Langerhans cell histiocytosis in adults: literature review-Reference-Cited by-同舟云学术

Langerhans cell histiocytosis in adults: literature review

Published:2022-11-03 Issue:4 Volume:17 Page:16-32
ISSN:2413-4023
Container-title:Oncohematology
language:
Short-container-title:Onkogematologiâ

Author:

Potapenko V. G.¹^ORCID,Baykov V. V.²^ORCID,Zinchenko A. V.²^ORCID,Potikhonova N. A.³

Affiliation:

1. City Clinical Hospital No. 31

2. I.P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia

3. Russian Research Institute of Hematology and Transfusiology, Federal Medical and Biological Agency

Abstract

Langerhans cells histiocytosis is a variant of malignant histiocytosis. The course and symptoms vary. patients with localized forms have a better prognosis, because local therapy is effective. patients with multifocal forms of histiocytosis receive systemic drug therapy, which cures some of the patients. This review provides up-to-date data about typical presentation of the organ involvement, diagnosis, course and therapy of various forms of Langerhans cells histiocytosis.

Publisher

Publishing House ABV Press

Subject

Oncology,Hematology

Reference146 articles.

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2. Howarth D.M., Gilchrist G.S., Mullan B.P. et al. Langerhans cell histiocytosis: diagnosis, natural history, management, and outcome. Cancer 1999;(85):2278–90. DOI: 10.1002/(sici)10970142(19990515)85:10<2278::aidcncr25>3.0.co;2u

3. Goyal G., Shah M.V., Hook C.C. et al. Adult disseminated Langerhans cell histiocytosis: incidence, racial disparities and longterm outcomes. Br J Haematol 2018;182(4):579–81. DOI: 10.1111/bjh.14818

4. Campo E., Harris N.L., Pileri S.A. et al. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. Lyon, France: International Agency for Research on Cancer, 2017.

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