Synonyms of Kawasaki Disease
- Kawasaki Syndrome
- Mucocutaneous Lymph Node Syndrome
- No subdivisions found.
Kawasaki disease is an acute multisystem inflammatory disease of blood vessels (vasculitis) that most commonly affects infants and young children. The disease may be characterized by a high fever, inflammation of the mucous membranes of the mouth and throat, a reddish skin rash, and swelling of lymph nodes (lymphadenopathy). In addition, individuals with Kawasaki disease may develop inflammation of arteries that transport blood to heart muscle (coronary arteritis), associated widening or bulging (aneurysms) of the walls of affected coronary arteries, inflammation of heart muscle (myocarditis), and/or other symptoms and findings. Kawasaki disease is the primary cause of acquired heart disease in children in the United States. Although the cause of the disease is unknown, it is widely thought to be due to infection or an abnormal immune response to infection.
In many affected children, the initial symptom associated with Kawasaki disease is a high fever that typically rises and falls (remittent fever) and lasts for approximately one to two weeks without treatment. In some cases, fever may persist for up to about three to four weeks. Additional characteristic features include inflammation of the whites of the eyes (bilateral conjunctivitis); inflammation of mucous membranes of the mouth and throat, resulting in dry, red, cracked lips and a strawberry-red tongue; swelling of lymph nodes in the neck (cervical lymphadenopathy); redness and swelling of the hands and feet; and a reddish rash, typically affecting the trunk and often involving the groin area. By about the second or third week, skin tissue may peel (desquamate) from the tips of the fingers and toes and may progress to involve the hands and feet.
In many cases, affected children may have additional symptoms and findings, such as irritability, diarrhea, vomiting, coughing, and/or joint inflammation (arthritis), pain, and swelling. Other associated abnormalities may include enlargement of the liver and spleen (hepatosplenomegaly), inflammation of the protective membranes covering the brain (aseptic meningitis), inflammation of the middle ear (otitis media), and/or other findings.
Many individuals with Kawasaki disease may also have heart (cardiac) involvement. Up to 50 percent may develop inflammation of heart muscle (myocarditis), which may be associated with an abnormally increased heart rate (tachycardia), decreased ventricular (lower heart chamber) functioning, and, in severe cases, impaired ability of the heart to effectively pump blood to the lungs and the rest of the body (heart failure). In addition, in some cases, heart involvement may include inflammation of the membranous sac surrounding the heart (pericarditis), leakage of certain heart valves (aortic or mitral valve insufficiency), or other abnormalities.
The most serious cardiac complication is inflammation of arteries that provide oxygen-rich blood to heart muscle (coronary arteritis) and possible weakening, widening (dilation), and bulging (aneurysms) of affected arterial walls. Dilation and aneurysm formation occur in approximately three to 20 percent of patients. In severe cases, complications may include the development of blood clots in the ballooned area with obstruction of blood flow, bursting (rupture) of an aneurysm, or heart attack, leading to potentially life-threatening complications. Some cases have also been reported in which patients, particularly infants, have fever with fewer than four other features of the disease (see "Diagnosis" below) and subsequently develop coronary artery disease.
Although the exact cause of Kawasaki disease is not known, evidence indicates an infection or an inappropriate immune response to infection. However, despite much research in this area, a specific infectious cause has not been identified.
Recent evidence by Yale University investigators (2005) suggests that a newly discovered coronavirus may have a role in Kawasaki disease. Additional research is needed.
Some researchers suggest that the disease may be caused by certain toxic substances, called bacterial "superantigens," that are produced by particular types of bacteria, such as streptococci or staphylococci. They indicate that such superantigens may trigger an exaggerated response of the immune system, resulting in infiltration of blood vessel walls with certain white blood cells, associated blood vessel inflammation (vasculitis), and cardiovascular damage. However, other researchers suggest that one or more conventional antigens may be involved in causing the inflammatory disease process. (An antigen is any substance that may trigger a particular immune response, such as foreign proteins, including microorganisms.) Further research is necessary to determine the role specific antigens or "superantigens" may play in causing Kawasaki disease.
