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Osteosclerotic Multiple Myeloma without POEMS Syndrome – A Rare Case Report
INTRODUCTION: Multiple myeloma is a plasma cell neoplasm that is commonly associated with lytic bone lesions; however, osteosclerotic multiple myeloma is a rare entity. Osteosclerotic multiple myeloma has been reported in association with POEMS syndrome. CASE PRESENTATION: A 60-year-old female patie...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Indian Orthopaedic Research Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091408/ https://www.ncbi.nlm.nih.gov/pubmed/35611283 http://dx.doi.org/10.13107/jocr.2022.v12.i01.2598 |
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author | Divakar, M Shyam, Ashok Hadgaonkar, Shailesh Sancheti, Parag Aiyer, Siddharth N |
author_facet | Divakar, M Shyam, Ashok Hadgaonkar, Shailesh Sancheti, Parag Aiyer, Siddharth N |
author_sort | Divakar, M |
collection | PubMed |
description | INTRODUCTION: Multiple myeloma is a plasma cell neoplasm that is commonly associated with lytic bone lesions; however, osteosclerotic multiple myeloma is a rare entity. Osteosclerotic multiple myeloma has been reported in association with POEMS syndrome. CASE PRESENTATION: A 60-year-old female patient presented to us with low back pain for 2 months. The investigations revealed that the patient had multiple osteosclerotic lesions in the axial skeleton with a L4 ivory vertebra. The serum immunoelectrophoresis was negative. Positron emission tomography scan was done which showed multiple skeletal lesions in the right iliac bone, left femoral neck, thoracic vertebrae T1, T6, T12, and lumbar vertebra L4. Biopsy and immunohistochemistry of the lesion showed plasma cell proliferation; producing lambda light chains. However, there were no features of POEMS syndrome including polyneuropathy, organomegaly, endocrinopathy, and skin changes. The patient was started on chemoradiation and achieved clinical remission and was asymptomatic at 12 months follow-up. CONCLUSION: Osteosclerotic myeloma without the features of POEMS syndrome is an extremely rare entity. This case reports documents a unique clinical scenario of osteosclerotic non-secretory light chain myeloma without POEMS syndrome. |
format | Online Article Text |
id | pubmed-9091408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Indian Orthopaedic Research Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-90914082022-05-23 Osteosclerotic Multiple Myeloma without POEMS Syndrome – A Rare Case Report Divakar, M Shyam, Ashok Hadgaonkar, Shailesh Sancheti, Parag Aiyer, Siddharth N J Orthop Case Rep Case Report INTRODUCTION: Multiple myeloma is a plasma cell neoplasm that is commonly associated with lytic bone lesions; however, osteosclerotic multiple myeloma is a rare entity. Osteosclerotic multiple myeloma has been reported in association with POEMS syndrome. CASE PRESENTATION: A 60-year-old female patient presented to us with low back pain for 2 months. The investigations revealed that the patient had multiple osteosclerotic lesions in the axial skeleton with a L4 ivory vertebra. The serum immunoelectrophoresis was negative. Positron emission tomography scan was done which showed multiple skeletal lesions in the right iliac bone, left femoral neck, thoracic vertebrae T1, T6, T12, and lumbar vertebra L4. Biopsy and immunohistochemistry of the lesion showed plasma cell proliferation; producing lambda light chains. However, there were no features of POEMS syndrome including polyneuropathy, organomegaly, endocrinopathy, and skin changes. The patient was started on chemoradiation and achieved clinical remission and was asymptomatic at 12 months follow-up. CONCLUSION: Osteosclerotic myeloma without the features of POEMS syndrome is an extremely rare entity. This case reports documents a unique clinical scenario of osteosclerotic non-secretory light chain myeloma without POEMS syndrome. Indian Orthopaedic Research Group 2022-01 2022-01 /pmc/articles/PMC9091408/ /pubmed/35611283 http://dx.doi.org/10.13107/jocr.2022.v12.i01.2598 Text en Copyright: © Indian Orthopaedic Research Group https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Divakar, M Shyam, Ashok Hadgaonkar, Shailesh Sancheti, Parag Aiyer, Siddharth N Osteosclerotic Multiple Myeloma without POEMS Syndrome – A Rare Case Report |
title | Osteosclerotic Multiple Myeloma without POEMS Syndrome – A Rare Case Report |
title_full | Osteosclerotic Multiple Myeloma without POEMS Syndrome – A Rare Case Report |
title_fullStr | Osteosclerotic Multiple Myeloma without POEMS Syndrome – A Rare Case Report |
title_full_unstemmed | Osteosclerotic Multiple Myeloma without POEMS Syndrome – A Rare Case Report |
title_short | Osteosclerotic Multiple Myeloma without POEMS Syndrome – A Rare Case Report |
title_sort | osteosclerotic multiple myeloma without poems syndrome – a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091408/ https://www.ncbi.nlm.nih.gov/pubmed/35611283 http://dx.doi.org/10.13107/jocr.2022.v12.i01.2598 |
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