Abstract:
:Langerhans cell histiocytosis (LCH) is an idiopathic group of reactive proliferative diseases linked to aberrant immunity, pathologically characterized by clonal proliferation of Langerhans cells. LCH rarely involves the thymus. We report a case of thymic LCH with diabetes insipidus as the first presentation, without evidence of myasthenia gravis and without evidenced involvement of the skin, liver, spleen, bones, lungs and superficial lymph nodes. This present case may have important clinical implications. In screening for LCH lesions, attention should be attached to rarely involved sites in addition to commonly involved organs. Follow-up and imageological examination are very important to a final diagnosis.
journal_name
Front Medjournal_title
Frontiers of medicineauthors
Chen X,Huang X,Qiu Y,Chen H,Fu Y,Li Xdoi
10.1007/s11684-013-0238-6subject
Has Abstractpub_date
2013-03-01 00:00:00pages
143-6issue
1eissn
2095-0217issn
2095-0225journal_volume
7pub_type
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