Kawasaki disease most frequently affects children five years of age or younger. In extremely rare cases, Kawasaki disease may occur during adolescence or adulthood. First reported in Japanese children in the 1960s, the disease is now recognized worldwide and occurs in individuals in all racial and ethnic groups. However, Kawasaki disease appears to affect Asian children most frequently. Estimates indicate that at least 3,000 cases of Kawasaki disease are diagnosed each year in the United States. Males appear to be affected more frequently than females by a ratio of approximately 1.5 to 1.
Symptoms of the following disorders may be similar to those of Kawasaki disease. Comparisons may be useful for a differential diagnosis:
Measles is a highly contagious viral disease occurring primarily in children. Symptoms may include fever, cough, sore throat, runny nose, redness of the eyes (conjunctivitis), and increased sensitivity to light (photophobia). Small red spots with bluish or whitish centers may appear on the inner cheeks (Koplik's spots). In addition, a characteristic red skin rash develops.
Scarlet fever is an infectious disease of childhood caused by toxins produced by Streptococcal bacteria. It may be characterized by fever, vomiting, headache, sore throat, enlarged lymph nodes in the neck, a flushed face, a pale area around the mouth, an inflamed tongue, and a widespread red rash, often with peeling of the skin.
Toxic shock syndrome is a rare infectious disease caused by toxins produced by the bacterium Staphylococcus aureus. Symptoms may include a sudden high fever, vomiting, diarrhea, headache, sore throat, red eyes, and/or a characteristic sunburn-like skin rash with peeling of the skin, particularly of the palms and soles. With disease progression, affected individuals may develop dangerously low blood pressure (hypotension), liver and kidney failure, and dysfunction of other organs. Without early diagnosis and appropriate treatment, life-threatening complications may result. Toxic shock syndrome is most common in menstruating women who use highly absorbent tampons. Other cases have been reported in association with postoperative wound infections, nasal packing, or other factors. (For more information on this disorder, choose "toxic shock" as your search term in the Rare Disease Database.)
A number of additional infectious and non-infectious diseases may be associated with certain symptoms similar to those potentially associated with Kawasaki disease. (For further information on such disorders, choose the exact disease name in question as your search term in the Rare Disease Database.)
Kawasaki disease is diagnosed based on a thorough clinical evaluation; a detailed patient history; and detection of characteristic features, including fever of at least five days and at least four of five characteristic signs (reddened eyes; changes of the lips and mouth; reddish, swollen extremities; rash; and swollen lymph nodes). Laboratory tests may reveal certain non-specific, though characteristic findings, including increased numbers of white blood cells (leukocytosis) and low levels of red blood cells (anemia) during early illness, with a rapidly rising blood platelet count by the second to third week after onset.
In addition, diagnostic tests should be conducted in all individuals with Kawasaki disease to detect possible heart involvement. Such testing may include echocardiography at diagnosis as well as at recommended intervals (e.g., at two to three weeks, six to eight weeks, and potentially six to 12 months after onset). During an echocardiogram, high-frequency sound waves are directed toward the heart, enabling physicians to study cardiac structure and function. Electrocardiograms (EKGs) are often performed along with echocardiograms. An EKG records the electrical activities of heart muscle. For children who develop coronary artery abnormalities, physicians may advise more frequent echocardiography and additional cardiac tests (e.g., stress testing, coronary angiography, and/or other tests). The recommended frequency and the specific tests used during long-term follow-up will be based on various factors, including clinical course, degree of coronary artery involvement, and patient age.
Experts indicate that children with Kawasaki disease should be treated by or in consultation with pediatricians who specialize in the diagnosis and treatment of heart disorders (pediatric cardiologists).
