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Published in: BMC Musculoskeletal Disorders 1/2021

Open Access 01-12-2021 | Carpal Tunnel Syndrome | Research article

Musculoskeletal pathology as an early warning sign of systemic amyloidosis: a systematic review of amyloid deposition and orthopedic surgery

Authors: Austin E. Wininger, Brian M. Phelps, Jessica T. Le, Joshua D. Harris, Barry H. Trachtenberg, Shari R. Liberman

Published in: BMC Musculoskeletal Disorders | Issue 1/2021

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Abstract

Background

Transthyretin and immunoglobulin light-chain amyloidoses cause amyloid deposition throughout various organ systems. Recent evidence suggests that soft tissue amyloid deposits may lead to orthopedic conditions before cardiac manifestations occur. Pharmacologic treatments reduce further amyloid deposits in these patients. Thus, early diagnosis improves long term survival.

Questions/purposes

The primary purpose of this systematic review was to characterize the association between amyloid deposition and musculoskeletal pathology in patients with common orthopedic conditions. A secondary purpose was to determine the relationship between amyloid positive biopsy in musculoskeletal tissue and the eventual diagnosis of systemic amyloidosis.

Methods

We performed a systematic review using PRISMA guidelines. Inclusion criteria were level I-IV evidence articles that analyzed light-chain or transthyretin amyloid deposits in common orthopedic surgeries. Study methodological quality, risk of bias, and recommendation strength were assessed using MINORS, ROBINS-I, and SORT.

Results

This systematic review included 24 studies for final analysis (3606 subjects). Amyloid deposition was reported in five musculoskeletal pathologies, including carpal tunnel syndrome (transverse carpal ligament and flexor tenosynovium), hip and knee osteoarthritis (synovium and articular cartilage), lumbar spinal stenosis (ligamentum flavum), and rotator cuff tears (tendon). A majority of studies reported a mean age greater than 70 for patients with TTR or AL positive amyloid.

Conclusions

This systematic review has shown the presence of amyloid deposition detected at the time of common orthopedic surgeries, especially in patients ≥70 years old. Subtyping of the amyloid has been shown to enable diagnosis of systemic light-chain or transthyretin amyloidosis prior to cardiac manifestations.

