Literature DB >> 27721292

Soft-tissue amyloidoma with associated plasmacytoma.

Bibhas Saha Dalal1, Piyabi Sarkar1, Namrata Maity1, Sayed Mahmood Nadeem2.   

Abstract

Soft tissue amyloidoma with features similar to plasmacytoma, in absence of systemic amyloidosis, is an extremely rare finding. We hereby report the case of a 77 year old man who presented with a painless, nodular swelling on chest wall, diagnosed as soft tissue amyloidoma with plasma cell infiltration. Congo red staining was done to prove the presence of amyloid which showed characteristic "apple-green" birefringence on polarized microscopy. The plasma cells were monoclonal in origin as demonstrated by serum protein and immunofixation electrophoresis. To the best of our knowledge, this is the second such reported case. However close follow up is required, as this patient may develop multiple myeloma in future.

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Year:  2016        PMID: 27721292     DOI: 10.4103/0377-4929.191821

Source DB:  PubMed          Journal:  Indian J Pathol Microbiol        ISSN: 0377-4929            Impact factor:   0.740


  3 in total

Review 1.  Amyloidoma: a review and case report.

Authors:  Sohil S Desai; Michael G Rizzo; Augustus J Rush; Andrew E Rosenberg; Motasem Al Maaieh
Journal:  Skeletal Radiol       Date:  2020-07-24       Impact factor: 2.199

2.  A Rare Case of Amyloidoma of the Chest Wall Presented with Fever of Unknown Origin.

Authors:  Hsien-Po Huang; Shang-Feng Tsai
Journal:  Diagnostics (Basel)       Date:  2022-04-06

3.  Primary nodular chest amyloidoma: A case report and review of literature.

Authors:  Matthew A Crain; Georgia M Vasilakis; Jessica R Adkins; Ayodele Adelanwa; Jeffery P Hogg; Dhairya A Lakhani; Cathy Kim
Journal:  Radiol Case Rep       Date:  2021-12-21
  3 in total

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