Research has shown that early diagnosis and treatment speeds the resolution of fever and other acute symptoms and significantly lowers the risk of heart damage. Treatment is started as soon as possible after diagnosis and may include high-dose intravenous immune globulin (IGIV) and high-dose aspirin therapy. Immune globulin is a special preparation containing antibodies obtained from the fluid portion of the blood. Evidence indicates that, when given within the first 10 days of onset, IGIV reduces the incidence of coronary artery abnormalities from about 20 percent in patients receiving aspirin alone to three to four percent.
In rare cases, patients may have an insufficient response to initial IGIV treatment and may require re-treatment.
The Food and Drug Administration (FDA) has approved the following IGIV products (immune globulin intravenous [human]) for the treatment of Kawasaki disease: Gammagard S/D, manufactured by Baxter Healthcare; Venoglobulin-S, manufactured by Alpha Therapeutic; Venoglobulin-I, manufactured by Alpha Therapeutic; and Iveegam, manufactured by Baxter Healthcare.
By the 14th day of illness or after resolution of fever, a lower dose of aspirin is typically given for its antiplatelet effect to help prevent blood clots from forming. Such therapy may be continued for up to eight weeks after onset in children without abnormalities detected by echocardiography. However, physicians may advise that aspirin therapy be continued indefinitely for those with coronary artery abnormalities. In some cases, individuals who have multiple or large coronary aneurysms may also receive therapy with anticlotting medications, such as dipyridamole or warfarin.
Due to a small risk of Reye syndrome during outbreaks of flu (influenza) and chickenpox, physicians may recommend annual influenza vaccination for children who require long-term aspirin therapy. (Reye syndrome is a rare disorder of childhood characterized by fatty changes of the liver and acute swelling of the brain. There appears to be an association between the onset of Reye syndrome and the use of aspirin-containing medications [salicylates] in children or adolescents with certain viral illnesses, particularly upper respiratory tract infections [e.g., influenza B] or, in some cases, chickenpox.) If affected children develop symptoms of flu or chickenpox, parents should immediately alert their child's physician, who may recommend temporary interruption of aspirin therapy or temporary substitution with dipyridamole.
In rare cases, coronary artery bypass surgery or heart transplantation may be recommended for individuals with severe heart involvement. Treatment with corticosteroid drugs is not recommended for children with Kawasaki disease. Other treatment for affected individuals is symptomatic and supportive.
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. Government funding, and some supported by private industry, are posted on this government web site.
For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Tollfree: (800) 411-1222
TTY: (866) 411-1010
For information about clinical trials sponsored by private sources, contact:
Organizations related to Kawasaki Disease
Behrman RE, ed. Nelson Textbook of Pediatrics, 16th ed. Philadelphia, Pa: W.B. Saunders Company; 2000:725-27.
Beers MH, et al., eds. The Merck Manual. 17th ed. Whitehouse Station, NJ: Merck Research Laboratories; 1999:2360-63.
Fauci AS, et al., eds. Harrison's Principles of Internal Medicine, 14th Ed. New York, NY: McGraw-Hill, Inc; 1998:1910, 1920.
Berkow R, ed. The Merck Manual-Home Edition. Whitehouse Station, NJ: Merck Research Laboratories; 1997:2360-63.
Bennett JC, Plum F, eds. Cecil Textbook of Medicine. 20th ed. Philadelphia, Pa: W.B. Saunders Company; 1996:2200-01.
Gorbach SL, et al., eds. Infectious Diseases. Philadelphia, Pa: W. B. Saunders Company; 1992:1370-74.
Braunwald E, ed. Heart Disease. A Textbook of Cardiovascular Medicine. 3rd ed. Philadelphia, Pa: W. B. Saunders Company; 1988:1014-16, 1722.
Moran AM, et al. Abnormal myocardial mechanics in Kawasaki disease: rapid response to gamma-globulin. Am Heart J. 2000;139:217-23.
Cunningham MW, et al. Anti-human cardiac myosin autoantibodies in Kawasaki syndrome. J Immunol. 1999;163:1060-65.
Cohen Tervaert JW, et al. The role of superantigens in vasculitis. Curr Opin Rheumatol. 1999;11:24-33.