Level of evidence

Level IV.
Appendix
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Literature
1.
go back to reference Siddiqi OK, Ruberg FL. Cardiac amyloidosis: an update on pathophysiology, diagnosis, and treatment. Trends Cardiovasc Med. 2018;28(1):10–21.PubMedCrossRef Siddiqi OK, Ruberg FL. Cardiac amyloidosis: an update on pathophysiology, diagnosis, and treatment. Trends Cardiovasc Med. 2018;28(1):10–21.PubMedCrossRef
2.
go back to reference Sipe JD, Benson MD, Buxbaum JN, et al. Nomenclature 2014: amyloid fibril proteins and clinical classification of the amyloidosis. Amyloid. 2014;21(4):221–4.PubMedCrossRef Sipe JD, Benson MD, Buxbaum JN, et al. Nomenclature 2014: amyloid fibril proteins and clinical classification of the amyloidosis. Amyloid. 2014;21(4):221–4.PubMedCrossRef
3.
4.
go back to reference Maurer MS, Elliott P, Comenzo R, et al. Addressing common questions encountered in the diagnosis and Management of Cardiac Amyloidosis. Circulation. 2017;135(14):1357–77.PubMedPubMedCentralCrossRef Maurer MS, Elliott P, Comenzo R, et al. Addressing common questions encountered in the diagnosis and Management of Cardiac Amyloidosis. Circulation. 2017;135(14):1357–77.PubMedPubMedCentralCrossRef
5.
6.
go back to reference Maurer MS, Hanna M, Grogan M, et al. Genotype and phenotype of Transthyretin cardiac amyloidosis: THAOS (Transthyretin amyloid outcome survey). J Am Coll Cardiol. 2016;68(2):161–72.PubMedPubMedCentralCrossRef Maurer MS, Hanna M, Grogan M, et al. Genotype and phenotype of Transthyretin cardiac amyloidosis: THAOS (Transthyretin amyloid outcome survey). J Am Coll Cardiol. 2016;68(2):161–72.PubMedPubMedCentralCrossRef
7.
go back to reference Rapezzi C, Merlini G, Quarta CC, et al. Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types. Circulation. 2009;120(13):1203–12.PubMedCrossRef Rapezzi C, Merlini G, Quarta CC, et al. Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types. Circulation. 2009;120(13):1203–12.PubMedCrossRef
8.
go back to reference Lane T, Fontana M, Martinez-Naharro A, et al. Natural history, quality of life, and outcome in cardiac Transthyretin amyloidosis. Circulation. 2019;140(1):16–26.PubMedCrossRef Lane T, Fontana M, Martinez-Naharro A, et al. Natural history, quality of life, and outcome in cardiac Transthyretin amyloidosis. Circulation. 2019;140(1):16–26.PubMedCrossRef
9.
go back to reference Grogan M, Dispenzieri A, Gertz MA. Light-chain cardiac amyloidosis: strategies to promote early diagnosis and cardiac response. Heart. 2017;103(14):1065–72.PubMedCrossRef Grogan M, Dispenzieri A, Gertz MA. Light-chain cardiac amyloidosis: strategies to promote early diagnosis and cardiac response. Heart. 2017;103(14):1065–72.PubMedCrossRef
10.
go back to reference Sperry BW, Tang WHW. Amyloid heart disease: genetics translated into disease-modifying therapy. Heart. 2017;103(11):812–7.PubMedCrossRef Sperry BW, Tang WHW. Amyloid heart disease: genetics translated into disease-modifying therapy. Heart. 2017;103(11):812–7.PubMedCrossRef
11.
go back to reference Vranian MN, Sperry BW, Valent J, Hanna M. Emerging advances in the Management of Cardiac Amyloidosis. Curr Cardiol Rep. 2015;17(11):100.PubMedCrossRef Vranian MN, Sperry BW, Valent J, Hanna M. Emerging advances in the Management of Cardiac Amyloidosis. Curr Cardiol Rep. 2015;17(11):100.PubMedCrossRef
12.
go back to reference Prokaeva T, Spencer B, Kaut M, et al. Soft tissue, joint, and bone manifestations of AL amyloidosis: clinical presentation, molecular features, and survival. Arthritis Rheum. 2007;56(11):3858–68.PubMedCrossRef Prokaeva T, Spencer B, Kaut M, et al. Soft tissue, joint, and bone manifestations of AL amyloidosis: clinical presentation, molecular features, and survival. Arthritis Rheum. 2007;56(11):3858–68.PubMedCrossRef
13.
