural empyemaAbsenceNO Streptococcus constellatus CraniectomyRecovery and patient discharge
Pattisapu 2008Male11Otitis media and mastoiditisNuchal rigidity, headache and lethargyBilateralSubdural empyemaSubtentorialAbsenceNo Proteus, E. coli and Bacteroides 48 monthsBurrhole catheter drainageRecovery and patient discharge
Male11meningitisSeizures, nuchal rigidity and decorticate posturingBilateralSubdural empyemaSubfrontal, parafalcineAbsenceNo Salmonella Type C45 monthsBurrhole catheter drainageRecovery and patient discharge
Female13Ethmoiditis and frontal osteomyelitisFacial swelling, orbital cellulitis and hemiparesisBilateralSubdural empyemaParafalcineAbsenceNoGroup D Streptococcus, Bacteroides melaningenicus 38 monthsCraniotomy and ethmoidectomyRecovery and patient discharge
Sengul 2009Male15Left otitis media and meningitisFever, headache, earache, and neck stiffnessUnilateralSubdural empyemaAbsenceNoNo organisms on culture2 yearsCraniectomyRecovery and patient discharge
Per 2010Male15Facial swelling and fever later, he developed hemiparesis and seizuresUnilateralEpidural and subdural empyemaFrontalAbsenceYes Pasteurella multocida 4.5 yearsEmpyema evacuationRecovery and the patient is kept on antiepileptic therapy
Salunke 20104 males and 2 females6 patients (12–19)All presented with headache, vomiting, and fever only one patient had advance seizures and hemiparesisUnilateralSubdural empyemaFront parietal subduralAbsenceNo4 Negative cultures ‐1 MRSA ‐1 E. coli 3–60 monthsCraniotomyRecovery and discharge
Tankhiwale 2014Male14High grade intermittent fever, altered sensorium, neck stiffness, and seizuresBilateralSubdural empyemaSubduralAbsenceNo Mycobacterium fortuitum 6 weeksCraniotomyFull recovery and no recurrence
Teelin 2017Male14SinusitisSeizures, headache, intermittent low‐grade feverUnilateralSubdural empyemaFrontalAbsenceNo Streptococcus anginosus CraniotomyFull recovery and no recurrence
Teng 2012Male17Sore throatFever, nuchal rigidity and drowsinessUnilateralEpidural and subdural empyemaFrontoparietal subdural and medial‐frontal epiduralAbsenceNo Fusobacterium speciesCraniotomyFull recovery and no recurrence
Waseem 2008Male14Upper air way infectionFever and headaches, later he developed deep dull ache and facial heavinessUnilateralSubdural empyemaFrontal and ethmoid sinusesAbsenceNoGroup F streptococci2 monthsCraniotomyRecovery and discharge
Westhout 2007Male16Sore throatDyspnea, neck pain, anorexia and oliguriaBilateralSubdural empyemaAbsenceNo Streptococcus species7 weeksConservative treatment after tonsillectomyRecovery and discharge
Summary of the previous case reports , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Case 1: 17 Case 2: 35 Case 3: 58 Case 1: purulent meningitis Cases 2 & 3: acute meningitis Case 1: headaches, abdominal pain, and fever of 1 month's duration Case 2: 1 day of headaches and fever Case 3: otorrhea, fever, and headaches Cases 1 & 2: unilateral Case 3: Bilateral Case 1: Pneumococcus and Proteus. Cases 2 & 3: None mentioned Case 1: penicillin and gentamicin then left suboccipital craniectomy Case 2: Antibiotics then suboccipital craniectomy Case 3: penicillin and chloramphenicol then external ventricular drainage, drainage of the subtentorial pus, and a bilateral mastoidectomy Cases 1 & 2: Recovery and patient discharge Case 3: The patient died 24 h after surgery

