z-logo
open-access-imgOpen Access
Nadir bir hastalık; spontan pnömotoraks ile başvuran Erdheim-Chester hastalığı
Author(s) -
Mustafa Buğra Coşkuner,
Tevfik Özlü,
Yılmaz Bülbül
Publication year - 2019
Publication title -
tuberkuloz ve toraks/tüberküloz ve toraks
Language(s) - Turkish
Resource type - Journals
SCImago Journal Rank - 0.157
H-Index - 18
ISSN - 0494-1373
DOI - 10.5578/tt.68541
Subject(s) - erdheim–chester disease , histiocyte , histiocytosis , medicine , cd68 , pathology , etiology , infiltration (hvac) , disease , immunohistochemistry , physics , thermodynamics
Erdheim-Chester disease (ECD) is a rare non-Langerhans histiocytosis of unknown etiology, it is characterized by organ infiltration of foamy histiocytes. Diagnosis of ECD involves the analysis of histiocytes in tissue biopsies: these are typically CD68+ CD1a-. These characteristic histiocytes may be found in almost any tissue in cases of ECD. We present an interesting case of ECD that was presented by spontaneous pneumothorax and neurological involvement.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here