2019
DOI: 10.1055/s-0039-1693008
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Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Abstract: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a relatively common autoimmune disorder affecting the peripheral nerves and nerve roots, often causing progressive or recurrent weakness with diminished reflexes. Electrodiagnostic (EDx) studies, cerebral spinal fluid (CSF) analysis, and nerve biopsy may help provide supportive evidence for the diagnosis. Most cases have a favorable response to one of the three first-line treatments: corticosteroids, IV immunoglobulin (IVIG) and plasmapheresis… Show more

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Cited by 6 publications
(5 citation statements)
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References 157 publications
(151 reference statements)
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“…The progressive phase lasted more than 3 months. Furthermore, this patient responded to corticosteroid treatment, one of the characteristics of CIDP ( 29 ). Therefore, there was sufficient evidence to confirm a CIDP diagnosis for the patient.…”
Section: Discussionmentioning
confidence: 82%
“…The progressive phase lasted more than 3 months. Furthermore, this patient responded to corticosteroid treatment, one of the characteristics of CIDP ( 29 ). Therefore, there was sufficient evidence to confirm a CIDP diagnosis for the patient.…”
Section: Discussionmentioning
confidence: 82%
“…CIDP is an acquired demyelinating disease involving the peripheral nerves and is seen as a chronic counterpart to AIDP. 34 Differentiation from AIDP is important as CIDP has a satisfactory treatment response to corticosteroids, immunomodulators, intravenous immunoglobulin (IVIG), and plasma exchange. 35 While usually a clinical diagnosis, MRI can be differentiating.…”
Section: Methodsmentioning
confidence: 99%
“…35 While usually a clinical diagnosis, MRI can be differentiating. 34 Acute phase imaging may demonstrate diffuse enhancement and hyperintense T2-weighted signal amongst intra-and extradural spinal nerves and branches (Figure 5); chronic phase imaging may show atrophy and fatty involution of the affected muscle groups. 36 Glial fibrillary acidic protein astrocytopathy.…”
Section: Methodsmentioning
confidence: 99%
“…Methotrexate was ineffective in a survey where intravenous immunoglobulin or corticosteroids were administrated as maintenance therapy [45]. The usual dose of intravenous immunoglobulin is 2 g/kg bodyweight for 2-5 days.…”
Section: Treatmentmentioning
confidence: 99%