Idiopathic hypertrophic pachymeningitis: An unusual masquerader of multiple cranial nerve palsies

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منابع مشابه

A case of idiopathic hypertrophic pachymeningitis presenting with chronic headache and multiple cranial nerve palsies

RATIONALE Idiopathic hypertrophic pachymeningitis (IHP) is a rare condition, characterized by a chronic fibrosing inflammatory process usually involving either the intracranial or spinal dura mater, but rarely both. Here, we report a rare case of IHP affecting both the intracranial and spinal dura mater. We also discussed the diagnosis, management, and outcome of IHP. PATIENT CONCERNS We revi...

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Rheumatoid factor positive hypertrophic cranial pachymeningitis in association with hypopituitarism and multiple cranial nerve palsies.

This is the first report of a patient presenting with rheumatoid factor (RF) positive hypertrophic cranial pachymeningitis (HCP) in association with hypopituitarism and multiple cranial nerve palsies. Our patient developed palsies of the left II and III, bilateral VI and VII, and right IX, X, and XII cranial nerves. A stimulation test showed hypopituitarism due to hypothalamic failure. The pati...

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Idiopathic hypertrophic cranial pachymeningitis.

Idiopathic hypertrophic cranial pachymeningitis is a rare form of fibrosing chronic inflammatory process of unknown etiology, which causes thickening of the intracranial dura mater. We present four patients with hypertrophic cranial pachymeningitis who presented with chronic headache and cranial nerve palsies. The diagnosis of idiopathic hypertrophic cranial pachymeningitis was based on neuroim...

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Recurrent multiple cranial nerve palsies.

The material for this paper comprises four case reports, which must necessarily be presented in some detail, having regard to the points in which they resemble and differ from one another. The resemblance between these cases is close enough to suggest that they constitute a recognizable clinical syndrome. As to their aetiology, the data permit no definite conclusion but suggest the possibility ...

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An unusual case of hypopituitarism and recurrent cranial nerve palsies.

We report here the history of a 52-year old woman with diabetes mellitus for 10 years and secondary hypothyroidism (low TSH) who presented with chronic persistent headache for 6 years and sudden onset of complete blindness of 24 hours duration, admitted to our unit at National Hospital of Sri Lanka in July 2004 . On the first admission in 1998, a cranial CT scan demonstrated a lesion suggestive...

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ژورنال

عنوان ژورنال: Journal of Clinical Ophthalmology and Research

سال: 2015

ISSN: 2320-3897

DOI: 10.4103/2320-3897.156607