go back to reference Sueyoshi T, Ueda M, Jono H, et al. Wild-type transthyretin-derived amyloidosis in various ligaments and tendons. Hum Pathol. 2011;42(9):1259–64.PubMedCrossRef Sueyoshi T, Ueda M, Jono H, et al. Wild-type transthyretin-derived amyloidosis in various ligaments and tendons. Hum Pathol. 2011;42(9):1259–64.PubMedCrossRef
14.
go back to reference Gioeva Z, Urban P, Meliss RR, et al. ATTR amyloid in the carpal tunnel ligament is frequently of wildtype transthyretin origin. Amyloid. 2013;20(1):1–6.PubMedCrossRef Gioeva Z, Urban P, Meliss RR, et al. ATTR amyloid in the carpal tunnel ligament is frequently of wildtype transthyretin origin. Amyloid. 2013;20(1):1–6.PubMedCrossRef
15.
go back to reference Bishop E, Brown EE, Fajardo J, et al. Seven factors predict a delayed diagnosis of cardiac amyloidosis. Amyloid. 2018;25(3):174–9.PubMedCrossRef Bishop E, Brown EE, Fajardo J, et al. Seven factors predict a delayed diagnosis of cardiac amyloidosis. Amyloid. 2018;25(3):174–9.PubMedCrossRef
16.
go back to reference Kyle RA, Eilers SG, Linscheid RL, Gaffey TA. Amyloid localized to tenosynovium at carpal tunnel release. Natural history of 124 cases. Am J Clin Pathol. 1989;91(4):393–7.PubMedCrossRef Kyle RA, Eilers SG, Linscheid RL, Gaffey TA. Amyloid localized to tenosynovium at carpal tunnel release. Natural history of 124 cases. Am J Clin Pathol. 1989;91(4):393–7.PubMedCrossRef
17.
go back to reference Nakagawa M, Sekijima Y, Yazaki M, et al. Carpal tunnel syndrome: a common initial symptom of systemic wild-type ATTR (ATTRwt) amyloidosis. Amyloid. 2016;23(1):58–63.PubMedCrossRef Nakagawa M, Sekijima Y, Yazaki M, et al. Carpal tunnel syndrome: a common initial symptom of systemic wild-type ATTR (ATTRwt) amyloidosis. Amyloid. 2016;23(1):58–63.PubMedCrossRef
18.
go back to reference Sekijima Y, Uchiyama S, Tojo K, et al. High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderly. Hum Pathol. 2011;42(11):1785–91.PubMedCrossRef Sekijima Y, Uchiyama S, Tojo K, et al. High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderly. Hum Pathol. 2011;42(11):1785–91.PubMedCrossRef
19.
go back to reference Donnelly JP, Hanna M, Sperry BW, Seitz WH. Carpal tunnel syndrome: a potential early, red-flag sign of amyloidosis. J Hand Surg Am. 2019;44(10):868–76.PubMedCrossRef Donnelly JP, Hanna M, Sperry BW, Seitz WH. Carpal tunnel syndrome: a potential early, red-flag sign of amyloidosis. J Hand Surg Am. 2019;44(10):868–76.PubMedCrossRef
20.
go back to reference Westermark P, Westermark GT, Suhr OB, Berg S. Transthyretin-derived amyloidosis: probably a common cause of lumbar spinal stenosis. Ups J Med Sci. 2014;119(3):223–8.PubMedPubMedCentralCrossRef Westermark P, Westermark GT, Suhr OB, Berg S. Transthyretin-derived amyloidosis: probably a common cause of lumbar spinal stenosis. Ups J Med Sci. 2014;119(3):223–8.PubMedPubMedCentralCrossRef
21.
go back to reference Yanagisawa A, Ueda M, Sueyoshi T, et al. Amyloid deposits derived from transthyretin in the ligamentum flavum as related to lumbar spinal canal stenosis. Mod Pathol. 2015;28(2):201–7.PubMedCrossRef Yanagisawa A, Ueda M, Sueyoshi T, et al. Amyloid deposits derived from transthyretin in the ligamentum flavum as related to lumbar spinal canal stenosis. Mod Pathol. 2015;28(2):201–7.PubMedCrossRef
22.
go back to reference Goffin YA. The association of amyloid deposits and osteoarthritis. Arthritis Rheum. 1983;26(1):120.PubMedCrossRef Goffin YA. The association of amyloid deposits and osteoarthritis. Arthritis Rheum. 1983;26(1):120.PubMedCrossRef
23.
go back to reference Gu YJ, Ge P, Mu Y, Lu JH, Zheng F, Sun XG. Clinical and laboratory characteristics of patients having amyloidogenic transthyretin deposition in osteoarthritic knee joints. J Zhejiang Univ Sci B. 2014;15(1):92–9.PubMedPubMedCentralCrossRef Gu YJ, Ge P, Mu Y, Lu JH, Zheng F, Sun XG. Clinical and laboratory characteristics of patients having amyloidogenic transthyretin deposition in osteoarthritic knee joints. J Zhejiang Univ Sci B. 2014;15(1):92–9.PubMedPubMedCentralCrossRef
