Conjunctival langerhans cell histiocytosis: a case report / 中国医学科学杂志(英文版)
Chinese Medical Sciences Journal
; (4): 63-64, 2015.
Article
in English
| WPRIM (Western Pacific)
| ID: wpr-242845
Responsible library:
WPRO
ABSTRACT
Langerhans cell histiocytosis (LCH) is a rare disease, mainly involving the bone, skin, lung, liver, spleen, and skin.1 The heterogenenous nature of LCH makes it difficult to diagnose. Not only do the involved organs vary from case to case, but also its natural history. Herein, we describe a rare case of conjuctival LCH in an Asian woman.
Full text:
Available
Database:
WPRIM (Western Pacific)
Main subject:
Prednisone
/
Histiocytosis, Langerhans-Cell
/
Cyclosporine
/
Conjunctival Diseases
/
Cyclophosphamide
/
Therapeutic Uses
/
Diagnosis
/
Drug Therapy
Type of study:
Diagnostic study
Limits:
Female
/
Humans
Language:
English
Journal:
Chinese Medical Sciences Journal
Year:
2015
Document type:
Article