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Research ArticleOriginal Article
Open Access

Idiopathic intracranial hypertension. Atypical presentation

Hussein A. Algahtani, Saleh S. Baeesa, Tahir H. Obeid and Ahmad R. Abuzinadah
Saudi Medical Journal May 2007, 28 (5) 762-765;
Hussein A. Algahtani
Consultant Neurologist, Neurology Division, Department of Medicine, King Khalid National Guard Hospital, PO Box 12723, Jeddah 21483, Kingdom of Saudi Arabia. Tel. +966 (2) 6240000 ext. 1298 / 2070. Fax. +966 (2) 6240000 ext. 2765. E-mail: [email protected]
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Saleh S. Baeesa
Consultant Neurologist, Neurology Division, Department of Medicine, King Khalid National Guard Hospital, PO Box 12723, Jeddah 21483, Kingdom of Saudi Arabia. Tel. +966 (2) 6240000 ext. 1298 / 2070. Fax. +966 (2) 6240000 ext. 2765. E-mail: [email protected]
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Tahir H. Obeid
Consultant Neurologist, Neurology Division, Department of Medicine, King Khalid National Guard Hospital, PO Box 12723, Jeddah 21483, Kingdom of Saudi Arabia. Tel. +966 (2) 6240000 ext. 1298 / 2070. Fax. +966 (2) 6240000 ext. 2765. E-mail: [email protected]
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Ahmad R. Abuzinadah
Consultant Neurologist, Neurology Division, Department of Medicine, King Khalid National Guard Hospital, PO Box 12723, Jeddah 21483, Kingdom of Saudi Arabia. Tel. +966 (2) 6240000 ext. 1298 / 2070. Fax. +966 (2) 6240000 ext. 2765. E-mail: [email protected]
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Abstract

OBJECTIVE: To describe the clinical features of 5 patients with rare atypical presentation of idiopathic intracranial hypertension (IIH), and propose the possible mechanism of this atypical presentation.

METHODS: We carried out a retrospective study of 5 patients admitted at King Khalid National Guard Hospital, Jeddah, Kingdom of Saudi Arabia with IIH during the period from January 2001 to December 2005. All were females with their age ranges from 24 to 40 years. The clinical presentations, and the laboratory and imaging studies were analyzed. The opening pressures of the lumbar puncture tests were documented.

RESULTS: All patients were presented with headache. One had typical pain of trigeminal neuralgia, and one with neck pain and radiculopathy. Facial diplegia was present in one patient, and 2 patients had bilateral 6th cranial neuropathy. Papilledema was present in all patients except in one patient. Imaging study was normal in all patients, and they had a very high opening pressure during lumbar puncture, except in one patient. All patients achieved full recovery with medical therapy in 6 to 12 weeks with no relapse during the mean follow up of 2 years.

CONCLUSION: Atypical findings in IIH are rare and require a high index of suspicion for early diagnosis.

  • Copyright: © Saudi Medical Journal

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Saudi Medical Journal: 28 (5)
Saudi Medical Journal
Vol. 28, Issue 5
1 May 2007
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Idiopathic intracranial hypertension. Atypical presentation
Hussein A. Algahtani, Saleh S. Baeesa, Tahir H. Obeid, Ahmad R. Abuzinadah
Saudi Medical Journal May 2007, 28 (5) 762-765;

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Idiopathic intracranial hypertension. Atypical presentation
Hussein A. Algahtani, Saleh S. Baeesa, Tahir H. Obeid, Ahmad R. Abuzinadah
Saudi Medical Journal May 2007, 28 (5) 762-765;
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© 2025 Saudi Medical Journal Saudi Medical Journal is copyright under the Berne Convention and the International Copyright Convention.  Saudi Medical Journal is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3175. Print ISSN 0379-5284.

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