25.
go back to reference Takanashi T, Matsuda M, Yazaki M, et al. Synovial deposition of wild-type transthyretin-derived amyloid in knee joint osteoarthritis patients. Amyloid. 2013;20(3):151–5.PubMedCrossRef Takanashi T, Matsuda M, Yazaki M, et al. Synovial deposition of wild-type transthyretin-derived amyloid in knee joint osteoarthritis patients. Amyloid. 2013;20(3):151–5.PubMedCrossRef
26.
go back to reference Yanagisawa A, Ueda M, Sueyoshi T, et al. Knee osteoarthritis associated with different kinds of amyloid deposits and the impact of aging on type of amyloid. Amyloid. 2016;23(1):26–32.PubMedCrossRef Yanagisawa A, Ueda M, Sueyoshi T, et al. Knee osteoarthritis associated with different kinds of amyloid deposits and the impact of aging on type of amyloid. Amyloid. 2016;23(1):26–32.PubMedCrossRef
27.
go back to reference Rubin J, Alvarez J, Teruya S, et al. Hip and knee arthroplasty are common among patients with transthyretin cardiac amyloidosis, occurring years before cardiac amyloid diagnosis: can we identify affected patients earlier? Amyloid. 2017;24(4):226–30.PubMedCrossRef Rubin J, Alvarez J, Teruya S, et al. Hip and knee arthroplasty are common among patients with transthyretin cardiac amyloidosis, occurring years before cardiac amyloid diagnosis: can we identify affected patients earlier? Amyloid. 2017;24(4):226–30.PubMedCrossRef
28.
go back to reference Nguyen TX, Naqvi A, Thompson TL, Wilson RH. Musculoskeletal manifestations of amyloidosis: a focused review. J Surg Orthop Adv. 2018;27(1):1–5.PubMed Nguyen TX, Naqvi A, Thompson TL, Wilson RH. Musculoskeletal manifestations of amyloidosis: a focused review. J Surg Orthop Adv. 2018;27(1):1–5.PubMed
29.
go back to reference Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Br Med J. 2009;339:b2535.CrossRef Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Br Med J. 2009;339:b2535.CrossRef
30.
go back to reference Harris JD, Quatman CE, Manring MM, et al. How to write a systematic review. Am J Sports Med. 2014;42(11):2761–8.PubMedCrossRef Harris JD, Quatman CE, Manring MM, et al. How to write a systematic review. Am J Sports Med. 2014;42(11):2761–8.PubMedCrossRef
31.
go back to reference Marx RG, Wilson SM, Swiontkowski MF. Updating the assignment of levels of evidence. J Bone Joint Surg Am. 2015;97(1):1–2.PubMedCrossRef Marx RG, Wilson SM, Swiontkowski MF. Updating the assignment of levels of evidence. J Bone Joint Surg Am. 2015;97(1):1–2.PubMedCrossRef
32.
go back to reference Slim K, Nini E, Forestier D, et al. Methodological index for non-randomized studies (minors): development and validation of a new instrument. ANZ J Surg. 2003;73(9):712–6.PubMedCrossRef Slim K, Nini E, Forestier D, et al. Methodological index for non-randomized studies (minors): development and validation of a new instrument. ANZ J Surg. 2003;73(9):712–6.PubMedCrossRef
33.
34.
go back to reference Ebell MH, Siwek J, Weiss BD, et al. Strength of recommendation taxonomy (SORT): a patient-centered approach to grading evidence in the medical literature. J Am Board Fam Pract. 2004;17(1):59–67.PubMedCrossRef Ebell MH, Siwek J, Weiss BD, et al. Strength of recommendation taxonomy (SORT): a patient-centered approach to grading evidence in the medical literature. J Am Board Fam Pract. 2004;17(1):59–67.PubMedCrossRef
35.
go back to reference Akasaki Y, Reixach N, Matsuzaki T, et al. Transthyretin deposition in articular cartilage: a novel mechanism in the pathogenesis of osteoarthritis. Arthritis Rheumatol. 2015;67(8):2097–107.PubMedPubMedCentralCrossRef Akasaki Y, Reixach N, Matsuzaki T, et al. Transthyretin deposition in articular cartilage: a novel mechanism in the pathogenesis of osteoarthritis. Arthritis Rheumatol. 2015;67(8):2097–107.PubMedPubMedCentralCrossRef
