NHÂN TRƯỜNG HỢP U MÔ BÀO LANGERHANS HIẾM GẶP XƯƠNG HÀM DƯỚI

Dân Nguyễn Văn; Huệ Hoàng Lê; Nhân Trịnh Văn

doi:10.59354/ydth175.2024.293

Keywords:

Langerhans cell histiocytosis, mandibular

Abstract

Langerhans cell histiocytosis (LCH) is a rare disorder characterized by the proliferation of Langerhans cells. The clinical symptoms of patients with Langerhans cell histiocytosis depend on the site and the degree of involvement. The proportion of LCH in mandibular is reported from 10% to 20% of total LCH patients. LCH treating methods are various including the surgical curettage, the radiation therapy, the steroid injection, and the chemotherapy. LCH has a good prognosis. Regular follow-up must be performed even after healing.

We report the clinical case: a 42-year-old male patient was diagnosed with LCH in mandibular, treated with surgery and the steroid injection at hospital 175.

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