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Query: UMLS:C0039483 (giant cell arteritis)
 3,204 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Temporal arteritis is not a common disease, but it is often incorrectly diagnosed in elderly patients with a high ESR and pain in the temporal area. Such an incorrect diagnosis can subject the patient to needless biopsy and the serious side effects of therapy with large doses of prednisone. When temporal arteritis is suspected yet presentation is atypical, careful consideration should be given to ENT and neurologic examination, and even psychiatric evaluation. Temporal artery biopsy should be done on the tender side, with multiple serial sections. A negative biopsy does not rule out temporal arteritis. Therapy should not be deferred until biopsy results are reported. It consists of 40 to 60 mg of prednisone daily for at least four to six weeks with a gradual decrease thereafter.
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PMID:Overdiagnosis of temporal arteritis. 729 57

The Horton's disease is a generalized vascular affectation, characterized by a giant cell arteritis. Medium and small caliber arteries are the most frequently affected, mainly of the craneal vascular territory, in particular the collateral branches of the external carotid, and artery in special the superficial temporal artery. We present a case of lingual necrosis as debut of the Horton's disease that has been diagnosed and treated in our ENT Department.
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PMID:[Tongue necrosis as onset of temporal arteritis]. 1273 23

The first type of facial pain is of vascular origin. Cluster headache is described as well as its subgroups and carotidodynia. Two organic lesions of the arterial wall can also cause facial pain: dissection of the internal carotid artery and giant cell arteritis. Among the facial neuralgias, trigeminal neuralgia is the most frequent. Also, local lesions in the cranial nerves can cause facial pain, as well as organic processes of the upper cervical spine and of the occipitocervical transition. The characteristics of facial pain due to eye or ENT and dental lesions are described. So called atypical facial pain occurs quite frequently and mostly affects middle-aged women.
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PMID:[Facial pain and neuralgias. Diagnosis and treatment.]. 1841 60

The patient is a 67-year-old Caucasian male with a past medical history of diabetes mellitus type 2, coronary artery disease (CAD) status post stent placement, renal cell carcinoma (RCC) status post left nephrectomy and bilateral adrenalectomy secondary to metastatic disease, and aspergillus pneumonia who was transferred from an outside hospital for evaluation of progressively worsening pulsating right temple and retrobulbar headache. Initial studies ruled out glaucoma, giant cell arteritis, and stroke, or aneurysmal pathology. The only positive finding was right sphenoid sinus disease on imaging that had caused bony destruction and infiltration of the right orbital apex. Broad-spectrum antibiotics were started for bacterial versus fungal sinusitis and the patient was admitted to the medical floor with consultations to Neurology, Otolaryngology (ENT), and Ophthalmology. ENT took the patient emergently to the OR. The final diagnosis was chronic aspergillus sinusitis and right-sided orbital apex syndrome (OAS). Antibiotics and antifungals were optimized by the infectious disease team. ENT also ordered steroid washouts post-operatively with budesonide and saline as well as sinus debridements every couple of weeks.
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PMID:More than Meets the Eye: Aspergillus-Related Orbital Apex Syndrome. 3285 Feb 24