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Sarcoidosis and multiple myeloma: Concurrent presentation of an unusual association
Literature on concurrent association of sarcoidosis with lymphoproliferative malignancies other than lymphoma e.g. multiple myeloma is meager. The rarity of the situation prompted us to report this patient who was a 51-year-old woman with a 2-years history of breathlessness, cough with expectoration...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748671/ https://www.ncbi.nlm.nih.gov/pubmed/26933313 http://dx.doi.org/10.4103/0970-2113.173068 |
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author | Nair, Vidya Prajapat, Deepak Talwar, Deepak |
author_facet | Nair, Vidya Prajapat, Deepak Talwar, Deepak |
author_sort | Nair, Vidya |
collection | PubMed |
description | Literature on concurrent association of sarcoidosis with lymphoproliferative malignancies other than lymphoma e.g. multiple myeloma is meager. The rarity of the situation prompted us to report this patient who was a 51-year-old woman with a 2-years history of breathlessness, cough with expectoration, chest pain and backache. Initial evaluation revealed mild anemia, increased alkaline phosphatase with chest skiagram showing both lower zone non homogenous opacities with calcified hilar lymph nodes. CECT chest showed mediastinal with bilateral hilar lymphadenopathy, parenchymal fibrosis, traction bronchiectasis, ground glass opacities, septal and peribronchovascular thickening affecting mid and lower lung zones bilaterally. MRI Dorsolumbar spine was suggestive of marrow infiltrative disorder. EBUS FNA of intrathoracic nodes, EBB and TBLB confirmed sarcoidosis. PET CT revealed hyper metabolic activity in lung, multiple lymph nodes and lytic bone lesions. Serum protein electrophoresis and immunofixation revealed a monoclonal paraprotein, immunoglobulin IgG kappa type. Bone marrow biopsy revealed an increase in plasma cells (15%), but no granulomas. Diagnosis of Indolent or multiple myeloma with sarcoidosis was established. 12 cases of sarcoidosis and multiple myeloma have been reported in literature, and mostly preceding the onset of multiple myeloma by many years, in our case both were diagnosed concurrently. |
format | Online Article Text |
id | pubmed-4748671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47486712016-03-01 Sarcoidosis and multiple myeloma: Concurrent presentation of an unusual association Nair, Vidya Prajapat, Deepak Talwar, Deepak Lung India Case Report Literature on concurrent association of sarcoidosis with lymphoproliferative malignancies other than lymphoma e.g. multiple myeloma is meager. The rarity of the situation prompted us to report this patient who was a 51-year-old woman with a 2-years history of breathlessness, cough with expectoration, chest pain and backache. Initial evaluation revealed mild anemia, increased alkaline phosphatase with chest skiagram showing both lower zone non homogenous opacities with calcified hilar lymph nodes. CECT chest showed mediastinal with bilateral hilar lymphadenopathy, parenchymal fibrosis, traction bronchiectasis, ground glass opacities, septal and peribronchovascular thickening affecting mid and lower lung zones bilaterally. MRI Dorsolumbar spine was suggestive of marrow infiltrative disorder. EBUS FNA of intrathoracic nodes, EBB and TBLB confirmed sarcoidosis. PET CT revealed hyper metabolic activity in lung, multiple lymph nodes and lytic bone lesions. Serum protein electrophoresis and immunofixation revealed a monoclonal paraprotein, immunoglobulin IgG kappa type. Bone marrow biopsy revealed an increase in plasma cells (15%), but no granulomas. Diagnosis of Indolent or multiple myeloma with sarcoidosis was established. 12 cases of sarcoidosis and multiple myeloma have been reported in literature, and mostly preceding the onset of multiple myeloma by many years, in our case both were diagnosed concurrently. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4748671/ /pubmed/26933313 http://dx.doi.org/10.4103/0970-2113.173068 Text en Copyright: © Lung India http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Nair, Vidya Prajapat, Deepak Talwar, Deepak Sarcoidosis and multiple myeloma: Concurrent presentation of an unusual association |
title | Sarcoidosis and multiple myeloma: Concurrent presentation of an unusual association |
title_full | Sarcoidosis and multiple myeloma: Concurrent presentation of an unusual association |
title_fullStr | Sarcoidosis and multiple myeloma: Concurrent presentation of an unusual association |
title_full_unstemmed | Sarcoidosis and multiple myeloma: Concurrent presentation of an unusual association |
title_short | Sarcoidosis and multiple myeloma: Concurrent presentation of an unusual association |
title_sort | sarcoidosis and multiple myeloma: concurrent presentation of an unusual association |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748671/ https://www.ncbi.nlm.nih.gov/pubmed/26933313 http://dx.doi.org/10.4103/0970-2113.173068 |
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