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Query: UMLS:C0344232 (blurred vision)
 2,072 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A surgically cured case of chronic optochiasmal arachnoiditis presumably caused by concomitant right frontal arteriovenous malformation (AVM) is reported. When a 12-year-old boy, suffering from blurred vision for about 1 month, visited the Ophthalmological Clinic of Hirosaki University Hospital, only a chiasmal lesion was suspected because neuro-ophthalmological examination revealed no more than ophthalmic signs, such as bilateral diminution of vision (Vd, Vs = 0.2), concentric narrowing of visual fields and slight bilateral papilledema. The patient was referred to the Neurosurgical clinic for further examination. Left carotid angiograms showed no abnormalities but, thereafter the brain scintigram revealed an abnormal hot area in the right frontoparietal region. A right carotid angiography demonstreated an AVM in the posterior part of the right frontal lobe. This was fed through the right anterior and middle cerebral arteries and drained into the superior sagittal sinus through meandering dilated cortical vein.
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PMID:[A case of frontal arteriovenous malformation with optochiasmatic arachnoiditis as an initial symptoms (author's transl)]. 103 65

We studied the natural history of patients with a diagnosis of benign coital headache who presented to a private neurological clinic between the years 1978 and 1991. Thirty-two patients (24M, 8F) were invited to participate and 26 patients (83%) responded. The period of follow-up ranged from six months to 14 years (median 6 years). Thirteen patients (50%) had recurrent attacks of coital headache epochs separated by intervals of up to 10 years. Eleven of these patients suffered a concomitant primary headache whereas this was present in only one of those patients without recurrent attacks of coital headache (p < 0.001). In all but one patient, who had a transient blurred vision, the headache was not accompanied by nausea, vomiting, visual disturbances, sensory/motor disturbances, or unconsciousness. We concluded that benign coital headache can be clearly distinguished from headaches due to cerebral aneurysm or arteriovenous malformation rupture. The presence of a concomitant primary headache syndrome is a risk-factor for recurrence of coital headache.
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PMID:Benign coital headache. 147 30

An 8-year-old boy presented with a rare case of optic nerve apoplexy caused by an arteriovenous malformation (AVM) manifesting as severe headache and blurred vision. Computed tomography (CT) showed a hyperdense suprasellar mass. Magnetic resonance (MR) imaging indicated a hematoma in the right optic nerve. MR angiography showed normal vessels. Right fronto-temporal craniotomy identified an aggregate of abnormal, nidus-like vessels adhering to the medial surface of the swollen right optic nerve and a drainer-like ectatic red vein. The diagnosis was probable AVM. To avoid optic nerve damage, the malformation was left intact. Two years later, the boy was readmitted with headache. CT showed bleeding, and angiography revealed feeder arteries and nidus in the suprasellar lesion. The diagnosis was optic nerve apoplexy due to AVM. His symptoms improved without intervention within days. He has not experienced any recurrence of the bleeding for 2 years.
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PMID:Chiasmal and/or optic nerve apoplexy due to rupture of vascular malformation--case report--. 1894 81

Arteriovenous malformation (AVM) is a structural vascular abnormality in which the arterial vasculature connects with the venous vasculature without capillary connections. AVM confined to the nasal cavity is considerably rare. Blurred vision can be one of the associated symptoms. A combined approach of complete surgical resection with prior superselective embolization is the treatment of choice. Following resection, the reconstruction of facial defects, particularly in the nasal area, is challenging. The present study reports the rare case of a patient with an AVM in the nasal cavity, in which embolization, resection and flap reconstruction were performed. Embolization and complete surgical resection were used to avoid recurrence. Subsequently, a combination of free radial forearm and forehead flaps was used for the reconstruction of the nasal defect, without prosthesis. To the best of our knowledge, this is the first report of AVM confined to the nasal cavity, managed by a combination of free radial forearm and forehead flap reconstruction following complete resection. The cosmetic results of the procedure were acceptable.
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PMID:Radial forearm and forehead flap reconstruction following resection of a nasal arteriovenous malformation: A case report. 2769 72