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Inicio Neurología (English Edition) Cerebral abscess due to Rhodococcus equi with pseudotumour presentation in an im...
Información de la revista
Vol. 28. Núm. 8.
Páginas 522-524 (octubre 2013)
Vol. 28. Núm. 8.
Páginas 522-524 (octubre 2013)
Letter to the Editor
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Cerebral abscess due to Rhodococcus equi with pseudotumour presentation in an immunocompetent patient
Absceso cerebral por Rhodococcus equi con comportamiento seudotumoral en paciente inmunocompetente
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A. Velázquez Benito
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albavelazquez83@gmail.com

Corresponding author.
, C. Tejero Juste, C. Pérez Lázaro, S. Santos Lasaosa
Servicio de Neurología, Hospital Clínico Lozano Blesa, Zaragoza, Spain
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Dear Editor,

Infections by Rhodococcus species are very rarely seen in humans.1,2 We present the case of a 52-year-old Spanish-born male construction worker with a history of hypertension and moderate heart failure and no history of habitual contact with animals. Over a period of 2 weeks, the patient had experienced progressive symptoms of disorientation in time and space, mobility limitations, and language difficulties. He was transported to our hospital's emergency department for those reasons. Physical examination upon admission revealed disorientation in time and space, frank bradypsychia, mild right brachial paresis, motor aphasia, apathy, and aboulia. The general examination, including cardiopulmonary auscultation, yielded normal results. Vital signs recorded by the emergency department were also normal (blood pressure, heart rate, temperature, and oxygen saturation). Emergency laboratory analyses and chest radiography showed no abnormalities. An emergency CT study (Fig. 1) revealed a left frontal–temporal mass 45mm in diameter. The mass was cavitated, with a small haemorrhagic area and perilesional oedema. Since doctors suspected a malignant tumour, they began corticosteroid treatment with dexamethasone dosed at 8mg every 8h, intravenous analgesics, and low molecular-weight heparin at a prophylactic dose. The blood test performed as part of the study delivered the following results. Complete blood count (haemoglobin 16g/dL, WBC count 9000/mm3, neutrophils 70%, platelets 282000/mm3); coagulation study (normal); cellular immunity study (CD4 lymphocytes 45%, CD8 lymphocytes 24%, CD4–CD8 ratio 1.9); immunoglobulins test (normal); negative for HIV. The magnetic resonance study (Fig. 2) using normal sequences (T1, T2, and proton-density weighted) revealed a lesion that was hypointense in T1 and hyperintense in T2. It was located in the left frontal-temporal area and surrounded by an extensive hyperintense perilesional halo with collapsed sulci and slight subfalcine herniation. Contrast uptake was ring-shaped; this pattern, together with clinical data, was compatible with highly malignant glioma. Diffusion sequence and spectroscopy results are not available since we did not have access to those techniques.

Figure 1.

Brain CT without contrast showing a space-occupying lesion in the left frontal–temporal area with significant perilesional oedema and a midline shift.

(0.14MB).
Figure 2.

Brain MRI, T2-weighted sequence.

(0.09MB).

Focal motor signs and bradypsychia improved partially in the first few days of hospitalisation. One week later, the patient experienced sudden-onset chest pain, associated dyspnoea, and low oxygen saturation. Based on a suspected diagnosis of pulmonary embolism, we performed an emergency thoracic CT study that revealed multiple bilateral pulmonary nodules that were cavitated. These data, plus the patient's medical history and the previous laboratory analyses and imaging studies, suggested a secondary disease. The patient required orotracheal intubation and was moved to the intensive care unit. In the following days, his condition deteriorated rapidly and he developed a fever. Doctors took blood and urine cultures, bronchoalveolar lavage (BAL) sample, and a tracheal aspirate culture. The brain lesion was biopsied and the analysis revealed cystic tissue containing unrecognisable cellular material. The microbial study identified Rhodococcus equi. The BAL sample also tested positive for Nocardia and Aspergillus. Likewise, the tracheal aspirate culture showed nocardiform bacteria and the blood culture confirmed the presence of Rhodococcus equi. Intravenous antibiotic treatment with amikacin and meropenem elicited no improvement. Later neuroimaging studies showed no changes and the following chest CT confirmed the presence of necrotising invasive aspergillosis. The patient died several days later with a final diagnosis of adult respiratory distress caused by a mixed infection (Aspergillus/Rhodococcus/Nocardia) and cerebral abscess caused by Rhodococcus equi.

