Chronic inflammatory demyelinating polyneuropathy caused by hepatocellular carcinoma

dc.contributor.authorSawma, Tedy
dc.contributor.authorKanso, Mariam
dc.contributor.authorKhalife, Jawad
dc.contributor.authorKhalife, Mohamad Jawad
dc.contributor.departmentSurgery
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:14:39Z
dc.date.available2025-01-24T12:14:39Z
dc.date.issued2023
dc.description.abstractParaneoplastic syndromes are rare abnormal endocrine or immune responses triggered by neoplasms. Chronic inflammatory demyelinating polyneuropathy (CIDP) is one such example. CIDP is an acquired, immune-mediated neuropathy affecting the peripheral nerves and nerve roots. It is associated with many types of cancers, especially haematological malignancies. We report the case of a man in his 60s who presented to the emergency department with acute symptoms of upper and lower extremity paresis and decreased sensation in the toes and tips of his fingers. Laboratory tests were normal. Electrodiagnostic studies showed diffuse motor and sensory dysfunction in all extremities; a diagnosis of CIDP was consequently made. Imaging studies showed a large left lobe liver mass. Subsequent biopsy revealed histopathological findings characteristic of hepatocellular carcinoma. After failure of medical treatment with intravenous immunoglobulin and corticosteroids, laparoscopic resection of the tumour was planned, performed and resulted in complete resolution of symptoms. At 18 months postoperatively, the patient was asymptomatic. © 2023 BMJ Publishing Group Limited.
dc.identifier.doihttps://doi.org/10.1136/bcr-2022-251770
dc.identifier.eid2-s2.0-85147894633
dc.identifier.pmid36764741
dc.identifier.urihttp://hdl.handle.net/10938/33213
dc.language.isoen
dc.publisherBMJ Publishing Group
dc.relation.ispartofBMJ Case Reports
dc.sourceScopus
dc.subjectLiver disease
dc.subjectPeripheral nerve disease
dc.subjectSurgery
dc.subjectBiopsy
dc.subjectCarcinoma, hepatocellular
dc.subjectHumans
dc.subjectImmunoglobulins, intravenous
dc.subjectLiver neoplasms
dc.subjectMale
dc.subjectPolyradiculoneuropathy, chronic inflammatory demyelinating
dc.subjectAntinuclear antibody
dc.subjectBeta2 glycoprotein 1 antibody
dc.subjectCalcium
dc.subjectCorticosteroid
dc.subjectCreatinine
dc.subjectCytokeratin 18
dc.subjectCytokeratin 8
dc.subjectGanglioside antibody
dc.subjectGanglioside gd 1a
dc.subjectGanglioside gd 1b
dc.subjectGanglioside gq 1b
dc.subjectGlypican
dc.subjectHep par 1
dc.subjectImmunoglobulin
dc.subjectMagnesium
dc.subjectMarker
dc.subjectMethylprednisolone sodium succinate
dc.subjectPotassium
dc.subjectRo antibody
dc.subjectSodium
dc.subjectUnclassified drug
dc.subjectAdult
dc.subjectAreflexia
dc.subjectArticle
dc.subjectCancer staging
dc.subjectCase report
dc.subjectChild pugh score
dc.subjectChronic inflammatory demyelinating polyneuropathy
dc.subjectChronic kidney failure
dc.subjectClinical article
dc.subjectComputer assisted tomography
dc.subjectDaily life activity
dc.subjectDiabetes mellitus
dc.subjectElectrodiagnosis
dc.subjectElectromyography
dc.subjectFatty liver
dc.subjectFollow up
dc.subjectHematologic malignancy
dc.subjectHistopathology
dc.subjectHuman
dc.subjectLaparoscopic surgery
dc.subjectLimb weakness
dc.subjectLiver biopsy
dc.subjectLiver cell carcinoma
dc.subjectLiver function test
dc.subjectLiver lobectomy
dc.subjectLower extremity paresis
dc.subjectMiddle aged
dc.subjectMotor dysfunction
dc.subjectMuscle action potential
dc.subjectNeurography
dc.subjectNuclear magnetic resonance imaging
dc.subjectParaneoplastic syndrome
dc.subjectParaproteinemia
dc.subjectParesthesia
dc.subjectPinprick test
dc.subjectPositron emission tomography
dc.subjectProtein electrophoresis
dc.subjectSensation
dc.subjectSensory dysfunction
dc.subjectUltrasound
dc.subjectUpper extremity paresis
dc.subjectVibration
dc.subjectComplication
dc.subjectLiver tumor
dc.subjectPolyradiculoneuropathy
dc.titleChronic inflammatory demyelinating polyneuropathy caused by hepatocellular carcinoma
dc.typeArticle

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