Human Parechovirus Encephalitis As an Important Differential Diagnosis of White Matter Lesions in Neonatal Sepsis-Like Illness

2014 ◽  
Vol 45 (S 01) ◽  
Author(s):  
L. Freudenberg ◽  
S. Brenner ◽  
G. Hahn ◽  
M. van der Knaap ◽  
M. Smitka ◽  
...  
1998 ◽  
Vol 5 (10) ◽  
pp. 737-738
Author(s):  
Toni C. Roth ◽  
Beverly L. Hershey ◽  
Amy L. Kotsenas ◽  
Todd L. Siegal

2014 ◽  
Vol 24 (2) ◽  
pp. 93-110 ◽  
Author(s):  
S. Weidauer ◽  
M. Nichtweiß ◽  
E. Hattingen

2019 ◽  
Vol 62 (3) ◽  
pp. 123-126
Author(s):  
Iveta Chroustová ◽  
Miroslav Mareš ◽  
Leoš Ungermann ◽  
Edvard Ehler

Antibodies against myelin oligodendrocyte glycoprotein cause inflammatory lesions of central myelin – in optic nerves, of the brainstem, and spinal cord. There are characteristic changes of CNS white matter, protein-cytological association in cerebrospinal fluid, MOG IgG antibodies, a very important differential diagnosis and a relatively mild course.


1999 ◽  
Vol 19 (5) ◽  
pp. 330-336 ◽  
Author(s):  
W Thomas Bass ◽  
Martha A Jones ◽  
Larry E White ◽  
Thomas R Montgomery ◽  
Frank Aiello ◽  
...  

2017 ◽  
Vol 15 ◽  
pp. 42-46 ◽  
Author(s):  
Mariano Marrodan ◽  
Jorge Correale ◽  
Lucas Alessandro ◽  
Mariela Amaya ◽  
Maria Eugenia Fracaro ◽  
...  

Sensors ◽  
2021 ◽  
Vol 21 (21) ◽  
pp. 7127
Author(s):  
Małgorzata Siger ◽  
Marta Owidzka ◽  
Mariola Świderek-Matysiak ◽  
Wojciech Omulecki ◽  
Mariusz Stasiołek

In the differential diagnosis of nonspecific white matter lesions (NSWMLs) detected on magnetic resonance imaging (MRI), multiple sclerosis (MS) should be taken into consideration. Optical coherence tomography (OCT) is a promising tool applied in the differential diagnostic process of MS. We tested whether OCT may be useful in distinguishing between MS and NSWMLs patients. In patients with MS (n = 41) and NSWMLs (n = 19), the following OCT parameters were measured: thickness of the peripapillary Retinal Nerve Fibre Layer (pRNFL) in superior, inferior, nasal, and temporal segments; thickness of the ganglion cell-inner plexiform layer (GCIPL); thickness of macular RNFL (mRNFL); and macular volume (MV). In MS patients, GCIPL was significantly lower than in NSWMLs patients (p = 0.024). Additionally, in MS patients, mRNFL was significantly lower than in NSWMLs patients (p = 0.030). The average segmental pRNFL and MV did not differ between MS and NSWMLs patients (p > 0.05). GCIPL and macular RNFL thinning significantly influenced the risk of MS (18.6% [95% CI 2.7%, 25.3%]; 27.4% [95% CI 4.5%, 62.3%]), and reduced GCIPL thickness appeared to be the best predictor of MS. We conclude that OCT may be helpful in the differential diagnosis of MS and NSWMLs patients in real-world settings.


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