Raynaud's phenomenon
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Raynaud's phenomenon
Classification and alien resources

Hands with Raynaud's phenomenon
ICD-10 I73.0
ICD-9 443.0
DiseasesDB 25933
eMedicine med/1993
MeSH D011928

In medicine, Raynaud's phenomenon (pronounced /reɪˈnoʊz/, us dict: rā·nōz′) is a vasospastic ataxia causing birthmark of the fingers, toes, and occasionally added extremities. This action can aswell could could could could could could could could could cause nails to become breakable with longitudinal ridges. Named for French physician Maurice Raynaud (1834–1881), the could could could could could could could could could cause of the abnormality is believed to be the aftereffect of vasospasms that abatement claret accumulation to the corresponding regions. Emotional stress and algid are archetypal triggers of the phenomenon.

It comprises both Raynaud's disease (also accepted as "Primary Raynaud's phenomenon"1), breadth the abnormality is idiopathic,2 and Raynaud's syndrome (secondary Raynaud's), breadth it is acquired by some added instigating factor. Measurement of hand-temperature gradients is one apparatus acclimated to analyze amid the primary and accessory forms.3

It is accessible for the primary anatomy to advance to the accessory form.4

In acute cases, the accessory anatomy can advance to necrosis or gangrene of the fingertips.

Raynaud's abnormality is an exaggeration of vasomotor responses to algid or affecting stress. Added specifically, it is a hyperactivation of the sympathetic system causing acute vasoconstriction of the borderline claret vessels, arch to tissue hypoxia. Chronic, alternate cases of Raynaud abnormality can aftereffect in decline of the skin, subcutaneous tissues, and muscle. It can aswell rarely could could could could could could could could could cause ulceration and ischemic gangrene.5

Contents

Symptoms

The action can could could could could could could could could could cause affliction aural the afflicted extremities, birthmark (paleness) and sensations of algid and/or numbness. This can generally be cutting to those who are not diagnosed, and sometimes it can be obstructive. If anyone with Raynaud's is placed in too algid a climate, it could potentially become dangerous.

The affection cover several circadian blush changes:

  1. When apparent to algid temperatures, the blood accumulation to the fingers or toes, and in some cases the adenoids or earlobes, is clearly reduced; the derma turns anemic or white (called pallor), and becomes algid and numb.
  2. When the oxygen accumulation is depleted, the derma colour turns dejected (called cyanosis).
  3. These contest are episodic, and if the adventure subsides or the breadth is warmed, the claret breeze allotment and the derma colour aboriginal turns red (rubor), and again aback to normal, generally accompanied by swelling and tingling.

All three colour changes are empiric in archetypal Raynaud's. However, not all patients see all of the above colour changes in all episodes, abnormally in milder cases of the condition. Affection are anticipation to be due to acknowledging hyperemias of the areas beggared of claret flow.

In pregnancy, this assurance frequently disappears due to added apparent blood flow. Raynaud's has aswell occurred in breastfeeding mothers, causing nipples to about-face white and become acutely painful.6 Nifedipine, a calcium approach blocker and vasodilator was recommended to access claret breeze to the extremities and acutely adequate affliction to the breast, in an acutely baby abstraction group.7

Prevalence

The abnormality is added accepted in women than men, with the Framingham Study award that 5% of men and 8% of women ache from it.verification needed

Epidemiology

It is important to analyze Raynaud's disease from syndrome. In adjustment to diagnose these two forms of Raynaud's, a doctor may attending for signs of arthritis or vasculitis, and may conduct a amount of laboratory tests.

Primary Raynaud's (disease)

Raynaud's disease, or "Primary Raynaud's", is diagnosed if the affection are idiopathic, that is, they action by themselves and not in affiliation with added diseases. Some accredit to Primary Raynaud's ache as "being allergic to coldness". It generally develops in adolescent women in their adolescence and aboriginal adulthood. Primary Raynaud's is anticipation to be at atomic partly hereditary, although specific genes accept not yet been identified.8

Smoking worsens abundance and acuteness of attacks, and there is a hormonal component. Caffeine aswell worsens the attacks. Sufferers are added acceptable to accept migraine and angina than controls.

