Parallel occurrence of Erdheim–Chester disease and eosinophilic granuloma in the same patient
✍ Scribed by R Kerzl; Kilian Eyerich; B Eberlein; R Hein; I Weichenmeier; H Behrendt; C Clemm; F Fend; S Mempel; S Waldt; J Ring; M Mempel
- Book ID
- 111095636
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 834 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0926-9959
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## Abstract ## Objective Erdheim‐Chester disease (ECD) is a rare, non‐Langerhans form of histiocytosis of unknown origin, characterized by infiltration of tissues by spumous histiocytes. ECD features heterogeneous systemic manifestations, and the general prognosis remains poor despite various trea
## Abstract ## Objective Erdheim‐Chester disease (ECD) is a rare form of non–Langerhans' cell histiocytosis (LCH) of unknown etiology, characterized by diffuse histiocyte infiltration of bones and soft tissue. The purpose of this study was to assess cell proliferation and expression of cytokines,
## Abstract ## Objective Erdheim‐Chester disease (ECD) is a rare form of non–Langerhans' cell histiocytosis that may present with pulmonary involvement. We undertook the current study to evaluate the characteristic features of pulmonary involvement in ECD, in the largest single‐center series of pa
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