CASE REPORT

A 17‐year‐old male patient was referred to our hospital. He had no history of co‐morbid illnesses. At first sight, he seemed distracted, and an altered conscious level was noted. By history, 7 days ago, the condition was started with a headache and low‐grade fever without apparent septic focus; no tonsillitis or upper respiratory tract infection. The patient came to our hospital with his family member (from whom the history had been taken). They complained that the patient had a fever, which was not improved by analgesics associated with malaise and disturbing consciousness level in drowsiness and confusion; the patient was inattentive and disoriented to time, place, and persons. On examination, the patient was feverish (38.5), drowsy, confused, and had no focal neurological deficit with positive meningeal irritation signs, neck stiffness, positive kerning's, and stretch leg signs. CT brain at once showed mild diffuse brain edema of the right cerebral hemisphere with a suspected thin rim of overlying extra‐axial fluid collection (Figure 1). We asked for a lumbar puncture (after taking consent from the family) to obtain a CSF sample for analysis. Septic screen samples, urine analysis and cultures, nasal swab, axillary culture, throat culture, blood culture, and sputum culture were also withdrawn. Routine laboratories were withdrawn as well, including complete blood count with differential, kidney and liver functions, and electrolyte levels.
FIGURE 1

CT brain at presentation: mild diffuse brain edema of the right cerebral hemisphere

CT brain at presentation: mild diffuse brain edema of the right cerebral hemisphere Few days later, the results of CSF analysis showed that CSF was clear colorless fluid, RBCs 400 cells/cmm, WBCs 66 cells/cmm (neutrophils 30%, lymphocytes 65%, mononuclear cells 5%), CSF glucose was 4.8 mmol/L which is high (normal range 2.2–3.9 mmol/L), CSF protein was 52.7 mg/dl which is also high (normal range 15–45 mg/dl). Also, CSF cultures were negative for any bacterial growth, including gram bacteria and acid‐fast bacilli. Acid‐fast bacilli PCR is also negative. Septic screen results also were negative for any bacterial growth. The rest of the tests were normal except for an increased W.B.C.s count of 14 × 103 with increased neutrophils 87.9. Low‐grade fever at first, high glucose level, and predominance of lymphocytes in CSF are evidence of viral infection. In addition, mucocele and the presence of sinusitis are bacterial infections, so a treatment that covers possible causes of C.N.S. infection was initiated: acyclovir (10 mg/kg IV ter in die [tid]; three times a day), ceftriaxone (2 g IV bis in die [bid]; twice a day), vancomycin (750 mg IV bid), and dexamethasone (4 mg IV quarter in die [qid]; four times a day). The following day, an MRI brain with contrast was conducted and showed mild diffuse thickening of the pachy/leptomeninges overlying the right cerebral hemisphere with mild intervening fluid collection seen eliciting low signal on t1 and high signal on t2‐weighted images with evidence of diffusion restriction, features suggestive right‐side meningitis with mild SDE. Evidence of right‐sided mild mass effects that was manifested by effacement of the underlying cortical sulci with mild compression on the right lateral ventricle. In addition to that, there was obliteration and mildly expansion of the frontal sinus, showing a high signal on both t1‐, and t2‐weighted images, likely representing mucocele formation. Also, the sphenoid, right ethmoid sinuses, and suitable mastoid air cells have been destroyed (Figure 2).
FIGURE 2

MRI brain with contrast at the next morning: Mild diffuse thickening of the pachy/leptomeninges over lying the right cerebral hemisphere with mild intervening fluid collection

MRI brain with contrast at the next morning: Mild diffuse thickening of the pachy/leptomeninges over lying the right cerebral hemisphere with mild intervening fluid collection At the end of the second day after admission, the patient developed serial attacks of generalized tonic colonic fits, controlled by giving loading phenytoin (15 mg/kg); after that, we kept him on levetiracetam (500 mg P.O. B.I.D.). Also, E.E.G. was done, which showed slowness in activity (Figure 3). The patient's condition improved on the 5th day regarding consciousness level, and no more fits had occurred. The patient was continued on the same treatment measures. A follow‐up MRI. brain with contrast was done after 1 week (Figure 4) and 3 weeks (Figure 5), which showed significant regression of the meningeal thickening and enhancement for the right SDE.
FIGURE 3

EEG sheet which showed slowness activity

FIGURE 4

MRI brain with contrast during the follow up after 1 week

FIGURE 5

MRI brain with contrast during the follow up after 3 weeks

EEG sheet which showed slowness activity MRI brain with contrast during the follow up after 1 week MRI brain with contrast during the follow up after 3 weeks The patient was discharged with marked improvement up to his normal state with no complaints.

