Isolated Myelitis and Intramedullary Spinal Cord Abscess in Melioidosis—A Case Report

2021 ◽  
pp. 194187442110253
Author(s):  
Pavankumar Rudrabhatla ◽  
Sruthi S. Nair ◽  
Jithin George ◽  
Sabarish Sekar ◽  
Dinoop Korol Ponnambath

Neuromelioidosis is a severe tropical infection with high morbidity and mortality. Isolated myelitis is an extremely rare manifestation of melioidosis which may evade diagnosis. We report a 69-year-old diabetic male patient who presented with acute flaccid paraplegia and longitudinally extensive myelitis and no systemic symptoms. MRI of spinal cord showed lower dorsal cord and conus T2 hyperintensity and microabscesses with dural enhancement. The diagnosis was clinched with blood culture growing Burkholderia pseudomallei. He rapidly developed colitis, septicemia and multiorgan dysfunction and succumbed to the illness in spite of antibiotics and aggressive supportive care. The case highlights that melioidosis should be considered as a differential diagnosis of infectious myelitis, especially in the tropics. Presence of a neutrophilic blood and cerebrospinal fluid picture and microabscesses in spinal cord are important diagnostic clues. The outcome is dismal unless the diagnosis is considered early in the disease course and managed expeditiously with sensitive antibiotics.

Neurosurgery ◽  
1990 ◽  
Vol 26 (1) ◽  
pp. 145-146 ◽  
Author(s):  
Barbara S. Koppel ◽  
Michael Daras ◽  
Kent R. Duffy

Abstract Viral myelitis and bacterial epidural infections are common in intravenous drug abusers, but primary infections of the spinal cord are extremely rare. We report a 50-year-old active intravenous drug user who developed tetraplegia from an intramedullary abscess caused by Pseudomonas cepacia. Despite neurosurgical drainage and appropriate antibiotic therapy, no improvement was seen. Earlier intervention and a high index of suspicion is required in patients with a history of intravenous drug abuse and spinal cord symptoms. (Neurosurgery 26:145-146, 1990)


2020 ◽  
Vol 82 ◽  
pp. 249-251
Author(s):  
Takayoshi Akimoto ◽  
Satoshi Hirose ◽  
Tomotaka Mizoguchi ◽  
Yuki Yokota ◽  
Makoto Hara ◽  
...  

2009 ◽  
Vol 49 (6) ◽  
pp. 262-268 ◽  
Author(s):  
Noriaki KURITA ◽  
Yasuhisa SAKURAI ◽  
Makoto TANIGUCHI ◽  
Toru TERAO ◽  
Hiroshi TAKAHASHI ◽  
...  

2009 ◽  
Vol 4 (3) ◽  
pp. 254-261 ◽  
Author(s):  
Katrin Scheinemann ◽  
Ute Bartels ◽  
Annie Huang ◽  
Cynthia Hawkins ◽  
Abhaya V. Kulkarni ◽  
...  

Object Intramedullary spinal cord low-grade gliomas (LGGs) are rare CNS neoplasms in pediatric patients, and there is little information on therapy for and outcome of these tumors in this population. Furthermore, most patient series combine adult and pediatric patients or high- and low-grade tumors, resulting in controversial data regarding optimal treatment of these children. To clarify these issues, the authors performed a regional population-based study of spinal cord LGGs in pediatric patients. Methods All pediatric patients with LGGs treated during the MR imaging era (1985–2007) were identified in the comprehensive database of the Hospital for Sick Children in Toronto. Data on demographics, pathology, treatment details, and outcomes were collected. Results Spinal cord LGGs in pediatric patients constituted 29 (4.6%) of 635 LGGs. Epidemiological and clinical data in this cohort were different than in patients with other spinal tumors and strikingly similar to data from pediatric patients with intracranial LGGs. The authors observed an age peak at 2 years and a male predominance in patients with these tumors. Histological testing revealed a Grade I astrocytoma in 86% of tumors. Although 5-year progression-free survival for the entire group was 48 ± 9%, all patients were alive at a median follow-up of 8.2 years. Five-year progression-free survival was 88 ± 13% for patients undergoing gross-total resection and 34 ± 11% for those undergoing all other therapies, respectively (p = 0.02). Chemotherapy and radiation therapy showed similar efficacy, achieving sustained tumor control in most patients. However, this excellent survival rate was associated with an 83% rate of significant neurological and orthopedic sequelae. Conclusions This study provides basic data on the incidence, clinical course, and outcome of spinal cord LGGs in pediatric patients. The similarities between spinal and intracranial LGGs in pediatric patients showing excellent survival but high morbidity suggest that a less aggressive approach may be the preferable treatment option for these patients.


2011 ◽  
Vol 2011 (may08 1) ◽  
pp. bcr1120103512-bcr1120103512 ◽  
Author(s):  
K. Higuchi ◽  
H. Ishihara ◽  
S. Okuda ◽  
F. Kanda

1992 ◽  
Vol 55 (3) ◽  
pp. 225-226 ◽  
Author(s):  
M E M. Carus ◽  
B Anciones ◽  
A Castro ◽  
M Lara ◽  
A Isla

1992 ◽  
Vol 38 (4) ◽  
pp. 287-290 ◽  
Author(s):  
Jonathan H. Erlich ◽  
Jeffery V. Rosenfeld ◽  
Andrew Fuller ◽  
Graham V. Brown ◽  
Jack Wodak ◽  
...  

2015 ◽  
Vol 06 (04) ◽  
pp. 261-263
Author(s):  
T.P. Yadav ◽  
Vivek Dewan ◽  
Divya Jain ◽  
Sandeep Choudhary

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