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A Diagnostic Roadmap for Raynaud's Phenomenon / 대한내과학회지
Korean Journal of Medicine ; : 431-437, 2019.
Article en Ko | WPRIM | ID: wpr-759958
Biblioteca responsable: WPRO
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.
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Texto completo: 1 Índice: WPRIM Asunto principal: Palidez / Estrés Psicológico / Enfermedades de la Tiroides / Capilares / Reperfusión / Anticuerpos Antinucleares / Enfermedades Reumáticas / Educación del Paciente como Asunto / Angioscopía Microscópica / Cianosis Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: Ko Revista: Korean Journal of Medicine Año: 2019 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Palidez / Estrés Psicológico / Enfermedades de la Tiroides / Capilares / Reperfusión / Anticuerpos Antinucleares / Enfermedades Reumáticas / Educación del Paciente como Asunto / Angioscopía Microscópica / Cianosis Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: Ko Revista: Korean Journal of Medicine Año: 2019 Tipo del documento: Article