[2] Most common is a high-spiking, quotidian (once/day) fever. The rash frequently appears during febrile attacks and may last for several hours after defervescence, leading to its evanescent character. Adult-onset Still’s disease (AOSD) is a systemic inflammatory disorder of unknown etiology, characterized by evanescent non-pruritic, maculopapular, salmon-pink skin rash, spiking fever, arthralgias or arthritis, and leukocytosis (>10000mm 3) with at least 80% neutrophils.Other signs and symptoms include sore throat, lymphadenopathy, … The classic rash is an evanescent, salmon pink, macular or maculopapular eruption, which usually appears with the fever spike. More than 99% of patients with AOSD manifest with fever > 39° C at some time during the course of their disease. Acute-phase reactants, including ESR, CRP, and serum ferritin are markedly elevated in AOSD. An important diagnostic finding in adult JRA is the presence of a double quotidian fever, which occurs in few other disorders. Four cardinal symptoms are quotidian spiking fever, joint involvement, evanescent salmon pink-rash rash, and leukocytosis with neutrophilia. Please enter a Recipient Address and/or check the Send me a copy checkbox. Results: Fourteen biopsy specimens were studied from seven women and three men with a mean age of 44.4 years. A salmon-colored evanescent rash with fever in a young male along with arthralgias, hepatosplenomegaly, elevated LFTs and negative ANA among others (meeting all Yamaguchi criteria) established diagnosis of Adult-Onset Still’s disease (AOSD). Typically salmon-colored and maculopapular, it is most prominent on the extremities (extensor surfaces), trunk, neck, and, rarely, on the face. Treatment includes NSAIDs, glucocorticoids, DMARDs such as methotrexate, and IL-1 inhibitors. The typical skin rash of AOSD is an evanescent salmon-pink non-pruritic or mildly pruritic maculopapular rash, with nonspecific histologic characteristics comprised of a superficial perivascular lymphocytic and scattered neutrophilic infiltrate in the upper epidermis [11–13]. The rash occurs with fever and subsides with defervescence. Febrile spikes are often accompanied by exacerbation of other systemic manifestations. Burnout Might Really Be Depression; How Do Doctors Cope? Arthritis completes the common triad of AOSD; however, its presence and extent is often less evident at the onset of disease. This website also contains material copyrighted by 3rd parties. You've successfully added to your alerts. Later, ferritin resulted at 15,120 ng/mL while BM biopsy BAL cultures and cytology were negative. Systemic-onset juvenile rheumatoid arthritis is sometimes associated with an evanescent salmon-pink rash on the trunk. Some reports indicate a predilection for women. Psoriasis Clinical Practice Guidelines (AAD/NPF, 2021), Surgeon Calls Into Virtual Court Trial During Operation, Applying Lessons From Oprah to Your Practice, Emerging Treatments for Molluscum Contagiosum and Acne Show Promise. Nevertheless, AOSD is a rare diagnosis, and infection and malignancy must be excluded. Low-grade or atypical fever patterns are sometimes encountered in older patients (> 35 years). Values of 3000-30,000 mg/mL have often been reported in association with the onset and/or flare of disease activity.[6,7,8,9]. Mouth tightening. A transient, evanescent, salmon-colored macular or maculopapular skin rash. [2] Hyperferritinemia may be of diagnostic value in assessing patients with AOSD. Still other individua… Adult onset Still's disease (AOSD) is a systemic inflammatory disease with unknown etiology and characterized by evanescent salmon pink rash, sore throat, liver dysfunction, lymphadenopathy, hepatosplenomegaly, arthritis, and leukocytosis. Symptoms and signs include daily high spiking fever, evanescent salmon-colored rash on the trunk and extremities, arthritis, lymphadenopathy, and leukocytosis. Please use this form to submit your questions or comments on how to make this article more useful to clinicians. Adult-onset Still's disease (AOSD) is a systemic inflammatory disease of uncertain etiology. RATIONALE: Adult-onset Still disease (AOSD) is a rare systemic inflammatory disease of unknown etiology characterized by evanescent salmon-pink rash, fever spikes, arthralgia, and lymphadenopathy. Characteristic manifestations include preceding sore throat, fever, evanescent rash, arthritis/serositis, leukocytosis, and negative serologic testing for antinuclear antibodies (ANA) and rheumatoid factor (RF).