Acrocyanosis

Acrocyanosis is persistent blue or cyanotic discoloration of the extremities, most commonly occurring in the hands, although it also occurs in the feet and distal parts of face.[1][2][3][4] Although described over 100 years ago and not uncommon in practice, the nature of this phenomenon is still uncertain.[5] The very term "acrocyanosis" is often applied inappropriately in cases when blue discoloration of the hands, feet, or parts of the face is noted.[1] The principal (primary) form of acrocyanosis is that of a benign cosmetic condition,[2] sometimes caused by a relatively benign neurohormonal disorder.[3] Regardless of its cause, the benign form typically does not require medical treatment. A medical emergency would ensue if the extremities experience prolonged periods of exposure to the cold, particularly in children and patients with poor general health.[3] However, frostbite differs from acrocyanosis because pain (via thermal nociceptors) often accompanies the former condition, while the latter is very rarely associated with pain. There are also a number of other conditions that affect hands, feet, and parts of the face with associated skin color changes that need to be differentiated from acrocyanosis: Raynaud phenomenon, pernio, acrorygosis, erythromelalgia, and blue finger syndrome. The diagnosis may be challenging in some cases, especially when these syndromes co-exist.[1]

Acrocyanosis
Dependent acrocyanosis in Postural orthostatic tachycardia syndrome patient
SpecialtyCardiology 

Acrocyanosis may be a sign of a more serious medical problem, such as connective tissue diseases and diseases associated with central cyanosis. Other causative conditions include infections, toxicities, antiphospholipid syndrome, cryoglobulinemia, neoplasms. In these cases, the observed cutaneous changes are known as "secondary acrocyanosis". They may have a less symmetric distribution and may be associated with pain and tissue loss.[1][2]

Signs and symptoms

Acrocyanosis is characterized by peripheral cyanosis: persistent cyanosis of the hands, feet, knees, or face.[4] The extremities often are cold and clammy and may exhibit some swelling (especially in warmer weather).[1][2] The palms and soles exhibit a wide range of sweating from moderately moist to profuse, but all peripheral pulses should have normal rate, rhythm, and quality.[3][4] Exposure to cold temperatures worsens the cyanosis, while it often improves on warming.[2] Aside from the color changes, patients normally are asymptomatic and therefore there is usually no associated pain. The most common sign, discoloration, usually is what prompts patients to seek medical care.[3][4]

Pathophysiology

The precise mechanism of acrocyanosis is not known.[6] The current line of thinking goes that vasospasms in the cutaneous arteries and arterioles produce cyanotic discoloration, while compensatory dilatation in the postcapillary venules causes sweating. Arteriovenous subpapillary plexus shunting also occurs.[1][2][4] Persistent vasoconstriction at the precapillary sphincter creates a local hypoxic environment, thus releasing adenosine into the capillary bed.[7] Vasospasms force adenosine to enter the capillary bed, where it vasodilates the postcapillary venules.[7] Such differences in vessel tone create a countercurrent exchange system that attempts to retain heat. Profuse sweating would then be caused by an overwhelmed countercurrent exchange system. In addition to adenosine, other hormones may contribute to acrocyanosis such as increase blood levels of serotonin.[8] This would seem to support case studies reporting acrocyanosis as an unusual side effect for pediatric patients taking tricyclic antidepressants, as these medications can inhibit the reuptake of serotonin and thus increase their blood concentrations.[9] Acrocyanosis has been reported in association with many other medications and substances.[1]

Diagnosis

Acrocyanosis is diagnosed clinically, based on a medical history and physical examination; laboratory studies or imaging studies are not necessary. The normal peripheral pulses rule out peripheral arterial occlusive disease, where arterial narrowing limits blood flow to the extremities. Pulse oximetry will show a normal oxygen saturation. Unlike the closely related Raynaud's phenomenon, cyanosis is continually persistent. In addition, there is usually no associated trophic skin changes, localized pain, or ulcerations.[2][4] Capillaroscopy and other laboratory methods may be helpful but only complement clinical diagnosis in unclear cases, especially when connective tissue disorders may be present.[1]

Treatment

There is no standard medical or surgical treatment for acrocyanosis, and treatment, other than reassurance and avoidance of cold, is usually unnecessary. The patient is reassured that no serious illness is present. A sympathectomy would alleviate the cyanosis by disrupting the fibers of the sympathetic nervous system to the area.[3] However, such an extreme procedure would rarely be appropriate. Treatment with vasoactive drugs is not recommended but traditionally is mentioned as optional. However, there is little, if any, empirical evidence that vasoactive drugs (α-adrenergic blocking agents or calcium channel blockers) are effective.[1][2]

