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Langerhans cell histiocytosis in children with nasal congestion as chief complain: a case report / 临床耳鼻咽喉头颈外科杂志
Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 2177-2179, 2015.
Article in Chinese | WPRIM | ID: wpr-746843
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.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Histiocytosis, Langerhans-Cell / Rare Diseases / Diagnosis Type of study: Diagnostic study Limits: Humans / Infant Language: Chinese Journal: Journal of Clinical Otorhinolaryngology Head and Neck Surgery Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Histiocytosis, Langerhans-Cell / Rare Diseases / Diagnosis Type of study: Diagnostic study Limits: Humans / Infant Language: Chinese Journal: Journal of Clinical Otorhinolaryngology Head and Neck Surgery Year: 2015 Type: Article