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DOI: 10.1055/a-2732-6576
ATTR-Amyloidose für den Handchirurgen – eine versteckte, behandelbare Systemerkrankung
ATTR Amyloidosis for Hand Surgeons: A Hidden, Treatable Systemic DiseaseAuthors
Zusammenfassung
Es gibt deutliche Hinweise darauf, dass das Karpaltunnelsyndrom (CTS), insbesondere, wenn es bilateral, rezidivierend oder bei älteren Erwachsenen auftritt, häufig mit einer lebensgefährlichen Systemerkrankung, der Transthyretin (ATTR)-Amyloidose assoziiert ist. Es sollte daher als potenzielle Frühmanifestation der ATTR-Amyloidose erkannt werden und weitere Untersuchungen auf eine systemische ATTR-Amyloidose anstoßen. In diesem Artikel beleuchten wir die Bedeutung des CTS für die Amyloidose und weisen auf wichtige nächste Schritte in der Diagnostik hin, die bei Nachweis von Amyloid im Ligamentum carpi transversum unbedingt durchgeführt werden sollten. Diese beinhalten die histopathologische Subspezfizierung, die Untersuchung auf Leichtketten im Serum zum Ausschluss oder der raschen Behandlung einer AL-Amyloidose und insbesondere bei Symptomen einer Kardiomyopathie die Diagnostik einer kardialen Amyloidose sowie die genetische Testung bei Nachweis von ATTR-Amyloid. Zusammenfassend ist das Karpaltunnelsyndrom ein wichtiger erster Hinweis auf eine tödliche, aber behandelbare Systemerkrankung, die nicht übersehen werden sollte. Als Handchirurg sollte daher ein Augenmerk auf Patient:innen mit CTS gelegt werden und eine histopathologische Untersuchung des entnommenen Gewebes möglichst in die Routine integriert werden.
Abstract
There is strong evidence that carpal tunnel syndrome (CTS) – particularly when bilateral, recurrent or occurring in older adults – is frequently associated with a life-threatening systemic disease, transthyretin (ATTR) amyloidosis. It should, therefore, be recognised as a potential early manifestation of ATTR amyloidosis and prompt further investigations. In this article, we highlight the significance of CTS in the context of amyloidosis and emphasise the key diagnostic steps that should be taken when amyloid is detected in the transverse carpal ligament. These include histopathological subtyping, serum testing for light chains to rule out or enable rapid treatment of AL amyloidosis, and – especially in the presence of cardiomyopathic symptoms – diagnostic evaluation for cardiac amyloidosis as well as genetic testing in cases where ATTR amyloid is identified. In summary, carpal tunnel syndrome is an important early indication of a fatal yet treatable systemic disease that should not be overlooked. Hand surgeons should, therefore, pay particular attention to patients with CTS and, whenever possible, incorporate a histopathological examination of the excised tissue into routine practice.
Publication History
Received: 15 July 2025
Accepted: 18 October 2025
Article published online:
18 December 2025
© 2025. Thieme. All rights reserved.
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
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Literatur
- 1 Dohrn MF, Ihne S, Hegenbart U. et al. Targeting transthyretin – Mechanism-based treatment approaches and future perspectives in hereditary amyloidosis. J Neurochem 2021; 156: 802-818
- 2 Bergstrom J, Gustavsson A, Hellman U. et al. Amyloid deposits in transthyretin-derived amyloidosis: cleaved transthyretin is associated with distinct amyloid morphology. J Pathol 2005; 206: 224-232
- 3 Milandri A, Farioli A, Gagliardi C. et al. Carpal tunnel syndrome in cardiac amyloidosis: implications for early diagnosis and prognostic role across the spectrum of aetiologies. Eur J Heart Fail 2020; 22: 507-515
- 4 Palladini G, Milani P. Diagnosis and Treatment of AL Amyloidosis. Drugs 2023; 83: 203-216
- 5 Lin HM, Gao X, Cooke CE. et al. Disease burden of systemic light-chain amyloidosis: a systematic literature review. Curr Med Res Opin 2017; 33: 1017-1031
- 6 Thimm A, Carpinteiro A, Oubari S. et al. Prevalence and predictors of neurological manifestations in systemic AL amyloidosis. J Neurol Sci 2022; 440: 120341
- 7 Rowczenio DM, Noor I, Gillmore JD. et al. Online registry for mutations in hereditary amyloidosis including nomenclature recommendations. Hum Mutat 2014; 35: E2403-E2412
- 8 Vergaro G, Aimo A, Barison A. et al. Keys to early diagnosis of cardiac amyloidosis: red flags from clinical, laboratory and imaging findings. Eur J Prev Cardiol 2020; 27: 1806-1815
- 9 Andrade C. A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves. Brain 1952; 75: 408-427
