*Corresponding Author: Otto Alemán Miranda, General Clinical and Surgical Hospital Orlando Pantoja Tamayo, Cuba.

Received: May 17, 2024; Published: June 20, 2024

Abstract

Histiocytosis is a heterogeneous group of diseases of unknown cause that are characterized by the proliferation of cells of the mononuclear phagocytic system (MFS) (monocytes, macrophages, dendritic cells) in different organs and systems. Therefore, a bibliographic review was carried out on the lesions and risks in histocytic syndromes.

Keywords: Histiocytosis; Bone Resorption; Oral Manifestation; Syndrome

References

1. Cruz O and Astigarraga I. “Histiocitosis en la edad pediátrica. En: Tratado de Oncología Pediátrica, Luis Sierrasesúmaga Editor”. Prentice-Hall (Pearson Educacion) 417 (2002):
2. Gadner H., et al. “A randomized trial of treatment for multisystem Langerhans’ cell histiocytosis”. The Journal of Pediatrics 138 (2001): 728-734.
3. Hofmann M., et al. “Diffuse normolipemic plane xanthoma in a 9-year-old boy”. Pediatric Dermatology 22 (2005): 127-129.
4. Dehiner LP. “Juvenile xanthogranulomas in the first two decades of life: A clinipathologic study of 174 cases with cutaneous and extracutaneous manifestations”. The American Journal of Surgical Pathology 27 (2003): 579-593.
5. Gadner H., et al. “A randomized trial of treatment for multisystem Langerhans’ cell histiocytosis”. The Journal of Pediatrics 5 (2001).
6. Larroche C and Mouthon L. “Pathogenesis of hemophagocytic syndrome (HPS)”. Autoimmunity Reviews 2 (2004): 69-75.
7. Mitomi T., et al. “Tooth devehopment included in the multifocal jaw lesions of Langerhans cell histiocytosis”. International Journal of Paediatric Dentistry 2 (2005): 123-126.
8. Allen CE., et al. “Cell-specific gene expression in Langerhans cell histiocytosis lesions reveals a distinct profile compared with epidermal Langerhans cells”. The Journal of Immunology 8 (2010): 4557-4567.
9. Arceci RJ., et al. “Atypical cellular disorders”. Hematology American Society Hematology Education Program (2002): 297-314. 
10. Coppes-Zantinga A and Egeler RM. “The Langerhans cell histiocytosis X files revealed”. British Journal of Haematology 1 (2002): 3-9. 
11. Laman JD., et al. “Langerhans-cell histiocytosis 'insight into DC biology”. Trends in Immunology 4 (2009): 190-196. 
12. Schmitz L and Favara BE. “Nosology and pathology of Langerhans cell histiocytosis”. Hematology/Oncology Clinics of North America 12 (1998): 221-246.
13. Favara BE and Jaffe R. “Pathology of Langerhans cell histiocytes”. Hematology/Oncology Clinics of North America 1 (1987): 75-97.
14. “Histiocyte Society Writing Group. Histiocytosis syndrome in children”. Lancet 1 (1987): 208-209.
15. Thomas C., et al. “Groupe dÉtude sur l´Histiocytosis lanhergansienne de la Societé d´Hematologie et d´Inmunologie Pediatriques”. Archives de Pédiatrie 3 (1996): 63-69.
16. Favara BE., et al. “A contemporary clasification of histiocytic disorders of childhood”. Medical and Pediatric Oncology 29 (1997): 157-166.
17. Favara BE. “Langerhans cell histiocytosis: pathobiology and pathogenesis”. Seminars in Oncology 18 (1991): 3-7.
18. The French Langerhans cell histiocytosis study group: 348 cases observed between 1983 and 1993”. Archives of Disease in Childhood 75 (1996): 17-24
19. Kannouraris G and Abbas A. “The role of citokines in the pathogenesis of Langerhans cell histiocytosis”. British Journal of Cancer 70 (1994): s37-40.
20. Catersen H and Ornvold K. “The epidemiology of Langerhans cell histiocytosis in children in Denmark 1975-1984”. Medical and Pediatric Oncology 21 (1993): 387-388.
21. Graaf J., et al. “Expression of cellular adhesion molecules in Langerhans cell histiocytosis and normal Langerhans cell”. The American Journal of Pathology 147 (1995): 1161-1171.
22. Núñez Cambre., et al. “La gammagrafía ósea en el granuloma eosinófilo”. Servicio de Medicina Nuclear Hospital Clínico Universitario Santiago de Compostela 8 (2004).
23. C Jorge Santana Álvarez I., et al. “Histiocitosis X: presentación de tres casos”. Revista Archivo Médico de Camagüey6 (2010): 1025-0255.
24. Cervera JL., et al. “Histiocitosis de células de Langerhans del hueso temporal”. Radiología 45 (2003):
25. Pena Pardo FJ., et al. “Gammagrafía ósea en la enfermedad de Erdheim-Chester”. Revista Española de Medicina Nuclear 22 (2003): 253-256.
26. Lucioni M., et al. “Congenital aggressive variant of Langerhans cells histiocytosis with CD56+/E-Cadherin- phenotype”. Pediatric Blood and Cancer 2 (2009): 201-242.

Citation

Citation: Otto Alemán Miranda., et al. “Risks in Histiocytic Syndromes".Acta Scientific Dental Sciences 8.7 (2024): 54-59.

Copyright

Copyright: Otto Alemán Miranda., et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.