Brain abscesses are suppurative processes of the cerebral parenchyma with high morbidity and mortality rates.3 They are slightly more prevalent in men and most often occur during the 6th and 7th decades of life. A compromised immune system and ENT surgery or neurosurgery are known risk factors for these abscesses. The causal agents may be aerobic or anaerobic, although studies are most likely to identify mixed polymicrobial flora. In cases of weakened immune system, the microbes may be uncommon (opportunistic micro-organisms). Rhodococcus equi is one such micro-organism.4,5 This environmental zoonotic pathogen belongs to the Nocardiaceae (along with the Nocardia and Gordona genera, a fact which explains the presence of the multiple types of micro-organisms in the patient's respiratory system samples). The most common infection route is respiratory contamination after contact with carrier animals. The prevalence of infection with this microbe is low, but it has risen as the HIV infection rate has increased. The most reliable diagnostic tests are sputum sample and blood culture. In humans, Rhodococcus equi6,7 produces cavitated lesions containing abundant intracellular bacteria. Its main manifestation is insidious respiratory infection; less frequently, it may infect other organs, including the brain, liver, kidneys, or eyes (endophthalmitis). There is no consensus regarding what treatment should be used, or the treatment duration. The most common recommendation5,8 is to administer erythromycin with vancomycin or rifampicin during at least 3 weeks. The literature describes only a few cases, but infection with Rhodococcus equi may also present in immunocompetent patients, as in our case. Early diagnosis and effective treatment are therefore crucial to minimise the complications of this disease.

References
[1]
S. Uliversi, G. Oliveri.
Cerebellar abscess due to Rhodococcus equi in an inmunocompetente patient: case report and literature review.
J Neurosurg Sci, 50 (2006), pp. 127-129
[2]
N. Sánchez, A. Sandoval, F. Díaz, J. Serrano.
El género Rhodococcus: una revisión didáctica.
Rev Soc Ve Microbiol, 24 (2004),
[3]
M. Gutiérrez, M.A. Ballesteros, A. Vallejo, E. Miñambres, C. Fariñas-Álvarez, J.D. García.
Abscesos cerebrales en un hospital de tercer nivel: epidemiología y factores que influyen en la mortalidad.
Rev Esp Quimioter, 22 (2009), pp. 201-206
[4]
T.D. Verville, M.M. Huycke, R.A. Greenfield, D.P. Fine, T.L. Kuhis, L.N. Slater.
Rhodococcus equi infections of humans: 12 cases and review of the literature.
Medicine (Baltimore), 73 (1994), pp. 119-132
[5]
P. Gabriels, H. Joosen, E. Put, J. Verhaegen, K. Magerman, R. Cartuyvels.
Recurrent Rhodococcus equi infection with fatal outcome in an immunocompetent patient.
Eur J Clin Microbiol Infect Dis, 25 (2006), pp. 46-48
[6]
M. Kamboj, A. Kalra, V. Kak.
Rhodococcus equi brain abscess in a patient without HIV.
J Clin Pathol, 58 (2005), pp. 423-425
[7]
X.-Y. Chen, F. Xu, J.-Y. Xia, Y.-S. Cheng, Y. Yang.
Bacteriemia due to Rhodococcus equi: a case report and review of the literature.
J Zhejiang Univ Sci, 10 (2009), pp. 933-936
[8]
W.G. Obana, K.A. Scannell, R. Jacobs, C. Greco, M.I. Rosenblum.
A case of Rhodococcus equi brain abscess.
Surg Neurol, 35 (1991), pp. 321-324

Please cite this article as: Velázquez Benito A, Tejero Juste C, Pérez Lázaro C, Santos Lasaosa S. Absceso cerebral por Rhodococcus equi con comportamiento seudotumoral en paciente inmunocompetente. Neurología. 2013;37:522–524.

Copyright © 2011. Sociedad Española de Neurología
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