- 10 Carvalho E, Dias A, Coelho T. et al. Hereditary transthyretin amyloidosis: a myriad of factors that influence phenotypic variability. J Neurol 2024; 271: 5746-5761
- 11 Ihse E, Ybo A, Suhr O. et al. Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis. J Pathol 2008; 216: 253-261
- 12 Aimo A, Vergaro G, Castiglione V. et al. Wild-type transthyretin cardiac amyloidosis is not rare in elderly subjects: the CATCH screening study. Eur J Prev Cardiol 2024; 31: 1410-1417
- 13 Ueda M, Horibata Y, Shono M. et al. Clinicopathological features of senile systemic amyloidosis: an ante- and post-mortem study. Mod Pathol 2011; 24: 1533-1544
- 14 Siepen FAD, Hein S, Prestel S. et al. Carpal tunnel syndrome and spinal canal stenosis: harbingers of transthyretin amyloid cardiomyopathy?. Clin Res Cardiol 2019; 108: 1324-1330
- 15 Kleefeld F, Scherret E, Knebel F. et al. Same same, but different? The neurological presentation of wildtype transthyretin (ATTRwt) amyloidosis. Amyloid 2022; 29: 92-101
- 16 Pernice HF, Knorz AL, Wetzel PJ. et al. Neurological affection and serum neurofilament light chain in wild type transthyretin amyloidosis. Sci Rep 2024; 14: 10111
- 17 Coutinho P, Martins da Silva A, Lopes Lima J, Resende Barbosa A. Forty years of experience with type I amyloidneuropathy. Review of 483 cases. Amsterdam: Excerpta Medica. 1980
- 18 Fontana M, Berk JL, Gillmore JD. et al. Vutrisiran in Patients with Transthyretin Amyloidosis with Cardiomyopathy. N Engl J Med. 2024
- 19 Maurer MS, Schwartz JH, Gundapaneni B. et al. Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy. New Engl J Med 2018; 379: 1007-1016
- 20 Gillmore JD, Judge DP, Cappelli F. et al. Efficacy and Safety of Acoramidis in Transthyretin Amyloid Cardiomyopathy. N Engl J Med 2024; 390: 132-142
- 21 Coelho T, Maia LF, da Silva AM. et al. Tafamidis for transthyretin familial amyloid polyneuropathy A randomized, controlled trial. Neurology 2012; 79: 785-792
- 22 Adams D, Gonzalez-Duarte A, O'Riordan WD. et al. Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis. N Engl J Med 2018; 379: 11-21
- 23 Adams D, Tournev IL, Taylor MS. et al. Efficacy and safety of vutrisiran for patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy: a randomized clinical trial. Amyloid 2023; 30: 1-9
- 24 Coelho T, Marques W, Dasgupta NR. et al. Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy. JAMA 2023; 330: 1448-1458
- 25 Benson MD, Waddington-Cruz M, Berk JL. et al. Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis. N Engl J Med 2018; 379: 22-31
- 26 Ioannou A, Patel RK, Razvi Y. et al. Impact of Earlier Diagnosis in Cardiac ATTR Amyloidosis Over the Course of 20 Years. Circulation 2022; 146: 1657-1670
- 27 Russell A, Khayambashi S, Fine NM. et al. Characteristics of Carpal Tunnel Syndrome in Wild-Type Transthyretin Amyloidosis. Can J Neurol Sci 2024; 51: 482-486
- 28 Sperry BW, Jones BM, Vranian MN. et al. Recognizing Transthyretin Cardiac Amyloidosis in Patients With Aortic Stenosis: Impact on Prognosis. JACC Cardiovasc Imaging 2016; 9: 904-906
- 29 Westin O, Fosbøl EL, Maurer MS. et al. Screening for Cardiac Amyloidosis 5 to 15 Years After Surgery for Bilateral Carpal Tunnel Syndrome. J Am Coll Cardiol 2022; 80: 967-977
- 30 Donnelly JP, Hanna M, Sperry BW. et al. Carpal Tunnel Syndrome: A Potential Early, Red-Flag Sign of Amyloidosis. J Hand Surg Am 2019; 44: 868-876
- 31 Lin TY, Chang KV, Wu WT. et al. Ultrasonography for the diagnosis of carpal tunnel syndrome: an umbrella review. J Neurol 2022; 269: 4663-4675
- 32 Salvalaggio A, Coraci D, Cacciavillani M. et al. Nerve ultrasound in hereditary transthyretin amyloidosis: red flags and possible progression biomarkers. J Neurol 2021; 268: 189-198
- 33 Podnar S, Sarafov S, Tournev I. et al. Peripheral nerve ultrasonography in patients with transthyretin amyloidosis. Clin Neurophysiol 2017; 128: 505-511
- 34 Sperry BW, Reyes BA, Ikram A. et al. Tenosynovial and Cardiac Amyloidosis in Patients Undergoing Carpal Tunnel Release. J Am Coll Cardiol 2018; 72: 2040-2050
- 35 Hahn K, Urban P, Meliss RR. et al. [Carpal tunnel syndrome and ATTR-amyloidosis]. Handchir Mikrochir Plast Chir 2018; 50: 329-334
- 36 Doneddu PE, Moretti G, Di Stefano V. et al. Prevalence of hereditary transthyretin amyloidosis in CIDP patients with red flags: a multicenter genetic screening and misdiagnosis analysis. J Neurol 2025; 272: 515
- 37 Karam C, Dimitrova D, Christ M. et al. Carpal tunnel syndrome and associated symptoms as first manifestation of hATTR amyloidosis. Neurol Clin Pract 2019; 9: 309-313
