16개월 유아에서 발생한 랑게르한스 세포 조직구증: 증례보고 및 임상적 조직학적 양상에 대한 고찰
Langerhans Cell Histiocytosis in a 16-month-old Child: Case Report and Review of Clinical & Histopathological Features
김도형, 최소형,
소속 상세정보
김도형 ( Kim Do-Hyoung ) -
최소형 ( Choi So-Young ) -
Abstract
Langerhans cell histiocytosis (LCH) is a rare disease that arises from an abnormal increase in histiocytes. Due to its rare occurrence, the diagnosis of LCH is often delayed or missed. This report presents a case of LCH in a 16-month-old girl. After biopsy, the patient’s previous medical records were obtained. The records described the presence of a yellowish plaque on the forehead since birth, a characteristic feature of LCH. Earlier knowledge of this medical history would have helped facilitate the diagnosis of LCH. This report aims to inform clinicians of the clinical and histopathological features of LCH in order to aid in the early diagnosis of this disease, which can occur in infancy.
키워드
Langerhans cell histiocytosis; Mandible; Child; Chemotherapy
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