DISCUSSION

This case report presents a patient with SDE resulting from a mixed bacterial and viral infection. The patient suffered from sinusitis 7 days before our investigation. The CSF analysis showed an increasing number of WBCs (66 cells/cmm) and 30% neutrophils. The CT scan showed mild diffuse brain edema of the right cerebral hemisphere with suspected mucocele formation, which is considered evidence of bacterial infection. Also, CSF analysis showed an increase in the number of lymphocytes 65% and glucose 4.8 mmol/L, which is evidence of viral infection. Our case showed a thin rim in CT and no significant midline shift in MRI, so it is considered a mild case. Although surgery is the first line in the treatment of SDE, there is a widely unutilized option to use antibiotics in mild cases. , So we treated our patient medically with acyclovir (10 mg/kg IV tid) for viral infection; ceftriaxone (2 g IV bid) and vancomycin (750 mg IV bid) for bacterial infection and dexamethasone (4 mg qid). The treatment was effective, and the patient had recovered with no severe side effects or disability. What makes this case unique is a mixed infection; the patient was also treated medically, while a limitation was no PCR analysis for causative organisms. The case was diagnosed as SDE depending on the clinical history (fever, disturbed conscious level, meningeal irritation signs, fits, and preceding infection), CSF findings (which showed the proof of mixed infection), and MRI brain findings. Also, there was evidence of EEG changes in the form of slowness activity, which is going with Mauser H.W et al. They found multiple EEG changes that may occur with SDE cases, including diffuse slowness. Thus, diagnosis depends only on clinical history, signs, laboratories, EEG, and radiology findings. Ruth et al. concluded that a nonsurgical strategy might be considered for patients with a good clinical condition with a minor shift from the midline on radiology results. , For 4 weeks, Musa et al. reported evidence of pre‐surgical treatment with I.V chloramphenicol and metronidazole. They increased a Glasgow coma scale from 8/15 to 15/15 with no seizures. SDE had reported getting negative in culture test; a case series by Madhugiri et al. consisting of 27 patients with a mean age of 10 years reported that 26% of patients get negative in culture test. Based on our case, physicians should consider the treatment of viral and bacterial infections in similar circumstances. Medical treatment of mild SDE patients can be effective and safe. Future research is needed to investigate the merits and limitations of using medical therapy alone in SDE with mild and moderate cases. In conclusion, as there were multiple conflicts in differentiation between SDE and meningitis, all attending doctors must suspect it. Start medical treatment as soon as possible for all suspected cases depending on the clinical, radiological, and laboratory findings. According to the case degree, early intervention in those cases, whether medical or surgical, can improve patient outcomes and good prognosis. In spite, our case showed marked improvement only on using medical treatments. Multiple researches should be conducted for clarification and putting criteria for either medical or surgical therapies for SDE patients.

AUTHOR CONTRIBUTIONS

All authors have contributed in writing and reviewing the manuscript.

CONFLICT OF INTEREST

There is no conflict of interest.

ETHICAL APPROVAL

Consent to case study report given by Nassau University Medical Centre, NY.

CONSENT

We obtained all appropriate patient consent forms. In the form, the patient has given his consent for his images and other clinical information to be reported in the journal. The patient knew that his name and initials would not be published, and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed. Written informed consent was obtained from the patient to publish this report in accordance with the journal's patient consent policy.

GUARANTOR

Sarya Swed.
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