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Proposed diagnostic algorithm for patients with suspected mastocytosis: a proposal of the European Competence Network on Mastocytosis

Authors :
Knut Brockow
Cem Akin
Jason Gotlib
Peter Valent
H.-P. Horny
Thomas Kielsgaard Kristensen
Hanneke C. Kluin-Nelemans
J. J. Van Doormaal
Joseph H. Butterfield
Karin Hartmann
Lawrence B. Schwartz
Clive Grattan
Olivier Hermine
Bogusław Nedoszytko
Andreas Reiter
Dean D. Metcalfe
Marek Niedoszytko
Karl Sotlar
Iván Álvarez-Twose
Wolfgang R. Sperr
J. N. G. Oude Elberink
Michel Arock
Massimo Triggiani
Marcus Maurer
Mariana Castells
Luis Escribano
A. Orfao
Selim Yavuz
Deepti Radia
Sigurd Broesby-Olsen
Frank Siebenhaar
Austrian Science Fund
National Institute of Allergy and Infectious Diseases (US)
Source :
Digital.CSIC. Repositorio Institucional del CSIC, instname, Valent, P, Escribano, L, Broesby-Olsen, S, Hartmann, K, Grattan, C, Brockow, K, Niedoszytko, M, Nedoszytko, B, Oude Elberink, J N G, Kielsgaard Kristensen, T, Butterfield, J H, Triggiani, M, Alvarez-Twose, I, Reiter, A, Sperr, W R, Sotlar, K, Yavuz, S, Kluin-Nelemans, H C, Hermine, O, Radia, D, van Doormaal, J J, Gotlib, J, Orfao, A, Siebenhaar, F, Schwartz, L B, Castells, M, Maurer, M, Horny, H-P, Akin, C, Metcalfe, D D & Arock, M 2014, ' Proposed diagnostic algorithm for patients with suspected mastocytosis : a proposal of the European Competence Network on Mastocytosis ', Allergy: European Journal of Allergy and Clinical Immunology, vol. 69, no. 10, pp. 1267-1274 . https://doi.org/10.1111/all.12436
Publication Year :
2014
Publisher :
Wiley, 2014.

Abstract

Mastocytosis is an emerging differential diagnosis in patients with more or less specific mediator-related symptoms. In some of these patients, typical skin lesions are found and the diagnosis of mastocytosis can be established. In other cases, however, skin lesions are absent, which represents a diagnostic challenge. In the light of this unmet need, we developed a diagnostic algorithm for patients with suspected mastocytosis. In adult patients with typical lesions of mastocytosis in the skin, a bone marrow (BM) biopsy should be considered, regardless of the basal serum tryptase concentration. In adults without skin lesions who suffer from mediator-related or other typical symptoms, the basal tryptase level is an important parameter. In those with a slightly increased tryptase level, additional investigations, including a sensitive KIT mutation analysis of blood leucocytes or measurement of urinary histamine metabolites, may be helpful. In adult patients in whom (i) KIT D816V is detected and/or (ii) the basal serum tryptase level is clearly increased (>25-30 ng/ ml) and/or (iii) other clinical or laboratory features suggest the presence of 'occult' mastocytosis or another haematologic neoplasm, a BM investigation is recommended. In the absence of KIT D816V and other signs or symptoms of mastocytosis or another haematopoietic disease, no BM investigation is required, but the clinical course and tryptase levels are monitored in the follow-up. In paediatric patients, a BM investigation is usually not required, even if the tryptase level is increased. Although validation is required, it can be expected that the algorithm proposed herein will facilitate the management of patients with suspected mastocytosis and help avoid unnecessary referrals and investigations.<br />This work was supported in part by the Austrian Science Funds (FWF) Project SFB F4611 and SFB F4704-B20 and the Division of Intramural Research, NIAID.

Details

ISSN :
01054538
Volume :
69
Database :
OpenAIRE
Journal :
Allergy
Accession number :
edsair.doi.dedup.....10850f9124542b6c8cf2820e0210eed9
Full Text :
https://doi.org/10.1111/all.12436