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Unisystem Langerhans cell histiocytosis in maxillofacial region in pediatrics: comprehensive and systematic review

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Abstract

Background

The study aimed to identify, enlist, and analyze cases of unisystem LCH in the maxillofacial pediatric population to understand the clinical presentation and encourage the consideration of this rare disease in the differential diagnosis. Langerhans cell histiocytosis (LCH) is an aggressive benign condition affecting mainly the pediatric population. It can be easily masked as periodontal disease in the maxillofacial region. Early diagnosis and a systemic evaluation are of utmost importance.

Methodology

We are presenting a complete review of literature in the pediatric population according to PRISMA guidelines for clinicopathologic, histopathological, immunohistochemistry, and treatment for unisystem LCH. The risk of bias assessment across studies was done using a Case series appraisal checklist by Guo et al. 53

Results

Forty-nine articles (152 cases) were selected which met our inclusion and exclusion criteria to be included in our review. Most of the patients fall in 6–12 years of age with the involvement of the mandibular body region in 40.79% cases. This disease mainly presents as erythematous gingiva, pain, swelling, and mobile teeth. Management can range from minimal intervention to chemotherapy and surgery.

Conclusion and practical implications

Although this is a rare condition, it should be considered especially in the pediatric population with periodontitis type lesions and floating teeth and comprehensive management should be followed. Early diagnosis of the disease is very important.

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Acknowledgements

We offer our sincere thanks to Dr. Daisy, Additional Professor, Pediatrics, for doing a systemic examination of the patients. We would also like to thank our patients for letting us use their photographs in the contribution of the scientific literature.

Why is this paper important?

  • As this disease mimics periodontitis, the dentist needs to keep this entity as one of the differential diagnosis in cases of extensive periodontitis.

  • Oral-cavity LCH can be a precursor to systemic LCH and systemic or multisystem LCH which has a poorer prognosis, knowing this disease can help in early diagnosis of its any severe form [79].

  • As most child dental problems are addressed by pediatric dentists, if they are versed with a broader picture, misdiagnosis or delayed diagnosis can be avoided.

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Correspondence to Amanjot Kaur.

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All procedures performed in the participants were according to the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

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This is a systematic review and Institutional Ethical Clearance was not required for this study. However, consent was taken from both patients for release of their photographs.

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Informed consent was obtained from both participants included in the study.

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The authors declare no competing interests.

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Chugh, A., Kaur, A., Kumar Patnana, A. et al. Unisystem Langerhans cell histiocytosis in maxillofacial region in pediatrics: comprehensive and systematic review. Oral Maxillofac Surg 25, 429–444 (2021). https://doi.org/10.1007/s10006-021-00949-9

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