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  3. Langerhans cell histiocytosis as differential diagnosis of a mediastinal tumor

Langerhans cell histiocytosis as differential diagnosis of a mediastinal tumor

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DOI
10.7892/boris.27143
Publisher DOI
10.1016/j.ejcts.2007.12.026
PubMed ID
18243003
Abstract
We describe the case of a 55-year-old man who presented with parasternal swelling. The chest CT scan showed a large tumor of the chest wall infiltrating the subcutaneous tissue. To assume histologic diagnosis an open biopsy was performed. Between the myofibrils a coarse, white tumor with infiltrative growth was noted. Histopathologic examination revealed expanded atrophic skeletal muscle that was infiltrated by histiocytic cells. Numerous eosinophilic granulocytes and lymphocytes CD20 and CD3 positive could be detected and immunohistochemical staining was also positive for S-100 proteins and CD1a. Histologic findings were characteristic of Langerhans cell histiocytosis (LCH). To the best of our knowledge a LCH originating from the mediastinum in an adult as presented has not been previously described.
Date Issued
2008
Publication Type
Article
Language(s)
en
Author(s)
Fahrner, René
Hoksch, Beatrix  
Universitätsklinik für Thoraxchirurgie  
Gugger, Mathias  
Institut für Pathologie  
Schmid, Ralph  
Universitätsklinik für Thoraxchirurgie  
Additional Credits
Universitätsklinik für Thoraxchirurgie  
Institut für Pathologie  
Journal
European journal of cardio-thoracic surgery
Publisher
Elsevier Science B.V.
ISSN
1010-7940
ISBN
18243003
Access(Rights)
open.access
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