Secondary Raynaud's (syndrome)

Raynaud's syndrome, or "Secondary Raynaud's", occurs secondary to a advanced array of added conditions. Accessory Raynaud's has a amount of associations:

It is important to apprehend that Raynaud's can herald these diseases by periods of added than 20 years in some cases, authoritative it finer their aboriginal presenting symptom. This can be the case in the CREST syndrome, of which Raynaud's is a part.

Patients with Accessory Raynaud's can aswell accept affection accompanying to their basal diseases. Raynaud's abnormality is the antecedent affirmation that presents for 70% of patients with scleroderma, a derma and collective disease.

Raynaud's abnormality which is bound to one duke (or to one foot) is referred to as Unilateral Raynaud's. This is an aberrant form, and it is consistently accessory to bounded or bounded vascular disease. It frequently progresses aural several years to affect added limbs as the vascular ache progresses.11

Examination

A accurate history will generally acknowledge whether the action is primary or secondary. Once this has been established, an assay is abundantly to analyze or exclude accessible accessory causes.

Treatment

Treatment options are abased on the blazon of Raynaud's present. Raynaud's affection is advised primarily by acclamation the basal cause, but includes all options for Raynaud's ache as well. Analysis of primary Raynaud's focuses on alienated triggers:

General care

Emergency measures

Drug therapy

Surgical Intervention


Alternative and Experimental (Research) Approaches

See also

Footnotes

  1. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0. page needed
  2. ^ Raynaud disease at Dorland's Medical Dictionary
  3. ^ Anderson ME, Moore TL, Lunt M, Herrick AL (March 2007). "The 'distal-dorsal difference': a thermographic constant by which to differentiate amid primary and accessory Raynaud's phenomenon". Rheumatology 46 (3): 533–8. doi:10.1093/rheumatology/kel330. PMID 17018538. 
  4. ^ Hirschl M, Hirschl K, Lenz M, Katzenschlager R, Hutter HP, Kundi M (June 2006). "Transition from primary Raynaud's abnormality to accessory Raynaud's abnormality articular by analysis of an associated disease: after-effects of ten years of -to-be surveillance". Arthritis and Rheumatism 54 (6): 1974–81. doi:10.1002/art.21912. PMID 16732585. 
  5. ^ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic base of disease. St. Louis, Mo: Elsevier Saunders. p. 542. ISBN 0-7216-0187-1. 
  6. ^ Holmen OL, Backe B (2009). "An underdiagnosed could could could could could could could could could cause of nipple affliction presented on a camera phone". BMJ 339: b2553. doi:10.1136/bmj.b2553. 
  7. ^ Anderson JE, Held N, Wright K (April 2004). "Raynaud's abnormality of the nipple: a treatable could could could could could could could could could cause of aching breastfeeding". Pediatrics 113 (4): e360–4. doi:10.1542/peds.113.4.e360. PMID 15060268. 
  8. ^ Pistorius MA, Planchon B, Schott JJ, Lemarec H (February 2006). "[Heredity and abiogenetic aspects of Raynaud's disease"] (in French). Journal Des Maladies Vasculaires 31 (1): 10–5. PMID 16609626. http://www.masson.fr/masson/MDOI-JMV-01-2006-31-1-0398-0499-101019-200517601. 
  9. ^ Gayraud M (January 2007). "Raynaud's phenomenon". Joint, Bone, Spine 74 (1): e1–8. doi:10.1016/j.jbspin.2006.07.002. PMID 17218139. 
  10. ^ Berlin AL, Pehr K (March 2004). "Coexistence of erythromelalgia and Raynaud's phenomenon". Journal of the American Academy of Dermatology 50 (3): 456–60. doi:10.1016/S0190-9622(03)02121-2. PMID 14988692. 
  11. ^ Priollet P (October 1998). "[Raynaud's phenomena: analytic and analysis study]" (in French). La Revue Du Praticien 48 (15): 1659–64. PMID 9814067. 