[1]. The lesions often develop on the extremities and over the trunk [2] Urticarial forms have been described. Typically, patients with adult Still's disease present with liver/spleen involvement, posi-articular arthritis, ocular involvement, and evanescent salmon-colored truncal rash. See table below for diagnostic criteria. Methotrexate is used in the management, but anakinra is preferred in the systemic variant. It is predominantly found on the proximal limbs and trunk , . It is rare for AOSD to present with arthritis prior to the onset of other systemic manifestations. If you log out, you will be required to enter your username and password the next time you visit. The diagnosis of AOSD is often problematic, because there is no single diagnostic test or pathognomonic histopathology. Sore throat can be an early symptom of AOSD. AOSD usually has a good prognosis, but it can sometimes be fatal, especially when it is complicated by systemic Bottom Line: Adult onset Still's disease (AOSD) is a systemic auto-inflammatory condition of unknown etiology, characterized by high fever, an evanescent, salmon-pink maculopapular skin rash, arthralgia or arthritis and leukocytosis.AOSD can also present with atypical cutaneous manifestations, such as persistent pruritic coalescent papules or plaques and linear lesions … Most patients respond to therapy, and prognosis of AOSD with treatment is good. The symptoms are transient, leave no deformity, and may precede the purpuric rash in 15 to 25 percent of patients. Change ), You are commenting using your Google account. Please see our. In some cases, a new episode does not occur or does not occur until many years later. It is considered one of the major Yamaguchi's criteria in adult-onset Still's disease. To our knowledge, the histopathology of evanescent salmon-pink rash has not been cleared. Table 1 A fever is likely to occur with roseola, erythema infectiosum (fifth disease), and The rash occurs in about 73% of patients, and it is predominantly found on the proximal limbs and trunk: it can be mildly pruritic (32% of the patients according to a Dutch study), and may be mistaken for a drug allergy. The skin lesions were typically erythematous macules, papules, or plaques with a median duration of 5 weeks. an acute systemic inflammatory disorder that is characterized by high spiking fevers, an evanescent salmon-colored rash, Autoimmune connective tissue disease associated with rash: Juvenile idiopathic arthritis and adult-onset Still disease: Rash consists of evanescent, salmon pink maculopapular rash occurring with fever. Ischemic Stroke May Hint at Underlying Cancer, Topol: US Betrays Healthcare Workers in Coronavirus Disaster, The 6 Dietary Tips Patients Need to Hear From Their Clinicians. Because childhood rashes may be difficult to differentiate by appearance alone, it is important to consider the entire clinical presentation to help make the appropriate diagnosis. Evanescent salmon-pink rash, arthralgias, arthritis, myalgias, cervical adenopathy, sore throat, cough, chest pain ANA, RF, serum ferritin concentration, x-rays of affected joints Giant cell (temporal) arteritis However, atypical skin lesions are also described. Typical skin rash is an evanescent, salmon-pink erythema predominantly involving extremities, which is included as one of the diagnostic criteria; however, recent findings show that not only typical evanescent rash but also various skin lesions are associated with AOSD. You will receive email when new content is published. [10], Medscape Dermatology. Click the topic below to receive emails when new articles are available. Criteria for the diagnosis of AOSD have been developed by several investigators. The typical Still rash is an evanescent, salmon-pink, maculopapular eruption that has been reported in up to 87% of patients with AOSD (3) and is well accepted as a major diagnostic criterion (2). Patients may suffer from extended delays in diagnosis and protracted and costly efforts to exclude occult infection or neoplasm. . ( Log Out / Battle of the Sexes: Who Gives Better Medical Care? Over 90% of AOSD patients have an ESR > 50 mm/hr, and half have an ESR > 90 mm/hr. In a subset of patients, in addition to evanescent salmon-pink rash on the trunk and lower legs, more persistent pruritic papules, and plaques develop on the trunk, neck, face, or extensor aspect of the limbs. Systemic-onset JIA is usually accompanied by an evanescent rash (lasting a few hours), which is typically nonpruritic, macular, and salmon colored on the trunk and extremities. Dermatologic Manifestations of Pulmonary Disease. Change ), You are commenting using your Twitter account. The classic presentation of adult JRA is daily high fevers accompanied by an evanescent salmon colored rash on the trunk along with myalgias and polyarticular arthritis. [3] The rash frequently appears