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Progress in understanding the pathogenesis of Langerhans cell histiocytosis: back to Histiocytosis X?
Berres ML, Merad M, Allen CE. Berres ML, et al. Br J Haematol. 2015 Apr;169(1):3-13. doi: 10.1111/bjh.13247. Epub 2014 Nov 28. Br J Haematol. 2015. PMID: 25430560 Free PMC article. Review.
Langerhans cell histiocytosis (LCH), the most common histiocytic disorder, is characterized by the accumulation of CD1A(+) /CD207(+) mononuclear phagocytes within granulomatous lesions that can affect nearly all organ systems. Historically, LCH has been presu
Langerhans cell histiocytosis (LCH), the most common histiocytic disorder, is characterized by the accumulation of CD1A
Recurrence of a Langerhans Cell Histiocytosis bone lesion in a different site: A case report.
Al Abdulsalam A, Kapila K, Alherz M, Alsayegh M. Al Abdulsalam A, et al. Ann Med Surg (Lond). 2022 Feb 24;75:103401. doi: 10.1016/j.amsu.2022.103401. eCollection 2022 Mar. Ann Med Surg (Lond). 2022. PMID: 35242335 Free PMC article.
INTRODUCTION: Langerhans' Cell Histiocytosis is a rare disease of unknown etiology, the pathogenesis of which involves both reactive and neoplastic processes. ...CLINICAL DISCUSSION: There is a diverse array of documented presentations of …
INTRODUCTION: Langerhans' Cell Histiocytosis is a rare disease of unknown etiology, the pathogenesis