Showing posts with label hemiatrophy dds. Show all posts
Showing posts with label hemiatrophy dds. Show all posts

Friday, 7 October 2011

All hemiatrophies are not Rasmussen's

A 14yo female with seizures, poor school performance.
Present MRI study shows moderate left hemi atrophy.
Previous CT study of Brain done 5 year back noted and is normal. 
The striking feature of this MRI study is left hemi atrophy.
Imaging wise Rassmussen’s Encephalitis was suggested at first. But.........!!!

Detailed history and history of previous hospital admission reviewed again which revealed, her previous hospital admission for fever and loss of consciousness 5 year back.
The CT which was at that time was normal.
MRI not done.
Csf findings and discharge summery mentions clinical diagnosis of Encephalitis.
After that till now hardly had 2 or three episodes of seizures. Is under treatment of anti epileptics and responding well to medication. There is no clinical worsening or progression in seizures so far. 

In Rasmussen’s, hemi atrophy is rapidly progressive, an associated progressive clinical worsening, intractable seizures which are non responsive to medications.  

DDs:
Now as per the clinical details and imaging finding left Hemi atrophy as a sequel of previous Encephalitis is more likely than Rasmussen’s among the two.
Peri natal hemispheric infarction (Dyke Davidoff Masson syndrome) is unlikely as there is no history of significant perinal insult, no associated compensatory ipsilateral bony calvarial thickening, hyper pneumatisation of paranasal sinuses, elevation of petrous ridge.  

Conclusion : All hemiatrophies are not Rasmussen’s. Clinical course is equally important. Better to give DDs. 

Friday, 9 September 2011

Rasmussen Encephalitis MRI


Imaging wise characterized by hemi atrophy as in this case on right side.
Atrophy is progressive, may be associated with cortical gliosis.

Rasmussen Encephalitis, a chronic progressive encephalitis results in severe, intractable epilepsy.
Seizures typically are focal motor type, begin abruptly in previously normal children. Follows by motor function deterioration with hemi paresis or hemiplegia, progressive cognitive decline
Etiology unknown.
Proposed hypothesis is autoimmunity associated with persistent viral infection.
Refractory to medical treatment.
Surgical treatment is functional hemispherectomy.

Imaging wise DDs:
1. Peri natal hemispheric infarction (Dyke Davidoff Masson syndrome) 
characterized by hemi atrophy with an associated compensatory ipsilateral bony calvarial thickening, hyper pneumatisation of paranasal sinuses, elevation of petrous ridge.  
2. Sequel of previous Encephalitis 
in which case atrophy is non progressive, pt clinically will not show worsening , respond well to medications, history of previous hospitalization for encephalitis if any.