Changes of Papilledema in a Case of Idiopathic Intracranial Hypertension
Journal Title: Scholars Journal of Medical Case Reports - Year 2015, Vol 3, Issue 2
Abstract
We present a case of idiopathic intracranial hypertension in an 18-year-old boy. The ophthalmoscopic examination revealed marked papilledema in the right eye and mild papilledema in the left. Magnetic resonance imaging demonstrated a torturous right optic nerve, flattened right posterior sclera, and bilateral enlargement of the optic nerve sheath. The bilateral papilledema worsened during 2 months after the initial visit. On lumbar puncture, the cerebrospinal fluid pressure was 270 mm H2O. He was prescribed acetazolamide, and the bilateral papilledema gradually improved. Six months later, the papilledema was completely resolved.
Authors and Affiliations
Shinji Makino, Shin-ichi Sakamoto
Erythromelalgia- a clinical sign never to be missed
Abstract: Erythromelalgia is a rare clinical condition due to post ganglionic sympathetic dysfunction. Diagnosis of this disorder and differentiating it from other common burning pain syndromes like Raynaud’s phenomenon...
Alopecia due to demodexis
Demodex is a common commensal mite of the pilosebaceous unit in human and animal (mammals). Alopecia is a loss of hair from the head or body and there are many type of hair loss with different symptoms and causes. This i...
Primary Thyroid Lymphoma: a case report
Primary thyroid lymphoma is rare clinical presentation. Most of the cases are subjected to thyroidectomy without proper histological diagnosis. We present a rare case of middle aged lady presenting with rapidly enlarged...
A Rare Case of Neck Abscess Caused by Salmonella paratyphiA
A rare case of neck abscess due to S. paratyphialong with conventional antibiotics resistant was retorted from UT of Dadra & Nagar Haveli, India. The results supports that the S. paratyphiA. is capable to causing both in...
Alobar Holoprosencephaly: about 2 cases and review of the literature
Holoprosencephaly is a rare brain abnormality resulting from an incomplete cleavage of the primitive prosencephalon of forebrain during early embryogenesis. It includes a series of rare complex and heterogenosis disorder...