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Chronic inflammatory demyelinating polyradiculoneuropathy associated intracranial hypertension.

Abstract
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an acquired immune-mediated demyelinating neuropathy. In this report, we detail the course of a 58-year-old male patient who had headache and double vision followed by progressive paresthesia and difficulty in walking. The patient had bilateral papilledema and mild leg weakness, absent ankle jerks and loss of sensation in distal parts of his lower and upper extremities. His electromyography (EMG) was concordant with CIDP and lumbar puncture revealed high opening pressure. The polyradiculoneuropathy as well as the papilledema and elevated cerebrospinal fluid (CSF) pressure improved under steroids. The improvement in intracranial hypertension (IHT) and papilledema under steroid treatment suggests that the IHT in this patient might be associated with CIDP.
AuthorsAyca Altinkaya, Baris Topcular, Nazan Karagoz Sakalli, Demet Yandim Kuscu, Dursun Kirbas
JournalNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (Neurol Sci) Vol. 34 Issue 6 Pg. 1027-9 (Jun 2013) ISSN: 1590-3478 [Electronic] Italy
PMID22941356 (Publication Type: Case Reports, Letter)
Topics
  • Electric Stimulation
  • Electromyography
  • Evoked Potentials, Motor
  • Humans
  • Intracranial Hypertension (diagnosis, etiology)
  • Male
  • Middle Aged
  • Peripheral Nerves (physiopathology)
  • Polyradiculoneuropathy, Chronic Inflammatory Demyelinating (complications, diagnosis)

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