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Inicio Enfermedades Infecciosas y Microbiología Clínica Spontaneous subdural empyema by Escherichia coli: Case report and literature rev...
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Vol. 34. Núm. 8.
Páginas 531-532 (octubre 2016)
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Vol. 34. Núm. 8.
Páginas 531-532 (octubre 2016)
Scientific letter
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Spontaneous subdural empyema by Escherichia coli: Case report and literature review
Empiema subdural espontáneo por Escherichia coli: descripción de un caso y revisión de la literatura
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4411
Luis Mariano Rojas-Medinaa,
Autor para correspondencia
luismarianorojas@gmail.com

Corresponding author.
, Lucía Esteban-Fernándezb, José Antonio Gutiérrez-Ciercoa, Víctor Rodríguez-Berrocala
a Servicio de Neurocirugía, Hospital Universitario Ramón y Cajal, Madrid, Spain
b Servicio de Neurología, Hospital Universitario Ramón y Cajal, Madrid, Spain
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Tablas (1)
Table 1. Summary of previous cases of spontaneous SE by Escherichia coli.
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Subdural empyema (SE) is defined as a purulent collection between the duramater and arachnoid. The most common pathogenic mechanism is contiguous infection or cranial surgery, being extremely rare an spontaneous presentation,1,2 and the most common etiology is streptococci and staphylococci.3 We present a case of spontaneous SE by Escherichia coli, including a critical literature review.

A 69-year-old man debuted with 48h of 4/5 right hemiparesis and unsteady gait. He had a history of type 2 diabetes mellitus, dyslipidemia and dysuria, ten days before that was labeled as urinary tract infection (UTI) and treated with one dose of fosfomycin. Hemogram showed leukocytosis-neutrophils, elevated C-reactive protein (206mg/L). Unenhanced-CT showed a hypodense left frontoparietal subdural collection (30mm) and midline shift (10mm). On suspicion of chronic subdural hematoma (CSDH), two burr holes were performed, after durotomy, abundant purulent material was obtained, so we made a minicraniotomy to complete the evacuation. Empiric therapy was started with vancomycin (1g/8h), metronidazole (500mg/8h) and cefotaxime (2g/8h); Gram stain was identified Gram-negative bacilli, so vancomycin was suspended, continuing rest of therapy for 5 days until the arrival of culture. E. coli was isolated sensitive to cefotaxime, increasing dose to 2g/6h. The patient presented fever the sixth day, and a 14mm ring enhanced collection was found on the control CT, so a new surgical revision with larger craniotomy was done for evacuation of purulent, and increase of cefotaxim to 4.5g/6h (200mg/kg [90kg]) until 6 weeks. The patient improved until complete recovery, brain MRI after 27 days showed minimal collection. The urine and blood cultures were negative.

SE has a high mortality rate and is associated with severe neurological disabilities. The most common cause is meningitis in children and adjacent infections in adults.3–5 Neurological focal symptoms, leukocytosis and elevated inflammatory reactants are typical. CT and MRI show a subdural collection with contrast ring enhancement, and a restricted diffusion in the diffusion-weighted imaging.

On extensive search in the literature, only 9 cases were found (Table 1): age ranged from 5 months to 91 years, no gender predilection. Six cases presented previous infections, four UTI1,6–8 and two meningitis.2,9 They had history of CSDH (20%) and diabetes mellitus (20%). The most common symptoms were altered mental status and fever (50% each), followed by paresis and headache. Pneumocephalus was observed in 30% at the moment of diagnosis and it has been associated with a worse prognosis.5,7,9 The surgical treatments were burr holes (40%) and craniotomy (30%). Two cases presented recurrences (minicraniotomy 1, burr hole 1), forcing an expanded craniotomy. The mortality was 40%.

Table 1.

Summary of previous cases of spontaneous SE by Escherichia coli.

Case/ref.  Age/sex  Symptoms  Site  Surgery  Recurrence  Outcome  Comments 
1. Kaminogo6  76 y/F  Headache  NA  NA  Satisfactory  UTI by E. coli 
2. Bakker1  88 y/F  Alt.MS, paresis  Burr holes  No  Death  UTI by E. coli. 
3. Miedema2  7 m/F  Fever  NA  NA  Satisfactory  Blood and CSF culture positive for E. coli. 
4. Fender10  5 m/M  Irritability, increased HC  Burr holes/B  Yes. Craniectomy/L  Satisfactory   
5. Nishi8  76 y/F  Fever, Alt.MS  Burr holes  No  Satisfactory  PKD, chronic UTI by E coli. 
6. Bachmeyer9  55 y/M  Fever, Alt.MS  NA  NA  Death  Esophageal cancer treated with Rt and Cht.
Blood and CSF culture positive for E. coli.
CT: pneumocephalus. 
7. Adamides7  91 y/M  Alt.MS, paresis  Craniectomy  No  Death  DM, evacuation CSDH/L 4 months ago.
CT: pneumocephalus.
UTI by E. coli. 
8. Yoon4  79 y/F  Fever, paresis  Burr holes  No  Satisfactory  CSDH/B 15 days ago. 
9. Redhu5  48 y/M  Fever, Alt.MS, Headache  Craniectomy  No  Death  CT: Tension pneumocephalus. 
10. Our case  69 y/M  Dysarthria, paresis  Craniectomy  Yes. Craniectomy  Satisfactory  DM. 

