Joint Pain and Arthritis as First Clinical Manifestation of Systemic Amyloidosis and Multiple Myeloma: Case Report and Brief Literature Review
Amyloidosis is a rare disease that is often seen in conjunction with multiple myeloma (MM). Its damage varies depending on the anatomical site affected; however, it is believed that many cases of amyloidosis are misrecognized due to the fact that its signs and symptoms are nonspecific. Joint amyloid...
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Published in | Hematology reports Vol. 14; no. 1; pp. 19 - 23 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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02.03.2022
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Abstract | Amyloidosis is a rare disease that is often seen in conjunction with multiple myeloma (MM). Its damage varies depending on the anatomical site affected; however, it is believed that many cases of amyloidosis are misrecognized due to the fact that its signs and symptoms are nonspecific. Joint amyloidosis, in particular, may be confused with degenerative or autoimmune diseases. When it is associated with MM, it can significantly precede the diagnosis of the latter. We describe a case report of a woman of Nigerian heritage diagnosed with MM with widespread joint manifestations compatible with a diagnosis of amyloidosis, which had preceded the diagnosis of MM and benefited from MM treatment. Faced with the suspicion of amyloidosis, if confirmed, this can be used to anticipate the diagnosis of MM, and at a more advanced stage, it can benefit from the treatment of the MM. |
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AbstractList | Amyloidosis is a rare disease that is often seen in conjunction with multiple myeloma (MM). Its damage varies depending on the anatomical site affected; however, it is believed that many cases of amyloidosis are misrecognized due to the fact that its signs and symptoms are nonspecific. Joint amyloidosis, in particular, may be confused with degenerative or autoimmune diseases. When it is associated with MM, it can significantly precede the diagnosis of the latter. We describe a case report of a woman of Nigerian heritage diagnosed with MM with widespread joint manifestations compatible with a diagnosis of amyloidosis, which had preceded the diagnosis of MM and benefited from MM treatment. Faced with the suspicion of amyloidosis, if confirmed, this can be used to anticipate the diagnosis of MM, and at a more advanced stage, it can benefit from the treatment of the MM. |
Author | De Tata, Vincenzo Galimberti, Sara Mazziotta, Francesco Benedetti, Edoardo Orciuolo, Enrico Masini, Matilde Del Giudice, Maria Livia Petrini, Mario Buda, Gabriele |
AuthorAffiliation | 2 Department of Translational Research and New Technologies in Medicine and Surgery, Pisa University Hospital, 56126 Pisa, Italy; matilde.masini@unipi.it (M.M.); vincenzo.detata@unipi.it (V.D.T.) 1 Hematology Division, Pisa University Hospital, 56126 Pisa, Italy; francemazziotta@gmail.com (F.M.); ga.buda@libero.it (G.B.); e.orciuolo@alumni.sssup.it (E.O.); edobenedetti@gmail.com (E.B.); sara.galimberti@unipi.it (S.G.); mario.petrini@unipi.it (M.P.) |
AuthorAffiliation_xml | – name: 1 Hematology Division, Pisa University Hospital, 56126 Pisa, Italy; francemazziotta@gmail.com (F.M.); ga.buda@libero.it (G.B.); e.orciuolo@alumni.sssup.it (E.O.); edobenedetti@gmail.com (E.B.); sara.galimberti@unipi.it (S.G.); mario.petrini@unipi.it (M.P.) – name: 2 Department of Translational Research and New Technologies in Medicine and Surgery, Pisa University Hospital, 56126 Pisa, Italy; matilde.masini@unipi.it (M.M.); vincenzo.detata@unipi.it (V.D.T.) |
Author_xml | – sequence: 1 givenname: Francesco surname: Mazziotta fullname: Mazziotta, Francesco organization: Hematology Division, Pisa University Hospital, 56126 Pisa, Italy – sequence: 2 givenname: Gabriele surname: Buda fullname: Buda, Gabriele organization: Hematology Division, Pisa University Hospital, 56126 Pisa, Italy – sequence: 3 givenname: Maria Livia orcidid: 0000-0003-4291-8875 surname: Del Giudice fullname: Del Giudice, Maria Livia organization: Hematology Division, Pisa University Hospital, 56126 Pisa, Italy – sequence: 4 givenname: Enrico surname: Orciuolo fullname: Orciuolo, Enrico organization: Hematology Division, Pisa University Hospital, 56126 Pisa, Italy – sequence: 5 givenname: Edoardo orcidid: 0000-0001-5295-2087 surname: Benedetti fullname: Benedetti, Edoardo organization: Hematology Division, Pisa University Hospital, 56126 