Prognosis

While there is no cure for acrocyanosis, patients otherwise have excellent prognosis.[2] Unless acrocyanosis results from another condition (e.g. malignancy, antiphospholipid syndrome, atherosclerosis, acute ischemic limb, bacterial endocarditis), there is no associated increased risk of disease or death, and there are no known complications. Aside from the discoloration, there are no other symptoms: no pain, and no loss of function. Patients can expect to lead normal lives. In secondary acrocyanosis treatment of the primary condition defines outcomes.[1]

Epidemiology

Although there is no definitive reporting on its incidence, acrocyanosis shows prevalence in children and young adults than in patients thirty years of age or older.[3] Epidemiological data suggests that cold climate, outdoor occupation, and low body mass index are significant risk factors for developing acrocyanosis.[10] As expected, acrocyanosis would be more prevalent in women than in men due to differences in BMI.[4] However, the incidence rate of acrocyanosis often decreases with increasing age, regardless of regional climate. It completely resolves in many women after menopause implying significant hormonal influences.[1][10]

Around 50% of patients with POTS experience acrocyanosis of their legs while standing still.[11][12]

In the newborn

Acrocyanosis is common initially after delivery in the preterm and full term newborn.[13] Intervention is typically not required as it is seen as a normal finding. Acrocyanosis can also return in a newborn if a baby is cold, such as after a bath, and is considered normal as well.[14]

See also

References
  1. Kurklinsky AK, Miller VM, Rooke TW. "Acrocyanosis: The Flying Dutchman." Vascular Medicine 2011 Aug;16(4):288-301
  2. Olin, J.W. (2004). Other peripheral arterial diseases. In L. Goldman & D. Ausiello (Eds.), Cecil Textbook of Medicine, 22nd Edition. (Vol 1, pp. 475). Philadelphia: WB Saunders ISBN 0-7216-9653-8
  3. Creager, M.A. & Dzau, V.J. (2005). Vascular diseases of the extremities. In D.L. Kasper, A.S. Fauci, D.L. Longo, E. Braunwald, S.L. Hauser, & J.L Jameson (Eds.), Harrison's Prins of Internal Medicine (16th ed., pp. 1490). New York: McGraw-Hill ISBN 0-07-140235-7
  4. (2006). Peripheral vascular disorders. In R.S. Porter, T.V. Jones, & M.H. Beer (Eds.), Merck Manual of Diagnosis and Therapy (18th ed., ch. 212). New York: Wiley, John & Sons ISBN 0-911910-18-2
  5. Coffman, Jay D. (2006), "Acrocyanosis", Vascular Medicine, Elsevier, pp. 707–710, doi:10.1016/b978-0-7216-0284-4.50055-5, ISBN 978-0-7216-0284-4, retrieved 2021-07-30
  6. "Acrocyanosis". Vascular Medicine: A Companion to Braunwald's Heart Disease: 600–603. 2013-01-01. doi:10.1016/B978-1-4377-2930-6.00049-5.
  7. Guyton, A.C. & Hall, J.E. (2006) Textbook of Medical Physiology (11th ed.) Philadelphia: Elsevier Saunder ISBN 0-7216-0240-1
  8. Carpenter, PK; Morris, D (1990). "Association of acrocyanosis with Asperger's syndrome". Journal of Mental Deficiency Research. 34 (1): 87–90. doi:10.1111/j.1365-2788.1990.tb01519.x. PMID 2325122.
  9. Karakara, I.; Aydoğan, M.; Coşkun, A.; Gökalp, A.S. (2003). "Acrocyanosis as a side effect of tricyclic antidepressants: A case report". The Turkish Journal of Pediatrics. 45 (2): 155–57. PMID 12921305.
  10. Carpentier, P.H. (1998). "Definition and Epidemiology of Vascular Acrosyndromes". Rev Prat. 48 (15): 1641–6. PMID 9814064.
  11. Abou-Diab, Jane; Moubayed, Dina; Taddeo, Danielle; Jamoulle, Olivier; Stheneur, Chantal (2018). "Acrocyanosis Presentation in Postural Orthostatic Tachycardia Syndrome". International Journal of Clinical Pediatrics. 7 (1–2): 13–16. doi:10.14740/ijcp293w. ISSN 1927-1255.
  12. Raj, Satish R. (2006-04-01). "The Postural Tachycardia Syndrome (POTS): pathophysiology, diagnosis & management". Indian Pacing and Electrophysiology Journal. 6 (2): 84–99. ISSN 0972-6292. PMC 1501099. PMID 16943900.
  13. Engle, W.A. & Boyle, D.W. (2005). Delivery room management and transitional care. In L.M. Osborn, T.G. DeWitt, L.R. First, & J.A. Zenel (Eds.), Pediatrics (pp. 1250-61). Philadelphia: Elsevier Mosby ISBN 0-323-01199-3
  14. "Skin Color Changes in the Newborn". Saint Luke's Health System. Retrieved 2020-04-08.
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