Langerhans cell histiocytosis in children with nasal congestion as chief complain: a case report.
- Author:
Yuanding ZHANG
;
Weilun CHEN
;
Yining LI
- Publication Type:Case Reports
- MeSH:
Histiocytosis, Langerhans-Cell;
diagnosis;
Humans;
Infant;
Rare Diseases
- From:
Journal of Clinical Otorhinolaryngology Head and Neck Surgery
2015;29(24):2177-2179
- CountryChina
- Language:Chinese
-
Abstract:
Langerhans cell histiocytosis (LCH) is a rare histiocytic disorder. Here, we report a rare case of multi-system LCH in a 20-month-old children presenting nasal congestion, fever, abnormal liver function, anemia, and skin damage. The radiograph computed tomography showed an osteolytic lesion in the lateral skull base with tumor extension. Pathological biopsy was performed, and the histopathologic diagnosis was LCH. A general review of LCH, including clinical manifestations, diagnosis, treatment, and prgognosis, is presented.
