Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753055 | PMC |
http://dx.doi.org/10.1016/j.jdcr.2021.11.024 | DOI Listing |
Front Med (Lausanne)
July 2024
The Intervention Center, Division of Technology and Innovation, Oslo University Hospital, Oslo, Norway.
Langerhans cell histiocytosis (LCH) is a complex disorder characterized by the clonal proliferation of Langerhans cells, primarily affecting children and adolescents. This condition exhibits a wide spectrum of clinical presentations, necessitating a multidisciplinary approach for diagnosis, treatment, and follow-up. Cutaneous manifestations of LCH are significant, mimicking common dermatoses and posing diagnostic challenges.
View Article and Find Full Text PDFJAAD Case Rep
December 2023
Department of Dermatology, University of Michigan, Ann Arbor, Michigan.
JAAD Case Rep
February 2022
Department of Dermatology, Yale University School of Medicine, New Haven, Connecticut.
Histopathology
January 2022
Department of Pathology, Ambroise Paré Hospital, AP-HP, Boulogne, France.
Case Rep Oncol Med
March 2021
Department of Radiation Medicine, Roswell Park Comprehensive Cancer Center, USA.
Langerhans cell histiocytosis (LCH) is a rare disease, afflicting approximately 4.6 and 1-2 per 1 million children and adults, respectively. While LCH can involve numerous organ systems such as the lung or bone, it is uncommon for the disease to be limited to the skin.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!