Raynaud's phenomenon

Raynaud's phenomenon
Classification and external resources

Hands with Raynaud's phenomenon
ICD-10 I73.0
ICD-9 443.0
OMIM 179600
DiseasesDB 25933
eMedicine med/1993
MeSH D011928

In medicine, Raynaud's phenomenon ( /rˈnz/) is a vasospastic disorder causing discoloration of the fingers, toes, and occasionally other areas. This condition can also cause nails to become brittle with longitudinal ridges. Named for French physician Maurice Raynaud (1814–1881), the phenomenon is believed to be the result of vasospasms that decrease blood supply to the respective regions. Emotional stress and cold are classic triggers of the phenomenon.

It comprises both Raynaud's disease (also known as "Primary Raynaud's phenomenon") where the phenomenon is idiopathic,[1] and Raynaud's syndrome (secondary Raynaud's), where it is caused by some other instigating factor. Measurement of hand-temperature gradients is one tool used to distinguish between the primary and secondary forms.[2]

It is possible for the primary form to progress to the secondary form.[3]

In extreme cases, the secondary form can progress to necrosis or gangrene of the fingertips.

Raynaud's phenomenon is an exaggeration of vasomotor responses to cold or emotional stress. More specifically, it is a hyperactivation of the sympathetic system causing extreme vasoconstriction of the peripheral blood vessels, leading to tissue hypoxia. Chronic, recurrent cases of Raynaud phenomenon can result in atrophy of the skin, subcutaneous tissues, and muscle. In rare cases it can cause ulceration and ischemic gangrene.[4]

Contents

Symptoms

The condition can cause pain within the affected extremities, discoloration (paleness) and sensations of cold and/or numbness. This can often be distressing to those who are not diagnosed, and sometimes it can be obstructive. If someone with Raynaud's is placed in too cold a climate, it could potentially become dangerous.

  1. When exposed to cold temperatures, the blood supply to the fingers or toes, and in some cases the nose or earlobes, is markedly reduced; the skin turns pale or white (called pallor), and becomes cold and numb.
  2. When the oxygen supply is depleted, the skin colour turns blue (called cyanosis).
  3. These events are episodic, and when the episode subsides or the area is warmed, the blood flow returns and the skin colour first turns red (rubor), and then back to normal, often accompanied by swelling, tingling, and a painful "pins and needles" sensation.

All three colour changes are observed in classic Raynaud's. However, not all patients see all of the aforementioned colour changes in all episodes, especially in milder cases of the condition. Symptoms are thought to be due to reactive hyperemias of the areas deprived of blood flow.

In pregnancy, this sign normally disappears due to increased surface blood flow. Raynaud's has also occurred in breastfeeding mothers, causing nipples to turn white and become extremely painful.[5] Nifedipine, a calcium channel blocker and vasodilator was recommended to increase blood flow to the extremities and noticeably relieved pain to the breast, in an extremely small study group.[6]

Prevalence

The phenomenon is more common in women than men, with the Framingham Study finding that 5% of men and 8% of women suffer from Raynaud Phenomenon.

Raynaud phenomenon results from an exaggerated vasoconstriction of digital arteries and arterioles. These vascular changes induce paroxysmal pallor or cyanosis of the digits of the hands or feet; infrequently, the nose, earlobes, or lips can also be involved. Characteristically, the involved digits show red, white, and blue color changes from most proximal to most distal, correlating with proximal vasodilation, central vasoconstriction, and more distal cyanosis. Raynaud phenomenon may be a primary disease entity or be secondary to a variety of conditions.[82]

Primary Raynaud phenomenon (previously called Raynaud disease) reflects an exaggeration of central and local vasomotor responses to cold or emotional stresses. It affects 3% to 5% of the general population and shows a predilection for young women. Structural changes in the arterial walls are absent except late in the course, when intimal thickening can appear. The course of Raynaud phenomenon is usually benign, but when long-standing can result in atrophy of the skin, subcutaneous tissues, and muscles. Ulceration and ischemic gangrene are rare.[83]

In contrast, secondary Raynaud phenomenon refers to vascular insufficiency of the extremities secondary to arterial disease caused by other entities including SLE, Scleroderma, Buerger disease, or even Atherosclerosis. Since Raynaud phenomenon may be the first manifestation of such conditions, any patient with new symptoms should be evaluated. Of these individuals, some 10% will eventually manifest an underlying disease.[7] [8]

Epidemiology

It is important to distinguish Raynaud's disease from syndrome. In order to diagnose these two forms of Raynaud's, a doctor may look for signs of arthritis or vasculitis, and may conduct a number of laboratory tests.