36.
go back to reference Aus dem siepen F, Hein S, Prestel S, et al. Carpal tunnel syndrome and spinal canal stenosis: harbingers of transthyretin amyloid cardiomyopathy? Clin Res Cardiol. 2019;108(12):1324–30.CrossRef Aus dem siepen F, Hein S, Prestel S, et al. Carpal tunnel syndrome and spinal canal stenosis: harbingers of transthyretin amyloid cardiomyopathy? Clin Res Cardiol. 2019;108(12):1324–30.CrossRef
37.
go back to reference Fuertes JF, Vicente ÓR, Herráez SS, Pascua LR. Early diagnosis of systemic amyloidosis by means of a transverse carpal ligament biopsy carried out during carpal tunnel syndrome surgery. Med Clin (Barc). 2017;148(5):211–4. Fuertes JF, Vicente ÓR, Herráez SS, Pascua LR. Early diagnosis of systemic amyloidosis by means of a transverse carpal ligament biopsy carried out during carpal tunnel syndrome surgery. Med Clin (Barc). 2017;148(5):211–4.
38.
go back to reference Geller HI, Singh A, Alexander KM, et al. Association between ruptured distal biceps tendon and wild-type Transthyretin cardiac amyloidosis. JAMA. 2017;318(10):962–3.PubMedPubMedCentralCrossRef Geller HI, Singh A, Alexander KM, et al. Association between ruptured distal biceps tendon and wild-type Transthyretin cardiac amyloidosis. JAMA. 2017;318(10):962–3.PubMedPubMedCentralCrossRef
39.
go back to reference Gies U, Linke RP, Schachenmayr W. Amyloid deposits of immunohistochemically different classes in the ligamentum flavum in biopsies from patients with herniated discs or lumbar spinal stenosis. Clin Neuropathol. 1996;15(1):54–9.PubMed Gies U, Linke RP, Schachenmayr W. Amyloid deposits of immunohistochemically different classes in the ligamentum flavum in biopsies from patients with herniated discs or lumbar spinal stenosis. Clin Neuropathol. 1996;15(1):54–9.PubMed
40.
go back to reference Kyle RA, Gertz MA, Linke RP. Amyloid localized to tenosynovium at carpal tunnel release. Immunohistochemical identification of amyloid type. Am J Clin Pathol. 1992;97(2):250–3.PubMedCrossRef Kyle RA, Gertz MA, Linke RP. Amyloid localized to tenosynovium at carpal tunnel release. Immunohistochemical identification of amyloid type. Am J Clin Pathol. 1992;97(2):250–3.PubMedCrossRef
41.
go back to reference Nakamichi KI, Tachibana S. Amyloid deposition in the synovium and ligament in idiopathic carpal tunnel syndrome. Muscle Nerve. 1996;19(10):1349–51.PubMedCrossRef Nakamichi KI, Tachibana S. Amyloid deposition in the synovium and ligament in idiopathic carpal tunnel syndrome. Muscle Nerve. 1996;19(10):1349–51.PubMedCrossRef
42.
go back to reference Niggemeyer O, Steinhagen J, Deuretzbacher G, et al. Amyloid deposition in osteoarthritis of the hip. Arch Orthop Trauma Surg. 2011;131(5):637–43.PubMedCrossRef Niggemeyer O, Steinhagen J, Deuretzbacher G, et al. Amyloid deposition in osteoarthritis of the hip. Arch Orthop Trauma Surg. 2011;131(5):637–43.PubMedCrossRef
43.
go back to reference Samões R, Taipa R, Valdrez K, et al. Amyloid detection in the transverse carpal ligament of patients with hereditary ATTR V30M amyloidosis and carpal tunnel syndrome. Amyloid. 2017;24(2):73–7.PubMedCrossRef Samões R, Taipa R, Valdrez K, et al. Amyloid detection in the transverse carpal ligament of patients with hereditary ATTR V30M amyloidosis and carpal tunnel syndrome. Amyloid. 2017;24(2):73–7.PubMedCrossRef
44.
go back to reference Scott KL, Conley CR, Renfree KJ. Histopathologic evaluation of flexor Tenosynovium in recurrent carpal tunnel syndrome. Plast Reconstr Surg. 2019;143(1):169–75.PubMedCrossRef Scott KL, Conley CR, Renfree KJ. Histopathologic evaluation of flexor Tenosynovium in recurrent carpal tunnel syndrome. Plast Reconstr Surg. 2019;143(1):169–75.PubMedCrossRef
45.