Pisa, Italy – sequence: 6 givenname: Matilde surname: Masini fullname: Masini, Matilde organization: Department of Translational Research and New Technologies in Medicine and Surgery, Pisa University Hospital, 56126 Pisa, Italy – sequence: 7 givenname: Vincenzo surname: De Tata fullname: De Tata, Vincenzo organization: Department of Translational Research and New Technologies in Medicine and Surgery, Pisa University Hospital, 56126 Pisa, Italy – sequence: 8 givenname: Sara surname: Galimberti fullname: Galimberti, Sara organization: Hematology Division, Pisa University Hospital, 56126 Pisa, Italy – sequence: 9 givenname: Mario orcidid: 0000-0002-1017-6961 surname: Petrini fullname: Petrini, Mario organization: Hematology Division, Pisa University Hospital, 56126 Pisa, Italy |
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Cites_doi | 10.3109/13506129.2013.862229 10.1016/j.semarthrit.2013.07.004 10.1161/01.CIR.0000068314.02595.B2 10.3109/13506129.2015.1054026 10.1182/blood-2016-01-629790 10.1182/blood-2014-11-609883 10.1182/blood-2013-01-453001 10.1182/blood-2016-01-693580 |
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Copyright | 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2022 by the authors. 2022 |
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Keywords | multiple myeloma immunoglobulin light-chain amyloidosis joint diseases plasma cell neoplasm |
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References | Gras (ref_6) 2011; 752 Moreau (ref_7) 2016; 127 Elsaman (ref_8) 2013; 43 Palladini (ref_1) 2016; 128 Palladini (ref_4) 2003; 107 Pessler (ref_9) 2013; 21 Howie (ref_5) 2015; 22 Verga (ref_3) 2015; 125 Merlini (ref_2) 2013; 121 |
References_xml | – volume: 21 start-page: 28 year: 2013 ident: ref_9 article-title: Amyloid arthropathy associated with multiple myeloma: Polyarthritis without synovial infiltration of CD20+ or CD38+ cells publication-title: Amyloid doi: 10.3109/13506129.2013.862229 contributor: fullname: Pessler – volume: 752 start-page: 197 year: 2011 ident: ref_6 article-title: Transmission Electron Microscopy of Amyloid Fibrils publication-title: Program. Necrosis contributor: fullname: Gras – volume: 43 start-page: 405 year: 2013 ident: ref_8 article-title: Amyloid arthropathy associated with multiple myeloma: A systematic analysis of 101 reported cases publication-title: Semin. Arthritis Rheum. doi: 10.1016/j.semarthrit.2013.07.004 contributor: fullname: Elsaman – volume: 107 start-page: 2440 year: 2003 ident: ref_4 article-title: Serum N-Terminal Pro-Brain Natriuretic Peptide Is a Sensitive Marker of Myocardial Dysfunction in AL Amyloidosis publication-title: Circulation doi: 10.1161/01.CIR.0000068314.02595.B2 contributor: fullname: Palladini – volume: 22 start-page: 205 year: 2015 ident: ref_5 article-title: “Green (or apple-green) birefringence” of Congo red-stained amyloid publication-title: Amyloid doi: 10.3109/13506129.2015.1054026 contributor: fullname: Howie – volume: 128 start-page: 159 year: 2016 ident: ref_1 article-title: What is new in diagnosis and management of light chain amyloidosis? publication-title: Blood doi: 10.1182/blood-2016-01-629790 contributor: fullname: Palladini – volume: 125 start-page: 2239 year: 2015 ident: ref_3 article-title: A practical approach to the diagnosis of systemic amyloidoses publication-title: Blood doi: 10.1182/blood-2014-11-609883 contributor: fullname: Verga – volume: 121 start-page: 5124 year: 2013 ident: ref_2 article-title: Systemic light chain amyloidosis: An update for treating physicians publication-title: Blood doi: 10.1182/blood-2013-01-453001 contributor: fullname: Merlini – volume: 127 start-page: 2569 year: 2016 ident: ref_7 article-title: VTD is superior to VCD prior to intensive therapy in multiple myeloma: Results of the prospective IFM2013-04 trial publication-title: Blood doi: 10.1182/blood-2016-01-693580 contributor: fullname: Moreau |
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SubjectTerms | Amyloidosis Arthritis Autoimmune diseases Biopsy Bone marrow Case Report Conflicts of interest Diagnosis Hematology immunoglobulin light-chain amyloidosis joint diseases Light Literature reviews Medical imaging Microscopy Multiple myeloma Patients plasma cell neoplasm Stem cells Transplants & implants Ultrasonic imaging |
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Title | Joint Pain and Arthritis as First Clinical Manifestation of Systemic Amyloidosis and Multiple Myeloma: Case Report and Brief Literature Review |
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