Severe form of radiculo - myelo - neuropathy with meningo - encephalitis secondary to Angiostrongylus cantonensis infection: Unusual corpus callosal lesions and serial magnetic resonance imaging findings

2013 ◽  
Vol 61 (4) ◽  
pp. 414 ◽  
Author(s):  
Atchayaram Nalini ◽  
Anil Ramakrishna ◽  
Paron Dekumoy ◽  
RajuRavi Kumar ◽  
Wallop Pakdee ◽  
...  
2005 ◽  
Vol 91 (5) ◽  
pp. 1237-1239 ◽  
Author(s):  
Lian-Chen Wang ◽  
Dinah-Pingni Wan ◽  
Shih-Ming Jung ◽  
Chien-Chuan Chen ◽  
Ho-Fai Wong ◽  
...  

1997 ◽  
Vol 37 (12) ◽  
pp. 924-928 ◽  
Author(s):  
Satoshi NAKASU ◽  
Takahiro ISOZUMI ◽  
Atsushi YAMAMOTO ◽  
Kiyoharu OKADA ◽  
Tomoyuki TAKANO ◽  
...  

2018 ◽  
Author(s):  
Jong Hyuk Kim ◽  
Noh Hyuck Park

Abstract Background: The authors report serial magnetic resonance imaging findings of osmotic demyelination syndrome (ODS) related to hyperglycemia in a patient with uncontrolled diabetes mellitus. Case presentation: A 61-year-old man with diabetes was admitted for general weakness and severe thirst. A few days later, he complained of dysarthria, dysphasia, and dysmetria. On admission, he exhibited significant hyperglycemia (33.5 mmol/L [627 mg/dL]), with a glycated hemoglobin level of 18.1%. Other laboratory investigations revealed a sodium level of 133 mEq/L, potassium 3.8 mEq/L, blood urea nitrogen 43.9 mg/dL, with a calculated serum osmolality of 324 mOsm/kg. Brain magnetic resonance imaging (MRI) revealed T2 signal abnormalities that were symmetrical, non-space occupying, and located in the central pons with a peripheral sparing pattern, which were findings suggestive of ODS. In addition, subsequent MRI revealed progression of signal hyperintensity; however, the patient's symptoms were improved and he was discharged after 2 months. Conclusion: We report a rare case of hyperglycemia-related ODS that exhibited gradual progression in imaging features despite the prompt correction of blood sugar levels and improvement of neurological symptoms


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