Literature DB >> 22284564

Pulmonary involvement in pediatric-onset multisystem Langerhans cell histiocytosis: effect on course and outcome.

Leila Ronceray1, Ulrike Pötschger, Gritta Janka, Helmut Gadner, Milen Minkov.   

Abstract

OBJECTIVES: To assess the effect of pulmonary involvement on the course and outcome of multisystem Langerhans cell histiocytosis (MS-LCH) in children. STUDY
DESIGN: We conducted a retrospective analysis of 420 consecutive patients with MS-LCH. In this analysis, the term "risk organs" is defined as involvement of the liver, spleen, and/or hematopoietic system. The effect of pulmonary involvement on survival was assessed with multivariate Cox regression with adjustment for risk organs involvement and age.
RESULTS: Pulmonary involvement in MS-LCH was present at diagnosis in 102 patients (24%). Of the 318 patients without pulmonary involvement at diagnosis, it developed in 28 within a median of 10 months (range, 1 month-5.5 years). The 5-year overall survival rate in patients without risk organ involvement at diagnosis was 96% in patients without pulmonary involvement and 94% in those with pulmonary involvement. In patients with risk organ involvement at diagnosis, the 5-year overall survival rate was 73% in patients without pulmonary involvement and 65% in patients with pulmonary involvement. In multivariate analysis, pulmonary involvement at diagnosis had no significant impact on survival rats (P = .109, hazard ratio = 1.5).
CONCLUSIONS: In multivariate analysis, pulmonary involvement was not an independent prognostic variable and should therefore be excluded from the definition of risk organ involvement in MS-LCH.
Copyright © 2012 Mosby, Inc. All rights reserved.

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Year:  2012        PMID: 22284564     DOI: 10.1016/j.jpeds.2011.12.035

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  23 in total

1.  Differentiating skin-limited and multisystem Langerhans cell histiocytosis.

Authors:  Stephen J Simko; Benjamin Garmezy; Harshal Abhyankar; Philip J Lupo; Rikhia Chakraborty; Karen Phaik Har Lim; Albert Shih; M John Hicks; Teresa S Wright; Moise L Levy; Kenneth L McClain; Carl E Allen
Journal:  J Pediatr       Date:  2014-10-21       Impact factor: 4.406

2.  A case of invasive Langerhans cell histiocytosis localizing only in the lung and diagnosed as pneumothorax in an adolescent female.

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3.  [Clinical features and prognosis of Langerhans cell histiocytosis in children: an analysis of 34 cases].

Authors:  Dan Li; Hui Li; Hong Shi
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2017-06

Review 4.  Histiocytic disorders.

Authors:  Kenneth L McClain; Camille Bigenwald; Matthew Collin; Julien Haroche; Rebecca A Marsh; Miriam Merad; Jennifer Picarsic; Karina B Ribeiro; Carl E Allen
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Authors:  Stephen J Simko; Huy D Tran; Jeremy Jones; Mrinalini Bilgi; Lynda Kwon Beaupin; Don Coulter; Timothy Garrington; Timothy L McCavit; Colin Moore; Francisco Rivera-Ortegón; Linda Shaffer; Linda Stork; Lucie Turcotte; Esperanza C Welsh; M John Hicks; Kenneth L McClain; Carl E Allen
Journal:  Pediatr Blood Cancer       Date:  2013-09-18       Impact factor: 3.167

6.  Management of severe pulmonary Langerhans cell histiocytosis in children.

Authors:  Olive S Eckstein; Jed G Nuchtern; George B Mallory; R Paul Guillerman; Matthew A Musick; Mhairi Barclay; Jayesh M Bhatt; Patrick Davies; Richard G Grundy; Alice Martin; Tom Hilliard; Stephen P Lowis; Susan Picton; Vasanta Nanduri; Johannes Visser; Carl E Allen; Kenneth L McClain
Journal:  Pediatr Pulmonol       Date:  2020-06-08

7.  Intensified and prolonged therapy comprising cytarabine, vincristine and prednisolone improves outcome in patients with multisystem Langerhans cell histiocytosis: results of the Japan Langerhans Cell Histiocytosis Study Group-02 Protocol Study.

Authors:  Akira Morimoto; Yoko Shioda; Toshihiko Imamura; Kazuko Kudo; Hiroshi Kawaguchi; Kazuo Sakashita; Masahiro Yasui; Yuhki Koga; Ryoji Kobayashi; Eiichi Ishii; Junichiro Fujimoto; Keizo Horibe; Fumio Bessho; Yukiko Tsunematsu; Shinsaku Imashuku
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8.  Recurrent pulmonary infections as the first presentation of Letterer Siwe disease.

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Journal:  Oxf Med Case Reports       Date:  2021-07-21

9.  Acute-phase ITIH4 levels distinguish multi-system from single-system Langerhans cell histiocytosis via plasma peptidomics.

Authors:  Ichiro Murakami; Yukiko Oh; Akira Morimoto; Hitoshi Sano; Susumu Kanzaki; Michiko Matsushita; Takeshi Iwasaki; Satoshi Kuwamoto; Masako Kato; Keiko Nagata; Kazuhiko Hayashi; Shinsaku Imashuku; Jean Gogusev; Francis Jaubert; Takashi Oka; Tadashi Yoshino
Journal:  Clin Proteomics       Date:  2015-06-18       Impact factor: 3.988

10.  Langerhans cell histiocytosis (LCH): guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years.

Authors:  Riccardo Haupt; Milen Minkov; Itziar Astigarraga; Eva Schäfer; Vasanta Nanduri; Rima Jubran; R Maarten Egeler; Gritta Janka; Dragan Micic; Carlos Rodriguez-Galindo; Stefaan Van Gool; Johannes Visser; Sheila Weitzman; Jean Donadieu
Journal:  Pediatr Blood Cancer       Date:  2012-10-25       Impact factor: 3.167

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