Ref: reference; Sex: F: female, M: male; age: y: years, m: months; symptoms: Alt.MS: altered mental status, HC: head circumference; subdural empyema site: L: left, R: right B: bilateral; comments: UTI: urinary tract infection, PKD: polycystic kidney disease, DM: diabetes mellitus, Rt: radiotherapy, Cht: chemotherapy, CSDH: chronic subdural hematoma; NA: data not available.

Hematogenous spread seems to be the pathophysiological mechanism of spontaneous SE. In 40% of cases presented a distant infection with same germ.1,6–8 Other risk factors for overt infections could be previous CSDH,4,7 diabetes mellitus and immunosuppression states.7,9 In our case, we relate the genesis of spontaneous SE to hematogenous spread of an unconfirmed UTI, in association with diabetes mellitus.

The treatment of choice is surgical evacuation associated to culture adjusted intravenous antibiotics during 4–6 weeks.4,9 The most appropriate surgical approach is still under discussion, as some authors argue that the burr holes are sufficient for evacuation; others suggest that wider exposure as a craniotomy is more effective.3 Yilmaz et al.3 presented a lower recurrence rate on craniotomies (10%) vs. burr holes (38%). In cases with difficult pus extraction, as in multiloculated collections,4 parafalcine location3 and recurrences, is better to carry out a wide craniotomy. Both surgical techniques must perform thorough washing until clear liquid outlet, take care to remove the adherent material in the cortex for its lesion risk; placement of subdural drainage can be left up to 72h. In our case, the realization of minicraniotomy does not allow an extensive cavity wash, and the initial treatment with cefotaxime (2g/8h) was with low dose; these may favor the recurrence.

In conclusion, the spontaneous SE should be suspected in patients with fever and hypodense subdural collections in the head CT, and the administration of intravenous contrast may to increase its sensitivity. To achieve a favorable outcome must make an early surgery and begin antibiotic therapy. It seems that the craniotomy is associated with a lower relapse rate, however more studies are needed to confirm this fact.

References
[1]
S. Bakker, J. Kluytmans, J.C. den Hollander, S.T. Lie.
Subdural empyema caused by Escherichia coli: hematogenous dissemination to a preexisting chronic subdural hematoma.
Clin Infect Dis, 21 (1995), pp. 458-459
[2]
C.J. Miedema, J.L. Kimpen.
Hematogenous dissemination of Escherichia coli to a preexistent subdural hematoma in a child.
Clin Infect Dis, 23 (1996), pp. 662
[3]
N. Yilmaz, N. Kiymaz, C. Yilmaz, A. Bay, S.A. Yuca, C. Mumcu, et al.
Surgical treatment outcome of subdural empyema: a clinical study.
Pediatr Neurosurg, 42 (2006), pp. 293-298
[4]
K.S. Yoon, G.T. Yee, S.R. Han, C.H. Lee.
Escherichia coli subdural empyema following subdural hygroma in elderly patient.
J Korean Neurosurg Soc, 47 (2010), pp. 470-472
[5]
R. Redhu, A. Shah, M. Jadhav, A. Goel.
Spontaneous tension pneumocephalus in a patient with subdural empyema.
J Clin Neurosci, 18 (2011), pp. 1123-1124
[6]
M. Kaminogo, M. Kurihara, T. Kawano, K. Mori, M. Yasuda.
A case of infected subdural hematoma (subdural empyema) secondary to septicemia caused by agranulocytosis.
No Shinkei Geka, 12 (1984), pp. 353-357
[7]
A.A. Adamides, T. Goldschlager, S.J. Tulloch, J.H. McMahon.
Pneumocephalus from gas-forming Escherichia coli subdural empyema.
Br J Neurosurg, 21 (2007), pp. 299-300
[8]
H. Nishi, Y. Shibagaki, S. Hatakeyama, T. Ito, T. Nagata, M. Ohno, et al.
Metastatic intracranial subdural empyema from renal cyst infection in autosomal dominant polycystic kidney disease.
Nephrol Dial Transplant, 20 (2005), pp. 2820-2823
[9]
C. Bachmeyer, M. Logak, W. Ammouri, A.S. Blanc.
Spontaneous Escherichia coli meningitis with subdural empyema in an adult.
South Med J, 98 (2005), pp. 1225-1226
[10]
L.J. Fender, R.K. Lenthall, T. Jaspan.
De novo development of presumed cavernomas following resolution of E. coli subdural empyemas.
Neuroradiology, 42 (2000), pp. 778-780
Copyright © 2015. Elsevier España, S.L.U. and Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica
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