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Xu, C. Langerhans Cell Histiocytosis. Encyclopedia. Available online: https://encyclopedia.pub/entry/4479 (accessed on 28 September 2026).
Xu C. Langerhans Cell Histiocytosis. Encyclopedia. Available at: https://encyclopedia.pub/entry/4479. Accessed September 28, 2026.
Xu, Camila. "Langerhans Cell Histiocytosis" Encyclopedia, https://encyclopedia.pub/entry/4479 (accessed September 28, 2026).
Xu, C. (2020, December 23). Langerhans Cell Histiocytosis. In Encyclopedia. https://encyclopedia.pub/entry/4479
Xu, Camila. "Langerhans Cell Histiocytosis." Encyclopedia. Web. 23 December, 2020.
Langerhans Cell Histiocytosis
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/langerhans-cell-histiocytosis

Langerhans cell histiocytosis is a disorder in which excess immune system cells called Langerhans cells build up in the body.

genetic conditions

References

  1. Allen CE, Parsons DW. Biological and clinical significance of somaticmutations in Langerhans cell histiocytosis and related histiocytic neoplasticdisorders. Hematology Am Soc Hematol Educ Program. 2015;2015:559-64. doi:10.1182/asheducation-2015.1.559. Review.
  2. Collin M, Bigley V, McClain KL, Allen CE. Cell(s) of Origin of Langerhans CellHistiocytosis. Hematol Oncol Clin North Am. 2015 Oct;29(5):825-38. doi:10.1016/j.hoc.2015.06.003.
  3. Egeler RM, Katewa S, Leenen PJ, Beverley P, Collin M, Ginhoux F, Arceci RJ,Rollins BJ; Steering Committee of the Nikolas Symposium. Langerhans cellhistiocytosis is a neoplasm and consequently its recurrence is a relapse: Inmemory of Bob Arceci. Pediatr Blood Cancer. 2016 Oct;63(10):1704-12. doi:10.1002/pbc.26104.
  4. El Demellawy D, Young JL, de Nanassy J, Chernetsova E, Nasr A. Langerhans cellhistiocytosis: a comprehensive review. Pathology. 2015 Jun;47(4):294-301. doi:10.1097/PAT.0000000000000256. Review.
  5. Grana N. Langerhans cell histiocytosis. Cancer Control. 2014 Oct;21(4):328-34.Review.
  6. Harmon CM, Brown N. Langerhans Cell Histiocytosis: A Clinicopathologic Review and Molecular Pathogenetic Update. Arch Pathol Lab Med. 2015 Oct;139(10):1211-4. doi: 10.5858/arpa.2015-0199-RA. Review.
  7. Monsereenusorn C, Rodriguez-Galindo C. Clinical Characteristics and Treatment of Langerhans Cell Histiocytosis. Hematol Oncol Clin North Am. 2015Oct;29(5):853-73. doi: 10.1016/j.hoc.2015.06.005.
  8. Nelson DS, van Halteren A, Quispel WT, van den Bos C, Bovée JV, Patel B,Badalian-Very G, van Hummelen P, Ducar M, Lin L, MacConaill LE, Egeler RM,Rollins BJ. MAP2K1 and MAP3K1 mutations in Langerhans cell histiocytosis. GenesChromosomes Cancer. 2015 Jun;54(6):361-8. doi: 10.1002/gcc.22247.
  9. Roden AC, Hu X, Kip S, Parrilla Castellar ER, Rumilla KM, Vrana JA, VassalloR, Ryu JH, Yi ES. BRAF V600E expression in Langerhans cell histiocytosis:clinical and immunohistochemical study on 25 pulmonary and 54 extrapulmonarycases. Am J Surg Pathol. 2014 Apr;38(4):548-51. doi:10.1097/PAS.0000000000000129.
  10. Rollins BJ. Genomic Alterations in Langerhans Cell Histiocytosis. HematolOncol Clin North Am. 2015 Oct;29(5):839-51. doi: 10.1016/j.hoc.2015.06.004.Review.
  11. Zinn DJ, Chakraborty R, Allen CE. Langerhans Cell Histiocytosis: EmergingInsights and Clinical Implications. Oncology (Williston Park). 2016Feb;30(2):122-32, 139. Review.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Camila Xu
View Times: 794
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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