scholarly journals Unravelling diagnostic dilemma: AQP4-Positive transverse myelitis mimics spinal intramedullary tumor

2021 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
M Netravathi ◽  
NeeharikaSriram Ramalakshmi ◽  
Dwarakanath Srinivas ◽  
Anita Mahadevan
2019 ◽  
Vol 10 (04) ◽  
pp. 703-706
Author(s):  
Ravi K. Anadure ◽  
Jitesh Goel ◽  
S. Sahu ◽  
Tushar Vidhale

AbstractBrucellosis (malta fever) is a zoonotic infection caused by a gram-negative coccobacillus which is a facultative intracellular pathogen. It causes a chronic granulomatous infection, similar in histology to tuberculosis. Brucellosis remains a diagnostic dilemma due to misleading, nonspecific manifestations and increasing trend of unusual presentations. In brucellosis, the nervous system involvement occurs in only 5 to 7% of untreated patients, and it may manifest with encephalitis, meningoencephalitis, radiculitis, and peripheral and cranial neuropathies. Transverse myelitis is an unusual occurrence. Here, the authors are reporting an unusual case of neurobrucellosis in an elderly male patient who visited multiple hospitals with recurring febrile encephalopathy and paraparesis. The diagnosis was suspected by his occupational history of working as an abattoir worker and was confirmed by the presence of high titers of Brucella immunoglobulin (Ig) M and IgG antibodies in the serum. The patient was managed with injection gentamicin for 2 weeks along with oral course of doxycycline and rifampicin for 6 weeks. He made a good clinical recovery and went back to work with mild residual deficits.


2019 ◽  
Vol 10 (04) ◽  
pp. 693-696
Author(s):  
Rajesh Verma ◽  
Chetan Kumar

AbstractTumefactive demyelination is an uncommon neurological disorder mimicking tumors. It is one of the rare varieties of demyelinating disorders, often causing diagnostic dilemma among neuroscientists. The literature tells us about approaching these patients added by peculiar neuroimaging findings. Neuromyelitis optica is an immune mediated inflammatory clinical disorder, typically involving optic nerves bilaterally and longitudinally extensive transverse myelitis. With the revelation of aquaporin four channels, its distribution in the brain and related antibody, the concept of neuromyelitis optica spectra disorders has been evolved. In this case report, our intention is to present a young female who presented with bilateral vision loss with tumor-like mass lesion in cerebral cortex. Such an association of bilateral optic neuropathy involving chiasmatic region, suggestive of neuromyelitis optica spectrum disorder (NMOSD) with tumefactive demyelination is rarely reported in the literature.


2019 ◽  
Vol 25 ◽  
pp. 143-144
Author(s):  
Muhammad Ansar ◽  
Joseph Dillon
Keyword(s):  

2016 ◽  
Vol 47 (S 01) ◽  
Author(s):  
V. Kraus ◽  
C. Makowski ◽  
H. Jünger ◽  
A. Wawer ◽  
P. Strotmann ◽  
...  

2016 ◽  
Vol 36 (03) ◽  
pp. 180-182
Author(s):  
F. Dressler ◽  
H. Hartmann ◽  
E. Bültmann ◽  
N. Schwerk ◽  
A. Thon ◽  
...  

Author(s):  
Deirdre O'Sullivan ◽  
Michael Moore ◽  
Susan Byrne ◽  
Andreas O. Reiff ◽  
Susanna Felsenstein

AbstractAcute disseminated encephalomyelitis in association with extensive longitudinal transverse myelitis is reported in a young child with positive anti-myelin oligodendrocyte glycoprotein (MOG) antibody with heterozygous NLRP3 missense mutations; p.(Arg488Lys) and p.(Ser159Ile). This case may well present an exceptional coincidence, but may describe a yet unrecognized feature of the spectrum of childhood onset cryopyrinopathies that contribute to the understanding of the genetic basis for anti-MOG antibody positive encephalomyelitis. Based on this observation, a larger scale study investigating the role of NLRP3 and other inflammasomes in this entity would provide important pathophysiological insights and potentially novel avenues for treatment.


2005 ◽  
Vol 209 (S 1) ◽  
Author(s):  
K Petersen ◽  
T Rettig ◽  
A Lingenauber ◽  
D Weise ◽  
A von der Wense
Keyword(s):  

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