Primary Raynaud's (disease)

Raynaud's disease, or "Primary Raynaud's", is diagnosed if the symptoms are idiopathic, that is, if they occur by themselves and not in association with other diseases. Some refer to Primary Raynaud's disease as "being allergic to coldness". It often develops in young women in their teens and early adulthood. Primary Raynaud's is thought to be at least partly hereditary, although specific genes have not yet been identified.[9]

Smoking worsens frequency and intensity of attacks, and there is a hormonal component. Caffeine also worsens the attacks. Sufferers are more likely to have migraine and angina than controls.

Secondary Raynaud's (syndrome)

Raynaud's syndrome, or "Secondary Raynaud's", occurs secondary to a wide variety of other conditions. Secondary Raynaud's has a number of associations:

It is important to realize that Raynaud's can herald these diseases by periods of more than 20 years in some cases, making it effectively their first presenting symptom. This can be the case in the CREST syndrome, of which Raynaud's is a part.

Patients with Secondary Raynaud's can also have symptoms related to their underlying diseases. Raynaud's phenomenon is the initial symptom that presents for 70% of patients with scleroderma, a skin and joint disease.

When Raynaud's phenomenon is limited to one hand or one foot, it is referred to as Unilateral Raynaud's. This is an uncommon form, and it is always secondary to local or regional vascular disease. It commonly progresses within several years to affect other limbs as the vascular disease progresses.[12]

Examination

A careful medical history will often reveal whether the condition is primary or secondary. Once this has been established, an examination is largely to identify or exclude possible secondary causes.

Treatment

Treatment options are dependent on the type of Raynaud's present. Raynaud's syndrome is treated primarily by addressing the underlying cause, but includes all options for Raynaud's disease as well. Treatment of primary Raynaud's focuses on avoiding triggers.

