Malignant Myeloma in a Patient after Treatment for Osteoporosis with Teriparatide; a Rare Coincidence
A breakthrough in understanding of mechanisms of bone structure regulation has brought about the introduction of the new synthetic recombinant human parathyroid hormone 1–34 (PTH1-34; Teriparatide) in the treatment of osteoporosis. These mechanisms, involving the RANKL, RANK, and osteoprotegerin sys...
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2008-01-01
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doaj-100a5de809c0407483c25b1a785f67c02020-11-25T03:27:19ZengSAGE PublishingClinical Medicine Insights: Case Reports1179-54762008-01-01110.4137/CCRep.S1026Malignant Myeloma in a Patient after Treatment for Osteoporosis with Teriparatide; a Rare CoincidenceTerje Forslund0Anna-Mari Koski1Arvo Koistinen2Anu Sikiö3Division of Nephrology, Department of Medicine, Central Finland Health Care District Hospital, Jyväskylä, Finland.Division of Endocrinology, Department of Medicine, Central Finland Health Care District Hospital, Jyväskylä, Finland.Division of Nephrology, Department of Medicine, Central Finland Health Care District Hospital, Jyväskylä, Finland.Division of Haematology, Department of Medicine, Central Finland Health Care District Hospital, Jyväskylä, Finland.A breakthrough in understanding of mechanisms of bone structure regulation has brought about the introduction of the new synthetic recombinant human parathyroid hormone 1–34 (PTH1-34; Teriparatide) in the treatment of osteoporosis. These mechanisms, involving the RANKL, RANK, and osteoprotegerin system, are also known to be involved in malignant myeloma (MM) and tumor and bone metastasis development. We report a case in which MM was found after treatment of osteoporosis with teriparatide. We were unable to demonstrate any direct association between the MM and teriparatide treatment. However, it seemed intriguing that similar mechanisms are activated in the development of MM as those being working during teriparatide treatment. In the view of our case, we propose that MM by examination of serum protein fraction should be searched for prior to treatment with teriparatide as it is an exclusion criterion in teriparatide treatment of secondary osteoporosis. A search for other metastatic diseases prior to teriparatide treatment should eventually also be considered. The theoretical basis for our proposal is discussed.https://doi.org/10.4137/CCRep.S1026 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Terje Forslund Anna-Mari Koski Arvo Koistinen Anu Sikiö |
spellingShingle |
Terje Forslund Anna-Mari Koski Arvo Koistinen Anu Sikiö Malignant Myeloma in a Patient after Treatment for Osteoporosis with Teriparatide; a Rare Coincidence Clinical Medicine Insights: Case Reports |
author_facet |
Terje Forslund Anna-Mari Koski Arvo Koistinen Anu Sikiö |
author_sort |
Terje Forslund |
title |
Malignant Myeloma in a Patient after Treatment for Osteoporosis with Teriparatide; a Rare Coincidence |
title_short |
Malignant Myeloma in a Patient after Treatment for Osteoporosis with Teriparatide; a Rare Coincidence |
title_full |
Malignant Myeloma in a Patient after Treatment for Osteoporosis with Teriparatide; a Rare Coincidence |
title_fullStr |
Malignant Myeloma in a Patient after Treatment for Osteoporosis with Teriparatide; a Rare Coincidence |
title_full_unstemmed |
Malignant Myeloma in a Patient after Treatment for Osteoporosis with Teriparatide; a Rare Coincidence |
title_sort |
malignant myeloma in a patient after treatment for osteoporosis with teriparatide; a rare coincidence |
publisher |
SAGE Publishing |
series |
Clinical Medicine Insights: Case Reports |
issn |
1179-5476 |
publishDate |
2008-01-01 |
description |
A breakthrough in understanding of mechanisms of bone structure regulation has brought about the introduction of the new synthetic recombinant human parathyroid hormone 1–34 (PTH1-34; Teriparatide) in the treatment of osteoporosis. These mechanisms, involving the RANKL, RANK, and osteoprotegerin system, are also known to be involved in malignant myeloma (MM) and tumor and bone metastasis development. We report a case in which MM was found after treatment of osteoporosis with teriparatide. We were unable to demonstrate any direct association between the MM and teriparatide treatment. However, it seemed intriguing that similar mechanisms are activated in the development of MM as those being working during teriparatide treatment. In the view of our case, we propose that MM by examination of serum protein fraction should be searched for prior to treatment with teriparatide as it is an exclusion criterion in teriparatide treatment of secondary osteoporosis. A search for other metastatic diseases prior to teriparatide treatment should eventually also be considered. The theoretical basis for our proposal is discussed. |
url |
https://doi.org/10.4137/CCRep.S1026 |
work_keys_str_mv |
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