{"orpha":90397,"name":"Self-healing papular mucinosis","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":[],"definition":"Self-healing papular mucinosis is a rare form of localized lichen myxedematosus occurring primarily in children and characterized by the development of mucinous papules on various parts of the body (face, neck, trunk, and limbs) that resolve spontaneously within some weeks to months. Systemic symptoms can be observed such as fever, arthralgias and weakness.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-90397/","orphanet_url":"https://www.orpha.net/en/disease/detail/90397","names":{"fr":{"name":"Mucinose cutanée juvénile spontanément régressive","definition":"La mucinose cutanée juvénile spontanément régressive est une forme rare de lichen myxodémateux localisé survenant surtout chez les enfants et caractérisée par le développement de papules mucineuses à différents endroits du corps (visage, cou, tronc et membres), et se résolvant de manière spontanée en quelques semaines ou mois. Des symptômes systémiques peuvent être observés, tels qu'une fièvre, des arthralgies et une faiblesse généralisée."},"de":{"name":"Muzinose, papulöse, selbstheilende","definition":"Die selbstheilende papuläre Muzinose ist eine seltene Form des lokalisierten Lichen myxoedematosus (s. dort), die primär bei Kindern auftritt. Sie ist gekennzeichnet durch die Entwicklung muzinöser Papeln in verschiedenen Bereichen des Körpers (Gesicht, Hals, Stamm und Gliedmassen), die sich innerhalb weniger Wochen bis Monate spontan zurückbilden. Allgemeinsymptome (Fieber, Gelenkschmerzen, Mattigkeit) können auftreten."},"es":{"name":"Mucinosis papular de resolución espontánea","definition":"La mucinosis papular de resolución espontánea es una forma poco frecuente de liquen mixedematoso localizado (consulte este término) que se da principalmente en niños y que se caracteriza por el desarrollo de pápulas mucinosas en varias partes del cuerpo (cara, cuello, tronco y extremidades) que se resuelven espontáneamente en algunas semanas o meses. Pueden observarse síntomas sistémicos como fiebre, artralgias y debilidad."},"it":{"name":"Mucinosi papulosa spontaneamente regressiva","definition":"La mucinosi papulosa spontaneamente regressiva è una forma rara del lichen mixedematoso localizzato (si veda questo termine), che interessa primariamente i bambini e si caratterizza per lo sviluppo di papule mucinose su diverse parti del corpo (faccia, collo, tronco e arti), che regrediscono spontaneamente entro qualche settimana-mese. Si possono associare alcuni sintomi, come la febbre, l'artralgia e la debolezza."},"nl":{"name":"Zelfhelende papulaire mucinose","definition":"Een zeldzame vorm van gelokaliseerde lichen myxoedematosus die vooral voorkomt bij kinderen, gekenmerkt door ontwikkeling van mucineuze papels op verschillende delen van het lichaam (aangezicht, hals, romp, en ledematen) die spontaan verdwijnen binnen enkele weken tot maanden. Systemische symptomen worden mogelijk ook waargenomen, zoals koorts, artralgie en zwakte."},"pt":{"name":"Mucinose papular autolimitada"},"pl":{"name":"Samowyleczalna mucynoza grudkowa"},"cs":{"name":"Self-healing papulární mucinóza"},"uk":{"name":"Самовиліковний папульозний муциноз","definition":"Self-healing papular mucinosis is a rare form of localized lichen myxedematosus (see this term) occurring primarily in children and characterized by the development of mucinous papules on various parts of the body (face, neck, trunk, and limbs) that resolve spontaneously within some weeks to months. Systemic symptoms can be observed such as fever, arthralgias and weakness."},"zh":{"name":"自愈性丘疹性粘蛋白沉积症"},"tr":{"name":"Kendi kendini iyileştiren papüler müsinoz"}},"xrefs":[{"source":"ICD-10","code":"L98.5","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"EB90.1Y","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"152781398"},{"source":"MONDO","code":"0019582","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0406657","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":86795,"name":"Localized lichen myxedematosus","classifications":[187]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":["All ages"],"prevalence":[{"type":"Cases/families","qualification":"Case(s)","class":null,"value":24.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"},{"type":"Point prevalence","qualification":"Class only","class":"<1 / 1 000 000","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"}],"phenotypes":null}