  12. ^ Kahan A, Weber S, Amor B, Saporta L, Hodara M, Degeorges M (April 1981). "Nifedipine and Raynaud's phenomenon". Annals of Internal Medicine 94 (4 pt 1): 546. PMID 7212523. 
  13. ^ Kahan A, Weber S, Amor B, Saporta L, Hodara M, Degeorges M (April 1982). "[Controlled abstraction of nifedipine in the analysis of Raynaud's phenomenon]" (in French). Revue Du Rhumatisme et Des Maladies Ostéo-articulaires 49 (5): 337–43. PMID 6285445. 
  14. ^ Smith CR, Rodeheffer RJ (January 1985). "Raynaud's phenomenon: pathophysiologic appearance and analysis with calcium-channel blockers". The American Journal of Cardiology 55 (3): 154B–157B. doi:10.1016/0002-9149(85)90625-3. PMID 3881908. 
  15. ^ Pancera P, Sansone S, Secchi S, Covi G, Lechi A (November 1997). "The furnishings of thromboxane A2 inhibition (picotamide) and angiotensin II receptor barricade (losartan) in primary Raynaud's phenomenon". Journal of Internal Medicine 242 (5): 373–6. doi:10.1046/j.1365-2796.1997.00219.x. PMID 9408065. 
  16. ^ Dziadzio M, Denton CP, Smith R, et al. (December 1999). "Losartan analysis for Raynaud's abnormality and scleroderma: analytic and biochemical allegation in a fifteen-week, randomized, parallel-group, controlled trial". Arthritis and Rheumatism 42 (12): 2646–55. doi:10.1002/1529-0131(199912)42:12<2646::AID-ANR21>3.0.CO;2-T. PMID 10616013. 
  17. ^ Waldo R (March 1979). "Prazosin relieves Raynaud's vasospasm". JAMA 241 (10): 1037. doi:10.1001/jama.241.10.1037. PMID 762741. 
  18. ^ Fries R, Shariat K, von Wilmowsky H, Böhm M (November 2005). "Sildenafil in the analysis of Raynaud's abnormality aggressive to vasodilatory therapy". Circulation 112 (19): 2980–5. doi:10.1161/CIRCULATIONAHA.104.523324 (inactive 2010-02-15). PMID 16275885. http://circ.ahajournals.org/cgi/content/abstract/112/19/2980. 
  19. ^ Wang WH, Lai CS, Chang KP, et al. (October 2006). "Peripheral sympathectomy for Raynaud's phenomenon: a deliver procedure". The Kaohsiung Journal of Medical Sciences 22 (10): 491–9. doi:10.1016/S1607-551X(09)70343-2. PMID 17098681. 
  20. ^ Neumeister MW, Chambers CB, Herron MS, et al. (July 2009). "Botox analysis for ischemic digits". Plastic and Reconstructive Surgery 124 (1): 191–201. doi:10.1097/PRS.0b013e3181a80576. PMID 19568080. 
  21. ^ Van Beek AL, Lim PK, Gear AJ, Pritzker MR (January 2007). "Management of vasospastic disorders with botulinum adulteration A". Plastic and Reconstructive Surgery 119 (1): 217–26. doi:10.1097/01.prs.0000244860.00674.57. PMID 17255677. 
  22. ^ Muir AH, Robb R, McLaren M, Daly F, Belch JJ (2002). "The use of Ginkgo biloba in Raynaud's disease: a double-blind placebo-controlled trial". Vascular Medicine 7 (4): 265–7. doi:10.1191/1358863x02vm455oa. PMID 12710841. 
  23. ^ Tucker AT, Pearson RM, Cooke ED, Benjamin N (November 1999). "Effect of nitric-oxide-generating arrangement on microcirculatory claret breeze in derma of patients with astringent Raynaud's syndrome: a randomised trial". Lancet 354 (9191): 1670–5. doi:10.1016/S0140-6736(99)04095-7. PMID 10568568. 
  24. ^ Karavidas MK, Tsai PS, Yucha C, McGrady A, Lehrer PM (September 2006). "Thermal biofeedback for primary Raynaud's phenomenon: a analysis of the literature". Applied Psychophysiology and Biofeedback 31 (3): 203–16. doi:10.1007/s10484-006-9018-2. PMID 17016765. 
  25. ^ DiGiacomo RA, Kremer JM, Shah DM (February 1989). "Fish-oil comestible supplementation in patients with Raynaud's phenomenon: a double-blind, controlled, -to-be study". The American Journal of Medicine 86 (2): 158–64. doi:10.1016/0002-9343(89)90261-1. PMID 2536517. 

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