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A Diagnostic Roadmap for Raynaud's Phenomenon / 대한내과학회지
Korean Journal of Medicine ; : 431-437, 2019.
Article Dans Coréen | WPRIM | ID: wpr-759958
ABSTRACT
Raynaud's phenomenon (RP) is a reversible vasospasm that is aggravated by cold or emotional stress. Before confirming RP, it is essential to consider other possible causes including compressive neuropathy, sensori-neuropathy, thyroid disease, hematologic conditions and offending drugs. RP is typically characterized by the three-step color change that turns pallor (white), cyanosis (blue), and then erythema (red) of reperfusion. Once RP is diagnosed, it is important to determine whether it is primary or secondary RP. To distinguish primary from the secondary RP, the specialized tests performing in clinical practice are antinuclear antibody (ANA) and nailfold capillary microscopy (NFC). The combination of ANA and NFC is most helpful for discriminating secondary RP due to autoimmune rheumatic disease. Thereby, normal findings of NFC in primary RP distinguished from secondary RP should be understood. Patients with primary RP usually improves with symptomatic treatment focused on lifestyle modification and patient education, but those with secondary RP should be treated together with associated disease or causes.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pâleur / Stress psychologique / Maladies de la thyroïde / Vaisseaux capillaires / Reperfusion / Anticorps antinucléaires / Rhumatismes / Éducation du patient comme sujet / Capillaroscopie / Cyanose Type d'étude: Etude diagnostique Limites du sujet: Humains langue: Coréen Texte intégral: Korean Journal of Medicine Année: 2019 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pâleur / Stress psychologique / Maladies de la thyroïde / Vaisseaux capillaires / Reperfusion / Anticorps antinucléaires / Rhumatismes / Éducation du patient comme sujet / Capillaroscopie / Cyanose Type d'étude: Etude diagnostique Limites du sujet: Humains langue: Coréen Texte intégral: Korean Journal of Medicine Année: 2019 Type: Article