General care

Emergency measures

Drug therapy

Surgical Intervention

Alternative and Experimental (Research) Approaches

See also

Footnotes

  1. ^ "Raynaud disease" at Dorland's Medical Dictionary
  2. ^ Anderson ME, Moore TL, Lunt M, Herrick AL (March 2007). "The 'distal-dorsal difference': a thermographic parameter by which to differentiate between primary and secondary Raynaud's phenomenon". Rheumatology 46 (3): 533–8. doi:10.1093/rheumatology/kel330. PMID 17018538. 
  3. ^ Hirschl M, Hirschl K, Lenz M, Katzenschlager R, Hutter HP, Kundi M (June 2006). "Transition from primary Raynaud's phenomenon to secondary Raynaud's phenomenon identified by diagnosis of an associated disease: results of ten years of prospective surveillance". Arthritis and Rheumatism 54 (6): 1974–81. doi:10.1002/art.21912. PMID 16732585. 
  4. ^ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease. St. Louis, Mo: Elsevier Saunders. p. 542. ISBN 0-7216-0187-1. 
  5. ^ Holmen OL, Backe B (2009). "An underdiagnosed cause of nipple pain presented on a camera phone". BMJ 339: b2553. doi:10.1136/bmj.b2553. 
  6. ^ Anderson JE, Held N, Wright K (April 2004). "Raynaud's phenomenon of the nipple: a treatable cause of painful breastfeeding". Pediatrics 113 (4): e360–4. doi:10.1542/peds.113.4.e360. PMID 15060268. 
  7. ^ Franks AG, Jr (2009 Nov). "Skin manifestations of internal disease.". The Medical clinics of North America 93 (6): 1265–82. PMID 19932330. 
  8. ^ Loebe, M; Heidrich, H (1988 Oct). "The carpal tunnel syndrome--a disease underlying Raynaud's phenomenon?". Angiology 39 (10): 891–901. PMID 3052182. 
  9. ^ Pistorius MA, Planchon B, Schott JJ, Lemarec H (February 2006). "[Heredity and genetic 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. 
  10. ^ Gayraud M (January 2007). "Raynaud's phenomenon". Joint, Bone, Spine 74 (1): e1–8. doi:10.1016/j.jbspin.2006.07.002. PMID 17218139. 
  11. ^ 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. 
  12. ^ Priollet P (October 1998). "[Raynaud's phenomena: diagnostic and treatment study]" (in French). La Revue Du Praticien 48 (15): 1659–64. PMID 9814067. 
  13. ^ 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. 
  14. ^ Kahan A, Weber S, Amor B, Saporta L, Hodara M, Degeorges M (April 1982). "[Controlled study of nifedipine in the treatment of Raynaud's phenomenon]" (in French). Revue Du Rhumatisme et Des Maladies Ostéo-articulaires 49 (5): 337–43. PMID 6285445. 
  15. ^ Smith CR, Rodeheffer RJ (January 1985). "Raynaud's phenomenon: pathophysiologic features and treatment with calcium-channel blockers". The American Journal of Cardiology 55 (3): 154B–157B. doi:10.1016/0002-9149(85)90625-3. PMID 3881908. 
  16. ^ Landry, GJ; Edwards, JM, Porter, JM (1996). "Current management of Raynaud's syndrome.". Advances in surgery 30: 333–47. PMID 8960343. 
  17. ^ Pancera P, Sansone S, Secchi S, Covi G, Lechi A (November 1997). "The effects of thromboxane A2 inhibition (picotamide) and angiotensin II receptor blockade (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. 
  18. ^ Dziadzio M, Denton CP, Smith R, et al. (December 1999). "Losartan therapy for Raynaud's phenomenon and scleroderma: clinical and biochemical findings 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. 
  19. ^ Waldo R (March 1979). "Prazosin relieves Raynaud's vasospasm". JAMA 241 (10): 1037. doi:10.1001/jama.241.10.1037. PMID 762741. 
  20. ^ Fries R, Shariat K, von Wilmowsky H, Böhm M (November 2005). "Sildenafil in the treatment of Raynaud's phenomenon resistant 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. 
  21. ^ Wang WH, Lai CS, Chang KP, et al. (October 2006). "Peripheral sympathectomy for Raynaud's phenomenon: a salvage procedure". The Kaohsiung Journal of Medical Sciences 22 (10): 491–9. doi:10.1016/S1607-551X(09)70343-2. PMID 17098681. 
  22. ^ Neumeister MW, Chambers CB, Herron MS, et al. (July 2009). "Botox therapy for ischemic digits". Plastic and Reconstructive Surgery 124 (1): 191–201. doi:10.1097/PRS.0b013e3181a80576. PMID 19568080. 
  23. ^ Van Beek AL, Lim PK, Gear AJ, Pritzker MR (January 2007). "Management of vasospastic disorders with botulinum toxin A". Plastic and Reconstructive Surgery 119 (1): 217–26. doi:10.1097/01.prs.0000244860.00674.57. PMID 17255677. 
  24. ^ 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. 
  25. ^ Tucker AT, Pearson RM, Cooke ED, Benjamin N (November 1999). "Effect of nitric-oxide-generating system on microcirculatory blood flow in skin of patients with severe Raynaud's syndrome: a randomised trial". Lancet 354 (9191): 1670–5. doi:10.1016/S0140-6736(99)04095-7. PMID 10568568. 
  26. ^ Karavidas MK, Tsai PS, Yucha C, McGrady A, Lehrer PM (September 2006). "Thermal biofeedback for primary Raynaud's phenomenon: a review of the literature". Applied Psychophysiology and Biofeedback 31 (3): 203–16. doi:10.1007/s10484-006-9018-2. PMID 17016765. 
  27. ^ DiGiacomo RA, Kremer JM, Shah DM (February 1989). "Fish-oil dietary supplementation in patients with Raynaud's phenomenon: a double-blind, controlled, prospective study". The American Journal of Medicine 86 (2): 158–64. doi:10.1016/0002-9343(89)90261-1. PMID 2536517. 

External links