Thoracic amyloidomas: Two case reports of an evasive diagnosis
- PMID: 25057399
- PMCID: PMC4100224
- DOI: 10.1177/2054270414527280
Thoracic amyloidomas: Two case reports of an evasive diagnosis
Abstract
Amyloidosis is a rare differential diagnosis of a mass detected in the chest. Amyloidoma is caused by a local proliferation of clonal B-cells secreting an unstable immunoglobulin light chain which accumulates. FDG-PET scan are useful but not specific. Treatment is generally by local resection for treatment of symptoms. We report two cases of amyloidomas, which are rare entities characterised by large local amyloid deposits. These can occur in the upper respiratory tract, soft tissues and central nervous system.(1.)
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References
-
- Desai RA, Mahajan VK, Benjamin S, Van Ordstrand HS, Cordasco EM. Pulmonary amyloidoma and hilar adenopathy. Rare manifestations of primary amyloidosis. Chest 1979; 76: 170–173 - PubMed
-
- Bennhold H. Specific staining of amyloid by Congo Red [in German]. Münchener Medizinische Wochenschrift 1922; 69: 1537–1538
-
- Gertz M, Comenzo R, Falk R, Fermand JP, Hazenberg BP, Hawkins PN, et al. Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis, Tours, France, 18–22 April 2004. Am J Hematol 2005; 79: 319–328 - PubMed
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