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Vol. 4. Issue. 1. , DOI:. Jul 17, 2017 Secondary Raynaud phenomenon Acrocyanosis, a benign neurohormonal condition, should be included in the differential diagnosis for ability of the clinical course, particularly at the onset of disease, diagnosis may be difficult. For differential diagnosis, the presence of Raynaud phenomenon,. Apr 29, 2004 Comparisons may be useful for a differential diagnosis: Raynaud's disease is a rare disorder characterized by spasms of the blood vessels in Unlike Raynaud phenomenon (RP), acrocyanosis is continually persistent.

Differentialdiagnose raynaud syndrome

Request PDF | On Jan 1, 2006, Ahmadi-Simab K. and others published Differenzialdiagnose des Raynaud-Syndroms und der akralen Ischämiesyndrome | Find, read and cite all the research you need on 2017-08-14 Primary Raynaud syndrome is much more common then secondary Raynaud syndrome. Between 60% and 90% of cases of primary Raynaud syndrome occur in women aged 15 to 40. Anything that stimulates the sympathetic division of the autonomic nervous system , particularly exposure to cold but also strong emotion, can cause arteries to constrict and thus trigger primary Raynaud syndrome. Raynaud’s-type color changes are distinctively different.The disorder has been called Raynaud’s “phenomenon,” “syndrome” or “disease.” Although physicians have used these terms to identify different types, today the words are used interchangeably. Primary Raynaud syndrome is much more common then secondary Raynaud syndrome.

RP has a broad differential but is distinct from acrocyanosis and is differentiated by the Scope of Problem: Raynaud's prevalence is about 8% of men and 11% of women .

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Jahresversammlung vom 12.–14. April 1980 in Wiesbaden), vol 1. Das Raynaud-Syndrom (Abb.

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Wear multiple layers of loose clothing and a hat when it’s cold. The first tip seems pretty obvious but … Primary Raynaud’s disease is much more common and tends to be milder than secondary Raynaud’s. Secondary Raynaud’s (Raynaud’s phenomenon or Raynaud’s syndrome) occurs as a result of an illness or another contributing factor. Symptoms. During an attack of Raynaud’s, symptoms include, but are not limited to, the following: Talk to a Dr. Berg Keto Consultant today and get the help you need on your journey.

According tothe diagnosticcriteria describedabove76patients (55%) could be classified as having a connective tissue disease, the majority having scleroderma (40 patients with scleroderma, 10 patients with CRST syndrome) (Table 1). These 76 patients were con-sidered to have secondary Raynaud's phenomenon. The most common rheumatic disease associations for secondary Raynaud’s include systemic sclerosis (90%), mixed connective tissue disease (85%), and less frequently, Sjögren’s syndrome (33%), systemic lupus erythematosus (10-45%), dermatomyositis and polymyositis (20%), rheumatoid arthritis (10-20%), vasculitis and undifferentiated connective tissue disease. When Raynaud’s occurs, blood cannot reach the surface of the skin, and the affected areas can turn white or blue. In severe cases, loss of blood perfusion can cause sores or even tissue death. The prevalence of Raynaud’s Syndrome is in roughly 5% of the population, with a significantly higher occurrence of Raynaud’s in females. 1998-08-01 All cases of pathognomonic combination of symptoms of a primary disease with physical signs of FR are designated as Raynaud's syndrome (CP).
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Usually the toes and fingers are the primary parts that are affected; however in certain instances, the lips, nipples or nose may also get affected. The attacks are short lived but can occur frequently.
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beim primären Raynaud-Syndrom fehlen Syptome neben der typischen "Anfallssymptomatik" - keine Schmerzen in freien Intervall, keine trophischen Störungen.