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Table 2 Differential diagnosis of Hashimoto’s encephalopathy (along with relevant clinical features and lab investigation)

From: Streaming through a case of SREAT

Sl no.

Category

Disease

Differentiating clinical features (signs and symptoms)

Relevant laboratory investigation

1

Infective

Meningitis

Fever, neck stiffness, positive Kernig’s and Brudzinski sign

CSF showing increased WBCs with neutrophilic or lymphocytic predominance; variable protein and glucose levels depending on the micro-organism involved

Encephalitis

Seizure episode and focal neurologic findings are characteristic; other features may be common

Neuroimaging is required to localise any specific area of inflammation or lesion

2

Vascular

Cerebral vasculitis

Widespread systemic involvement along with CNS involvement. Present with skin rash, joint pains or fatigue

Cerebral angiography showing inflamed vessels

Cerebrovascular accidents (CVA)/ transient ischaemic ATTACK

Focal neurologic finding, unilateral or bilateral limb weakness sings of lobar involvement or cranial nerve palsy, bulbar signs, Babinski sign positive

CT scan/MRI showing haemorrhagic or ischaemic lesion in the cerebral area or brainstem

3

Neoplastic

Tumours of the brain or spinal cord/Metastasis to the brain

Present with focal symptoms, weight loss, anorexia, early morning headache or signs of increased intracranial pressure. Mass effects

Neuroimaging is required to localise the lesion. PET scan to diagnose any metastasis. Other relevant imaging to find the source

4

Traumatic

Any road traffic accident involving Brain/spinal cord

Variable depending on area of lesion. Obvious signs and history of injury. Cushing's triad may be present. Basilar skull fracture, ecchymosis of eyes and CSF leak

Comprehensive imaging and screening,

5

Metabolic

Toxin induced (can be from substance abuse, prescription drugs or poison)

Variable symptoms depending on the nature of substance

Clinical; urine drug screening

Hepatic or Uremic Encephalopathy

Asterixis, focal seizures, low urine output, altered sleep wake cycle

Clinical, urea and ammonia levels,

Hypertensive encephalopathy

Variable symptoms (gait disturbance; headache; vomiting)

Serial BP measurements, electroencephalogram (EEG), ECG

Nutritional Encephalopathy (glycopenic, Wernicke’s)

Drowsiness, autonomic hyperactivity, sweating, confusion, ataxia, nystagmus

Blood glucose levels or vitamin B1 levels. In neuroglycopenia MRI brain may show T2 hyper intensity in basal ganglia, thalamus, cortex and splenium involvement may show ‘boomerang sign’

6

Autoimmune

Anti-NMDAR Encephalopathy

Flu-like illness, along with encephalopathic symptoms and then progression to psychosis, paranoia or agitation

anti-NMDAR antibody + in CSF and/or serum, EEG

Paraneoplastic limbic encephalitis

Associated with an underlying malignancy of lung or breast, amnesia, complex seizures and temporal lobe involvement

Anti-Hu+, anti-Ma+ in CSF and/or serum, EEG showing epileptic activity

Paraneoplastic cerebellar degeneration

Associated with an underlying malignancy of lung, ovary or breast; bulbar palsy along with vertigo or tremor

Anti-Yo, anti-Hu, anti-Ri antibodies in csf and/or serum

Hashimoto's encephalopathy

Altered sensorium, stroke-like episode, myoclonus, seizures, vertigo, headache

Anti-TPO antibodies in CSF and/or serum, MRI enhancement in basilar regions

7

Degenerative

Creutzfeldt–Jakob disease

Behavioural change, psychosis, dementia, involuntary movements and coma

EEG showing periodic sharp wave pattern, CSF having 14–3–3 protein