Literature DB >> 27514589

Langerhans Cell Histiocytosis and Other Histiocytic Diseases of the Lung.

Erin DeMartino1, Ronald S Go2, Robert Vassallo3.   

Abstract

Several histiocytic disorders may affect the thoracic cavity. Pulmonary Langerhans cell histiocytosis (LCH) is the histiocytic disorder that most frequently manifests with thoracic involvement in adults and is associated with cigarette smoking. The histiocytic disorders follow variable clinical courses ranging from benign disease to life-threatening aggressive disorders. Although the pathogenesis is not fully understood, it is now apparent that some of these disorders are associated with activating mutations in cell proliferative/regulatory pathways. Management of these rare disorders must be individualized. Pharmacologic treatment may include the use of chemotherapeutic agents. Smoking cessation is imperative in the management of pulmonary LCH.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  BRAF; Cigarette smoking; Histiocyte; Interstitial; Langerhans cell; Lung; Macrophage

Mesh:

Substances:

Year:  2016        PMID: 27514589     DOI: 10.1016/j.ccm.2016.04.005

Source DB:  PubMed          Journal:  Clin Chest Med        ISSN: 0272-5231            Impact factor:   2.878


  3 in total

1.  Diffuse cystic lung diseases: differential diagnosis.

Authors:  Bruno Guedes Baldi; Carlos Roberto Ribeiro Carvalho; Olívia Meira Dias; Edson Marchiori; Bruno Hochhegger
Journal:  J Bras Pneumol       Date:  2017 Mar-Apr       Impact factor: 2.624

2.  Chronic cough and weight loss in an adolescent marijuana smoker.

Authors:  Angela Onorato; Jana Shapiro; Lindsay Griffin; Monica Aldulescu; Nicoleta C Arva; Avani Shah
Journal:  SAGE Open Med Case Rep       Date:  2022-03-22

3.  Progression of a rare multiple cystic lung disease.

Authors:  Kamal Gera; Ajay Lall; Ritu Kulshrestha; Kanika Singh; Nandini Chhabra
Journal:  Lung India       Date:  2017 Jul-Aug
  3 in total

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