Chonnam Med J.
2002 Dec;38(4):421-425.
Cirrhotic Change after Corticosteroid Therapy in a Patient with Chronic Inflammatory Demyelinating Polyneuropathy
- Affiliations
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- 1Department of Internal Medicine, Chonnam General Hospital, Yosu, Korea. jns9608@naver.com
- 2Department of Neurology, Chonnam General Hospital, Yosu, Korea.
Abstract
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Chronic inflammatory demyelinating polyneuropathy (CIDP) is a symmetrical motor and sensory polyneuropathy with a relapsing or progressive course. It has typical features of elevated CSF protein levels and the electrodiagnostic findings of acquired demyelination. The response to therapy suggests that CIDP is immune-mediated; CIDP responds to glucocorticoids. But long-term adverse effects of steroids including bone demineralization, gastrointestinal bleeding, and cushingoid changes are problematic. A 24 year-old male patient visited our hospital complaining of progressive tingling sensations in his arms and legs. Neurological examination revealed sensory and motor disturbance of the glove-and-stocking type in his all extremities. Cerebrospinal fluid studies showed albumino-cytologic dissociation. Motor nerve conduction studies revealed prolongation of terminal latencies, reduction of conduction velocities, and abnormal temporal dispersion of the motor potentials. No sensory potentials could be evoked at any of the sites stimulated. A diagnosis of CIDP was made, and we started to treat with corticosteroids. His biochemical and radiologic studies at first visit were compatible with chronic active hepatitis due to hepatitis B viral infection. He showed two neurological relapses for nine months. His hepatic dysfunction progressed, and abdominal CT scans showed liver cirrhosis and splenomegaly. Liver biopsy at referred hospital demonstrated liver cirrhosis and regenerating nodules.