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Office evaluation and treatment of Raynaud's phenomenon
- Source :
- Cleveland Clinic Journal of Medicine. 62:51-61
- Publication Year :
- 1995
- Publisher :
- Cleveland Clinic Journal of Medicine, 1995.
-
Abstract
- BACKGROUND Raynaud9s phenomenon, an episodic vascular disorder induced by cold temperatures or stress and characterized by white, blue, and red discoloration of the fingers and toes, may affect up to 20% of the general population. KEY POINTS Raynaud9s phenomenon may exist independently (primary) or in association with an underlying disease (secondary), most commonly systemic sclerosis. The pathophysiologic features include vasospasm, endothelial cell changes, vessel obstructive features, and hemorrheologic factors. Raynaud9s phenomenon is the initial manifestation of disease in 70% of patients with systemic sclerosis, in whom it may be present for many years before the development of the connective tissue disease. Patients with primary Raynaud9s phenomenon need only conservative management and should be reassured that digital ischemia and loss of tissue occur extremely rarely. Pharmacologic agents that have been studied include vasodilators, platelet inhibitors, serotonin antagonists, and fibrinolytics. CONCLUSIONS For prognostic and therapeutic reasons, it is important to determine if Raynaud9s phenomenon is associated with an underlying condition and if the patient may develop a connective tissue disease.
- Subjects :
- CREST Syndrome
Male
medicine.medical_specialty
Population
Ischemia
Disease
Diagnosis, Differential
Fingers
Internal medicine
medicine
Humans
Connective Tissue Diseases
education
education.field_of_study
business.industry
Raynaud Disease
Vasospasm
General Medicine
medicine.disease
Connective tissue disease
Pathophysiology
Vascular Disorder
Cardiology
Female
business
Subjects
Details
- ISSN :
- 19392869 and 08911150
- Volume :
- 62
- Database :
- OpenAIRE
- Journal :
- Cleveland Clinic Journal of Medicine
- Accession number :
- edsair.doi.dedup.....6250e8c79dc4cb634bb80dd6895ec264
- Full Text :
- https://doi.org/10.3949/ccjm.62.1.51