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Cutaneous manifestations in patients with mastocytosis: Consensus report of the European Competence Network on Mastocytosis; the American Academy of Allergy, Asthma & Immunology; and the European Academy of Allergology and Clinical Immunology

Date
2016
Author
Oude Elberink, Joanna N. G.
Lange, Magdalena
Niedoszytko, Marek
Castells, Mariana
Bonadonna, Patrizia
Zanotti, Roberta
Hornick, Jason L.
Torrelo, Antonio
Grabbe, Juergen
Rabenhorst, Anja
Nedoszytko, Boguslaw
Butterfield, Joseph H.
Gotlib, Jason
Reiter, Andreas
Radia, Deepti
Hermine, Olivier
Sotlar, Karl
George, Tracy I.
Kristensen, Thomas K.
Kluin-Nelemans, Hanneke C.
Hagglund, Hans
Sperr, Wolfgang R.
Schwartz, Lawrence B.
Triggiani, Massimo
Maurer, Marcus
Nilsson, Gunnar
Horny, Hans-Peter
Arock, Michel
Orfao, Alberto
Metcalfe, Dean D.
Akin, Cem
Valent, Peter
Yavuz, Selim
Hartmann, Karin
Escribano, Luis
Grattan, Clive
Brockow, Knut
Carter, Melody C.
Alvarez-Twose, Ivan
Matito, Almudena
Broesby-Olsen, Sigurd
Siebenhaar, Frank
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Abstract
Cutaneous lesions in patients with mastocytosis are highly heterogeneous and encompass localized and disseminated forms. Although a classification and criteria for cutaneous mastocytosis (CM) have been proposed, there remains a need to better define subforms of cutaneous manifestations in patients with mastocytosis. To address this unmet need, an international task force involving experts from different organizations (including the European Competence Network on Mastocytosis; the American Academy of Allergy, Asthma & Immunology; and the European Academy of Allergology and Clinical Immunology) met several times between 2010 and 2014 to discuss the classification and criteria for diagnosis of cutaneous manifestations in patients with mastocytosis. This article provides the major outcomes of these meetings and a proposal for a revised definition and criteria. In particular, we recommend that the typical maculopapular cutaneous lesions (urticaria pigmentosa) should be subdivided into 2 variants, namely a monomorphic variant with small maculopapular lesions, which is typically seen in adult patients, and a polymorphic variant with larger lesions of variable size and shape, which is typically seen in pediatric patients. Clinical observations suggest that the monomorphic variant, if it develops in children, often persists into adulthood, whereas the polymorphic variant may resolve around puberty. This delineationmight have important prognostic implications, and its implementation in diagnostic algorithms and future mastocytosis classifications is recommended. Refinements are also suggested for the diagnostic criteria of CM, removal of telangiectasia macularis eruptiva perstans from the current classification of CM, and removal of the adjunct solitary from the term solitary mastocytoma.
URI
http://hdl.handle.net/20.500.12627/147836
https://doi.org/10.1016/j.jaci.2015.08.034
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Creative Commons Lisansı

İstanbul Üniversitesi Akademik Arşiv Sistemi (ilgili içerikte aksi belirtilmediği sürece) Creative Commons Alıntı-GayriTicari-Türetilemez 4.0 Uluslararası Lisansı ile lisanslanmıştır.

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