A case of thymic Langerhans cell histiocytosis with diabetes insipidus as the first presentation.

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 Med

journal_title

Frontiers of medicine

authors

Chen X,Huang X,Qiu Y,Chen H,Fu Y,Li X

doi

10.1007/s11684-013-0238-6

subject

Has Abstract

pub_date

2013-03-01 00:00:00

pages

143-6

issue

1

eissn

2095-0217

issn

2095-0225

journal_volume

7

pub_type

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