Abstract |
Inflammatory demyelinating neuropathies have been associated with membranous and focal sclerosing glomerulonephritis. Here we describe a 58 year old man with a clinical history, physical examination and laboratory investigations consistent with chronic inflammatory demyelinating polyradiculoneuropathy ( CIDP), who also had severe lower limb and sacral oedema resistant to medical therapy. Mild proteinuria was present and a renal biopsy showed features consistent with focal sclerosing glomerulonephritis (FSGN). The patient's weakness and oedema did not respond to i.v. immunoglobulin or plasmapheresis but responded to high dose oral prednisone. The oedema was not explained by immobility, hypoproteinaemia or local factors. The occurrence of the oedema in a person with CIDP and FSGN and its improvement with prednisone, together with improvement in CIDP and FSGN, suggests that it was immune mediated, possibly due to increased capillary permeability. The presence of renal disease in patients with inflammatory demyelinating neuropathies may be more common than currently realised.
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Authors | R D Henderson, H G Healy, P A McCombe, C M Lander |
Journal | Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
(J Clin Neurosci)
Vol. 7
Issue 2
Pg. 148-9
(Mar 2000)
ISSN: 0967-5868 [Print] Scotland |
PMID | 10844803
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright 2000 Harcourt Publishers Ltd. |
Chemical References |
- Anti-Inflammatory Agents
- Prednisone
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Topics |
- Anti-Inflammatory Agents
(therapeutic use)
- Edema
(drug therapy, etiology)
- Glomerulosclerosis, Focal Segmental
(complications, drug therapy)
- Humans
- Kidney Glomerulus
(drug effects, physiopathology)
- Male
- Middle Aged
- Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
(complications, drug therapy)
- Prednisone
(therapeutic use)
- Sacrococcygeal Region
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