Evidence map›Paper›PMID 42130937›Full record

ArticleEuropean journal of case reports in internal medicine2026

Bilateral Peripheral Facial Nerve Palsy: A Rare Clinical Picture.

Tim Geisselmaier, Almir Husic, David Dashti, Kok Sing Tang, David Winkler, Nicolas Geigy, Eliska Potlukova

Abstract read
In one paragraph

Article in European journal of case reports in internal medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited 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

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Tim GeisselmaierDepartment of Internal Medicine, University Center of Internal Medicine, Cantonal Hospital Baselland, Liestal, Switzerland.
Almir HusicDepartment of Internal Medicine, University Center of Internal Medicine, Cantonal Hospital Baselland, Liestal, Switzerland.
David DashtiInstitute of Radiology and Nuclear Medicine, Cantonal Hospital Baselland, Switzerland.
Kok Sing TangNeurology Unit, University Center of Internal Medicine, Cantonal Hospital Baselland, Switzerland.
David WinklerNeurology Unit, University Center of Internal Medicine, Cantonal Hospital Baselland, Switzerland.
Nicolas GeigyEmergency Department, Cantonal Hospital Baselland, Switzerland.
Eliska PotlukovaDepartment of Internal Medicine, University Center of Internal Medicine, Cantonal Hospital Baselland, Liestal, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Bilateral peripheral facial palsy (BPFP) is a rare clinical entity often associated with systemic, infectious, or neurological diseases. Case report: We present a 65-year-old male who developed a severe (House-Brackmann Scale grade VI) sequential BPFP within two weeks, accompanied by hoarseness. His history was remarkable for Crohn's disease in remission, a remote history of relapsing thrombotic thrombocytopenic purpura (TTP), nephrectomy for renal cell carcinoma and currently type 2 diabetes mellitus on insulin. Upon presentation, magnetic resonance imaging of the brain showed contrast enhancement of the facial nerves bilaterally, corresponding to a neuritis facialis, without any signs of stroke or demyelination. The basic laboratory blood tests as well as the cerebrospinal fluid analysis was unremarkable. Extensive laboratory testing showed no signs of infectious and autoimmune causes (Lyme disease, herpes infections, Epstein-Barr virus, human immunodeficiency virus) and no clinical signs of vasculitis, Guillain-Barré syndrome, sarcoidosis, a relapse of TTP or malignancy. Treatment with prednisolone (1 mg/kg body weight) led to clinical improvement (three weeks later House-Brackmann Scale II). The hoarseness disappeared after about three weeks. Conclusions: BPFP is a rare condition requiring a broad differential diagnosis and systematic evaluation. In this patient, type 2 diabetes represented a recognized risk factor, while concomitant hoarseness suggested a possible viral aetiology. Although an association of BPFP with prior TTP has not been reported and with Crohn's disease is exceptional, a shared pathophysiological mechanism cannot be excluded.. LEARNING POINTS: We describe a case of bilateral facial nerve palsy in a patient with history of thrombotic thrombocytopenic purpura and Crohn' s disease.Bilateral facial nerve palsy is a rare neurological condition with a broad differential diagnosis.A detailed patient history and a stepwise diagnostic work-up are essential for identifying underlying systemic or neurological causes.

Indexed as

Bells’ palsybilateral facial nerve palsydiabetes mellitusneuritis cranialisPeripheral facial palsy

Identifiers

PMID42130937
PMCPMC13166995

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.