during febrile attacks and may last for several hours after defervescence, leading to its evanescent character. You must declare any conflicts of interest related to your comments and responses. Other individuals may develop chronic disease, in which episodes come and go, often years apart and with no symptoms in-between episodes. Adult onset Still’s disease (AOSD) is a systemic auto-inflammatory condition of unknown etiology, characterized by intermittent spiking high fever, an evanescent, salmon-pink or erythematous maculopapular skin rash, arthralgia or arthritis and leukocytosis with at least 80 % neutrophils [].Other common symptoms include sore throat, lymphadenopathy, hepatomegaly, and … Change ), You are commenting using your Facebook account. Symptoms and signs include daily high spiking fever, evanescent salmon-colored rash on the trunk and extremities, arthritis, lymphadenopathy, and leukocytosis. Considerations include the appearance and location of the rash; the clinical course; and associated symptoms, such as pruritus or fever. It is most commonly diagnosed in young adults (median age, 36 years) but has been described in older age groups. Adult-onset Still Disease (AOSD) is a rare disorder that affects multiple organ systems. AOSD should be considered in the evaluation of undiagnosed fever of unknown origin, particularly if present in association with rheumatic complaints. 2003;4(1) © 2003 Medscape. Cite this: Evanescent Maculopapular Eruption in a Woman With Fever and Joint Aches - Medscape - May 05, 2003. Koebnerization and dermatographism are characteristic. The distinctive "rheumatoid rash" or "Still's rash" was first described by Boldero in 1933. Biopsy of the rash reveals nonspecific perivascular infiltrates, often with a predominance of neutrophils, similar to that seen in other rheumatic conditions. Evanescent rash. Adult-onset Still's Disease is a rare, idiopathic, inflammatory disorder characterized by arthralgia, evanescent, salmon-colored rash, and daily fevers as well as lymphadenopathy, pharyngitis, splenomegaly, myalgias, and serositis. Systemic JIA is characterized by arthritis, an evanescent, salmon pink, macular rash, spiking fever (daily or twice-daily fever to ≥39° C with rapid decrease to normal or subnormal temperatures), hepatosplenomegaly, lymphadenopathy, pericarditis, cervical spine involvement, and significantly increased markers of inflammation. Some individuals may only develop one random episode that responds to treatment and resolves within one year. [4] Isdale and Bywaters demonstrated a strong association between the rash and other characteristic features of Still's disease, including intermittent fever, lymphadenopathy, splenomegaly, leukocytosis, and an elevated ESR.[1,5]. That of Yamaguchi and colleagues appears to demonstrate the greatest sensitivity (96%) and specificity (92%) and is summarized in the D. TNF-α and IL-6 inhibitors may be beneficial, but more studies are needed to establish their efficacy. It occurs in about 70% of the patients before or during the first month of each disease flare. A skin biopsy revealed that rash was The typical skin rash is evanescent, salmon-pink, nonpruritic and maculopapular, predominantly on the extremities. The symptoms, progression and severity of adult onset Stills disease are highly variable from one person to another. It is usually truncal but may involve the extremities; Koebnerization is common. The cause is unknown, but AOSD appears to be a disease of autoinflammation rather than autoimmunity. All material on this website is protected by copyright, Copyright © 1994-2021 by WebMD LLC. The absence of interface reaction at the dermoepidermal junction may be helpful in excluding other connective tissue diseases. Fill in your details below or click an icon to log in: You are commenting using your WordPress.com account. Introduction. To comment please, Comments on Medscape are moderated and should be professional in tone and on topic. Marked hyperferritinemia is a characteristic finding of AOSD and has been regarded as a marker of disease activity (4). Scleroderma Sclerodactyly. ( Log Out / Please confirm that you would like to log out of Medscape. ( Log Out / The rash predominantly involves the trunk and extremities but can also involve the palms, soles, and occasionally the face. Skin thickening and hardening, giving the skin a shiny appearance and leading to curling of the fingers with loss of mobility. The characteristic rash of adult Still's disease is described as an evanescent salmon pink, macular or maculopapular eruption, classically appearing only during febrile episodes.
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