Jason J, et al. Kawasaki disease and the T-cell antigen receptor. Hum Immunol. 1998;59:29-38.
Marcinkiewicz J, et al. Immunoregulatory mechanisms of action of intravenous gammaglobulin in Kawasaki syndrome. Przegl Lek. 1998;55:611-13.
Choi IH, et al. Clonal expansion of CD8+ T cells in Kawasaki disease. J Immunol. 1997;159:481-86.
Morita A, et al. Serologic evidence that streptococcal superantigens are not involved in the pathogenesis of Kawasaki disease. Microbiol Immunol. 1997;41:895-900.
Leung DY, et al. Evidence for superantigen involvement in cardiovascular injury due to Kawasaki syndrome. J Immunol. 1995;155:5018-21.
Leung DY, et al. The potential role of bacterial superantigens in the pathogenesis of Kawasaki syndrome. J Clin Immunol. 1995;15:11S-17S.
Leung DY, et al. Superantigens in Kawasaki syndrome. Clin Immunol Immunopathol. 1995;77:119-26.
Meissner HC, et al. Kawasaki syndrome. Curr Opin Rheumatol. 1995;7:455-58.
Terai M, et al. The absence of evidence of staphylococcal toxin involvement in the pathogenesis of Kawasaki disease. J Infect Dis. 1995;172:558-61.
Pietra BA, et al. TCR V beta family repertoire and T cell activation markers in Kawasaki disease. J Immunol. 1994;153:1881-88.
Dajani AS, et al. Guidelines for long-term management of patients with Kawasaki disease. Report from the committee on rheumatic fever, endocarditis, and Kawasaki disease, council on cardiovascular disease in the young. American Heart Association. Circulation. 1994;89:916-22.
Kitamura S, et al. Long-term outcome of myocardial revascularization in patients with Kawasaki coronary artery disease. A multicenter cooperative study. J Thorac Cardiovasc Surg. 1994;107:663-73, 673-74.
Albat A, et al. Adult coronary aneurysms related to Kawasaki disease. J Cardiovasc Surg. 1994; 35:57-60.
Leung DY, et al., Toxic shock syndrome toxin-secreting staphylococcus aureus in Kawasaki syndrome. Lancet. 1993;342:1385-88.
Nadel S. Kawasaki disease. Curr Opin Pediatr. 1993;5:29-34.
Dhilon R, et al. Management of Kawasaki disease in the British Isles. Arch Dis Child. 1993;69:631-36, 637-38.
Dundel RP, et al. Kawasaki disease and its cardiac sequelae. Hosp Pract. 1993;28:51-54, 57-60, 64-66.
Ohkuni H, et al. Biologically active extracellular products of oral viridans streptococci and the aetiology of Kawasaki disease. J Med Microbiol. 1993;39:352-62.
Seichshnaydre MA, et al. Kawasaki disease: early presentation to the otolaryngologist. Otolaryngol Head Neck Surg. 1993;108:344-47.
Leung DY. Kawasaki disease. Curr Opin Rheumatol. 1993;5:41-50.
Finberg RW, et al., Effect of high doses of intravenously administered immune globulin on natural killer cell activity in peripheral blood. J Pediatr. 1992;120:376-80.
Akagi T, et al. Outcome of coronary artery aneurysms after Kawasaki disease. J Pediatr. 1992;121:689-94.
Newburger JW, et al. The treatment of Kawasaki syndrome with intravenous gamma globulin. N Engl J Med. 1986;315:341-47.
The information in NORD’s Rare Disease Database is for educational purposes only. It should never be used for diagnostic or treatment purposes. If you have questions regarding a medical condition, always seek the advice of your physician or other qualified health professional. NORD’s reports provide a brief overview of rare diseases. For more specific information, we encourage you to contact your personal physician or the agencies listed as “Resources” on this report.
The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.
Copyright ©1986, 1990, 1991, 1994, 1999, 2000, 2002, 2003, 2009
Report last updated: 2009/04/10 00:00:00 GMT+0
NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.