Evidence map›Paper›PMID 41113073›Full record

ArticleWorld journal of clinical cases2025

Silent triggers and symmetric peduncles - a rare presentation of adult-onset acute disseminated encephalomyelitis: A case report.

Affan Faisal, Zain Tariq, Rania Usman Latif, Saim Amir, Abdul Basit, Abdul M Basil

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Article in World journal of clinical cases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Affan FaisalDepartment of Medicine, King Edward Medical University, Lahore 54000, Punjab, Pakistan.
Zain TariqDepartment of Medicine, King Edward Medical University, Lahore 54000, Punjab, Pakistan.
Rania Usman LatifDepartment of Medicine, King Edward Medical University, Lahore 54000, Punjab, Pakistan.
Saim AmirDepartment of Medicine, King Edward Medical University, Lahore 54000, Punjab, Pakistan.
Abdul BasitDepartment of Medicine, King Edward Medical University, Lahore 54000, Punjab, Pakistan.
Abdul M BasilDepartment of Medicine, Spinghar Medical University, Kabul 1001, Kābul, Afghanistan. abdulmaboodbasil@outlook.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute disseminated encephalomyelitis (ADEM), which is rare, primarily affects children. It usually manifests as acute encephalopathy and multifocal neurological impairments after infection or vaccination. Diagnosis is still difficult due to the clinical and radiological similarity to other central nervous system disorders. Adult-onset ADEM calls for thorough reporting in order to improve diagnosis and treatment. CASE SUMMARY: A 55-year-old man with hypertension had a high fever, intense headache and a steady decline in his neurological function after two weeks. Left facial paralysis was the initial symptom, which progressed to left hemiparesis, reduced consciousness level, photophobia, phonophobia, vomiting, and a focal seizure in the right leg. He had no history of autoimmune disease, vaccinations, or infections. Investigations showed negative infectious/autoimmune serology, mild cerebrospinal fluid lymphocytic pleocytosis (protein 76 mg/dL), and lymphopenia. Brain magnetic resonance imaging without contrast revealed bilateral, symmetrical T2/fluid-attenuated inversion recovery hyperintensities, primarily in the middle cerebellar peduncles, with minor involvement in the pontine and periventricular regions. Neoplastic, metabolic, vascular, and infectious conditions were not included. The patient showed spontaneous neurological improvement by Week 3 with near-complete motor recovery (limb strength 4/5) after methylprednisolone and rehabilitation, despite logistical delays in starting immunotherapy. The monophasic course and radiological/clinical remission were supported by idiopathic ADEM.

conclusionThis case shows an uncommon, idiopathic, cerebellar-predominant ADEM variation in an adult without conventional triggers. It emphasizes the diagnostic difficulty in distinguishing ADEM from mimics (such as stroke or infection) in adults. Spontaneous improvement before treatment, although early detection is still crucial, should be highlighted, although early detection is still crucial. Increased clinician awareness, fair access to neuroimaging, and focused research on adult ADEM are crucial to fill these gaps and improve outcomes in places with limited resources.

Indexed as

Acute disseminated encephalomyelitisAdult-onset acute disseminated encephalomyelitisCase reportCentral nervous system inflammationDemyelinating disordersEncephalopathyIdiopathic acute disseminated encephalomyelitisImmune-mediated encephalitisMagnetic resonance imaging brain lesionsMultifocal neurological deficits

Identifiers

PMID41113073
PMCPMC12531693

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