Langerhans cell histiocytosis
نویسندگان
چکیده مقاله:
Introduction: Langerhans cell histiocytosis (LCH), which was previously known as histiocytosis X, refers to a group of lesions that stimulate uncontrolled proliferation of cells. The purpose of this case was to report and describe a LCH case with mandibular bone involvement in a 2.5-year-old boy. Case reports: A 2.5 years old boy with LCH of mandibular jaw who has been treated by surgical intervention and chemotherapy and followed more than two years. Conclusion: LCH of the mandible is a rare lesion of the langerhans cells which could be treated with early accurate diagnosis. Therefore, to reach the best response to treatment, early diagnosis based on recognition of clinical and radiographic features of the lesion is very important.
منابع مشابه
Current Treatment Strategy in Langerhans Cell Histiocytosis
Langerhans cell histiocytosis (LCH) is a rare disorder described as three different entities including eosinophilic granulomaof bone, the Hand-Schuller-Christian syndrome, and Letterer-Siwe disease. LCH is currently classified into singlesystem LCH, and multisystem LCH. Patients with single system LCH have an excellent prognosis, and are mostlytreated with local therapy. Multisystem LCH is subd...
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عنوان ژورنال
دوره 21 شماره 3
صفحات 576- 578
تاریخ انتشار 2019-06
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