Infect Chemother. 2008 Jul-Aug;40(4):230-232. English.
Published online Aug 31, 2008.
Copyright © 2008 The Korean Society of Infectious Diseases and The Korean Society for Chemotherapy
Case Report

A Case of Cervical Epidural Abscess Presenting Rapidly Progressing Quadriplegia without any other Symptom or Sign of CEA

Hyun-Jeung Yu, M.D.,1 Sook Young Roh, M.D.,1 and Seong-Ho Koh, M.D.2
    • 1Department of Neurology, Bundang Jesaeng General Hospital, Korea.
    • 2Department of Neurology, College of medicine, Haynang University, Korea.
Received March 28, 2007; Accepted September 18, 2007.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Cervical epidural abscess (CEA) is a very uncommon disease with diverse clinical presentations. Clinically, it is difficult to diagnose this disease, especially in early stage. We report an atypical case of CEA showing only progressive quadriparesis without any other symptoms or signs of CEA. From this experience, CEA must be considered when progressive quadriparesis without any specific cause is developed in immuno-compromised patients and diabetic patients with polyneuropathies.

Keywords
Cervical epidural abscess; Quadriparesis; Diabetes Mellitus

Introduction

Cervical epidural abscess (CEA) is an uncommon disease with diverse clinical presentations. Clinically, it is difficult to diagnose this disease, especially in early stage (1). Early diagnosis of CEA became more frequent with recent development of diagnostic radiology (2). Considering that CEA can cause permanent neurologic deficits if early surgical treatment is not performed (3), the importance of early diagnosis of CEA can not be emphasized enough. Therefore, if a patient shows fever, back pain, and progressive neurologic deficits such as quadriparesis, sphincter dysfunction, and a detectable sensory level, we must consider CEA as the underlying disease (1, 4). We report an atypical case of CEA showing only progressive quadriparesis without any other symptoms or signs of CEA.

Case report

A 71-year-old male with chronic renal failure and diabetes mellitus was admitted for hemodialysis. On admission, vital signs were stable except for mild fever, up to 37.8℃. Mild leukocytosis (11,500/mm3), was revealed in a complete blood count, and an increased blood urine nitrogen (92.7 mg/dL), creatinine (4.7 mg/dL) and serum glucose level (306 mg/dL) were confirmed in blood chemistry. Two hours after the admission, the patients body temperature had increased to 38.3℃ and chest x-ray, blood culture and urine culture were also performed to find the focus of the fever. Also, empirical antibiotics were started. On the second day of admission, body temperature was normalized to 36.5℃ and leukocyte levels decreased to 8,300/mm3. Antibiotics were discontinued and hemodialysis was performed. On the fifth day of admission, progressive quadriparesis beginning from both legs were detectes and a neurologist was consulted for evaluation. At that time, vital signs were stable (120/80-36.8℃-20), while physical examinations showed generalized edema and an appearance indicating chronic illness. A neurologic examination revealed Medical Research Council (MRC) grade IV deficit in the upper extremities and grade III in lower extremities. Also, position and vibration senses were abolished in all extremities, and deep tendon reflexes were decreased in all extremities. Pain and temperature senses were relatively intact and no other neurologic abnormalities, including neck stiffness and sphincter dysfunction, were found. To rule out rapidly progressing acute inflammatory demyelinating polyneuropathy, electromyographic (EMG), nerve conduction (NCS) and cerebrospinal fluid (CSF) studies were performed. The EMG and NCS tests revealed sensory-motor polyneuropathy. The CSF study revealed a leukocyte count of 425/µL (polymorphonuclear leukocyte - 73%), a red blood cell count of 6/µl, a glucose level of 50 mg/dL (serum glucose level was 288 mg/dL), and a protein level of 1168.8 mg/dL. On the sixth day, his motor symptoms grew worsened to grade I in upper extremities and grade 0 in lower extremities. Emergency spinal magnetic resonance imaging was performed, which confirmed a cervical epidural abscess between the fourth and fifth cervical vertebrae (Fig. 1). After emergency surgery, he was treated with broad spectrum antibiotics. Despite the emergency surgery, his motor symptoms did not improve. Blood and abscess cultures showed Methicillin-resistant Staphylococcus aureus. The patient expired despite the treatment with broad spectrum antibiotics for more than a month.

Figure 1
T2-wieghted midline saggital image of the patient revealed a C1-C4 compressive myelopathy caused by infectious spondylitis, prevertebral and anterior epidural abscess at the C4 and C5 vertebral bodies.

Discussion

Cervical epidural abscess (CEA) is a very uncommon neurological infectious disease requiring emergency treatment. According to Lasker et al., the incidence of CEA varies between 1 in 70,000 and 1 in 400,000 admissions at major academic teaching hospitals in USA(3). About 70% of spinal epidural abscesses occur between age 31 and 70, with no tendency to any particular decade (5). Staphylococcus is the most common causative organism and accounts for 63% of the cultured organisms (1). The most common risk factor is known to be diabetes mellitus, followed by trauma, intravenous drug abuse, and alcoholism (5). Fever, back pain and progressive neurologic deficits are considered to be the triad of spinal epidural abscess (1, 4, 6) but CEA presenting all these typical symptoms is very rare, and the disease is especially difficult to diagnose in early stages because of the diversity of its clinical course (1). Although earlier diagnoses have been recently achieved with the development of sophisticated imaging. However, it is still difficult to diagnose CEA, especially when it shows an atypical clinical presentation as it did in the early days of this case.

Park et al. reported a case of CEA in 1993 which presented with complete loss of sensory sunctions including pain, temperature, position and vibration, below the fourth thoracic level and progressive paralytic motor weakness (7), but only transient and mild fever and progressive motor weakness were observed in this case. In immuno-compromised patients, as in this case, fever may not appear in spite of CEA (1, 4, 6, 7). Also, it is possible that peripheral polyneuropathies caused by underlying diabetes mellitus may have might masked any specific sensory abnormalities induced by CEA.

References

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    1. Kricun R, Shoemaker EI, Chovanes GI, Stephens HW. Epidural abscess of the cervical spine: MR findings in five cases. AJR Am J Roentgenol 1992;158:1145–1149.
    1. Lasker BR, Harter DH. Cervical epidural abscess. Neurology 1987;37:1747–1753.
    1. Hancock DO. A study of 49 patients with acute spinal extradural abscess. Paraplegia 1973;10:285–288.
    1. Reihsaus E, Waldbaur H, Seeling W. Spinal epidural abscess: a meta-analysis of 915 patients. Neurosurg Rev 2000;23:175–204.
    1. Pereira CE, Lynch JC. Spinal epidural abscess: an analysis of 24 cases. Surg Neurol 2005;63 Suppl 1:S26–S29.
    1. Park HM, Kim SH, Kim J, Kim MH. Epidural abscess secondary to acute osteomyelitis of the cervical spine caused by E. coli. J Korean Neurol Assoc 1993;11:630–633.

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