go back to reference Sperry BW, Reyes BA, Ikram A, et al. Tenosynovial and cardiac amyloidosis in patients undergoing carpal tunnel release. J Am Coll Cardiol. 2018;72(17):2040–50.PubMedCrossRef Sperry BW, Reyes BA, Ikram A, et al. Tenosynovial and cardiac amyloidosis in patients undergoing carpal tunnel release. J Am Coll Cardiol. 2018;72(17):2040–50.PubMedCrossRef
46.
go back to reference Stein K, Störkel S, Linke RP, Goebel HH. Chemical heterogeneity of amyloid in the carpal tunnel syndrome. Virchows Arch A Pathol Anat Histopathol. 1987;412(1):37–45.PubMedCrossRef Stein K, Störkel S, Linke RP, Goebel HH. Chemical heterogeneity of amyloid in the carpal tunnel syndrome. Virchows Arch A Pathol Anat Histopathol. 1987;412(1):37–45.PubMedCrossRef
47.
go back to reference Uchihara Y, Iwata E, Papadimitriou-olivgeri I, et al. Localised foot and ankle amyloid deposition. Pathol Res Pract. 2018;214(10):1661–6.PubMedCrossRef Uchihara Y, Iwata E, Papadimitriou-olivgeri I, et al. Localised foot and ankle amyloid deposition. Pathol Res Pract. 2018;214(10):1661–6.PubMedCrossRef
48.
go back to reference Zegri-reiriz I, de Daro-Del Moral FJ, Dominguez F, et al. Prevalence of cardiac amyloidosis in patients with carpal tunnel syndrome. J Cardiovasc Transl Res. 2019;12(6):507–13.PubMedCrossRef Zegri-reiriz I, de Daro-Del Moral FJ, Dominguez F, et al. Prevalence of cardiac amyloidosis in patients with carpal tunnel syndrome. J Cardiovasc Transl Res. 2019;12(6):507–13.PubMedCrossRef
50.
go back to reference González-lópez E, Gallego-delgado M, Guzzo-merello G, et al. Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction. Eur Heart J. 2015;36(38):2585–94.PubMedCrossRef González-lópez E, Gallego-delgado M, Guzzo-merello G, et al. Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction. Eur Heart J. 2015;36(38):2585–94.PubMedCrossRef
51.
go back to reference Longhi S, Guidalotti PL, Quarta CC, et al. Identification of TTR-related subclinical amyloidosis with 99mTc-DPD scintigraphy. JACC Cardiovasc Imaging. 2014;7(5):531–2.PubMedCrossRef Longhi S, Guidalotti PL, Quarta CC, et al. Identification of TTR-related subclinical amyloidosis with 99mTc-DPD scintigraphy. JACC Cardiovasc Imaging. 2014;7(5):531–2.PubMedCrossRef
52.
go back to reference Castaño A, Drachman BM, Judge D, Maurer MS. Natural history and therapy of TTR-cardiac amyloidosis: emerging disease-modifying therapies from organ transplantation to stabilizer and silencer drugs. Heart Fail Rev. 2015;20(2):163–78.PubMedPubMedCentralCrossRef Castaño A, Drachman BM, Judge D, Maurer MS. Natural history and therapy of TTR-cardiac amyloidosis: emerging disease-modifying therapies from organ transplantation to stabilizer and silencer drugs. Heart Fail Rev. 2015;20(2):163–78.PubMedPubMedCentralCrossRef
53.
go back to reference Ando Y, Ueda M. Diagnosis and therapeutic approaches to transthyretin amyloidosis. Curr Med Chem. 2012;19(15):2312–23.PubMedCrossRef Ando Y, Ueda M. Diagnosis and therapeutic approaches to transthyretin amyloidosis. Curr Med Chem. 2012;19(15):2312–23.PubMedCrossRef
54.
go back to reference Gertz MA, Mauermann ML, Grogan M, Coelho T. Advances in the treatment of hereditary transthyretin amyloidosis: a review. Brain Behav. 2019;9(9):e01371.PubMedPubMedCentralCrossRef Gertz MA, Mauermann ML, Grogan M, Coelho T. Advances in the treatment of hereditary transthyretin amyloidosis: a review. Brain Behav. 2019;9(9):e01371.PubMedPubMedCentralCrossRef
Metadata
Title
Musculoskeletal pathology as an early warning sign of systemic amyloidosis: a systematic review of amyloid deposition and orthopedic surgery
Authors
Austin E. Wininger
Brian M. Phelps
Jessica T. Le
Joshua D. Harris
Barry H. Trachtenberg
Shari R. Liberman
Publication date
01-12-2021
Publisher
BioMed Central
Published in
BMC Musculoskeletal Disorders / Issue 1/2021
Electronic ISSN: 1471-2474
DOI
https://doi.org/10.1186/s12891-020-03912-z

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