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Cardiac amyloidosis = diagnosis and treatment /

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Cardiac amyloidosis/ edited by Michele Emdin ... [et al.].
其他題名:	diagnosis and treatment /
其他作者:	Emdin, Michele.
出版者:	Cham :Springer Nature Switzerland : : 2024.,
面頁冊數:	viii, 324 p. :ill. (some col.), digital ;24 cm.
內容註:	1. Tribute to Claudio Rapezzi -- 2. Giampaolo Merlini and the Pavia School -- 3. A brief history of amyloidosis -- 4. Pathophysiology, classification and epidemiology of amyloidosis -- 5. Amyloid light chain (AL) amyloidosis -- 6. Hereditary transthyretin amyloidosis -- 7. Wild-type ATTR amyloidosis -- 8. Electrocardiographic patterns -- 9. Echocardiography: a gatekeeper to diagnosis -- 10. Cardiovascular magnetic resonance: characterization of myocardial involvement -- 11. Biomarkers: monoclonal protein and indicators of cardiac damage -- 12. Plasma transthyretin and its ligands -- 13. Cardiac Scintigraphy with Bone-Avid Tracers - Old and New Applications -- 14. PET-CT: a tool for etiological diagnosis -- 15. The role of tissue biopsy: identification of the amyloid precursor and beyond -- 16. From red flags to diagnosis -- 17. Risk prediction and follow-up -- 18. Differential diagnoses in clinical mimics -- 19. Applications of Artificial Intelligence in Amyloidosis -- 20. Treatment of amyloid light-chain amyloidosis -- 21. Treatment of ATTR amyloidosis: from stabilizers to gene-editing -- 22. Treatment of cardiac complications -- 23. Monitoring disease progression and response to disease-modifying treatments -- 24. Cardiac amyloidosis: open issues and future perspectives.
Contained By:	Springer Nature eBook
標題:	Heart - Diseases -
電子資源:	https://doi.org/10.1007/978-3-031-51757-0
ISBN:	9783031517570

Cardiac amyloidosis = diagnosis and treatment /
Cardiac amyloidosisdiagnosis and treatment /[electronic resource] :edited by Michele Emdin ... [et al.]. - Cham :Springer Nature Switzerland :2024. - viii, 324 p. :ill. (some col.), digital ;24 cm.

1. Tribute to Claudio Rapezzi -- 2. Giampaolo Merlini and the Pavia School -- 3. A brief history of amyloidosis -- 4. Pathophysiology, classification and epidemiology of amyloidosis -- 5. Amyloid light chain (AL) amyloidosis -- 6. Hereditary transthyretin amyloidosis -- 7. Wild-type ATTR amyloidosis -- 8. Electrocardiographic patterns -- 9. Echocardiography: a gatekeeper to diagnosis -- 10. Cardiovascular magnetic resonance: characterization of myocardial involvement -- 11. Biomarkers: monoclonal protein and indicators of cardiac damage -- 12. Plasma transthyretin and its ligands -- 13. Cardiac Scintigraphy with Bone-Avid Tracers - Old and New Applications -- 14. PET-CT: a tool for etiological diagnosis -- 15. The role of tissue biopsy: identification of the amyloid precursor and beyond -- 16. From red flags to diagnosis -- 17. Risk prediction and follow-up -- 18. Differential diagnoses in clinical mimics -- 19. Applications of Artificial Intelligence in Amyloidosis -- 20. Treatment of amyloid light-chain amyloidosis -- 21. Treatment of ATTR amyloidosis: from stabilizers to gene-editing -- 22. Treatment of cardiac complications -- 23. Monitoring disease progression and response to disease-modifying treatments -- 24. Cardiac amyloidosis: open issues and future perspectives.

Cardiac amyloidosis (CA) is caused by the accumulation of amyloid fibrils in the extracellular space of the myocardium, with clinical manifestations including conduction disturbances and heart failure. CA has traditionally been considered a rare disease, lacking effective therapies and with a poor prognosis, but in recent years, increased possibilities for non-invasive diagnosis and greater awareness of the disease have led to the identification of a growing number of cases, challenging the concept of CA as a rare disease. This is why the ability to recognise and manage patients with CA should become part of the core curriculum of cardiologists, but also of internal medicine specialists, neurologists, nephrologists, haematologists, and general practitioners. This book, written by leading experts in the field, will provide the state-of-the-art in the diagnosis and management of CA and will also discuss the latest research developments and future research directions. The volume appears to be a timely one, given the great interest of clinicians and researchers in CA and the exponential increase in publications in recent year, and will be of interest to cardiologists, internal medicine and other disciplines specialists who may encounter patients with CA in their clinical practice, as well as general practitioners.

ISBN: 9783031517570

Standard No.: 10.1007/978-3-031-51757-0doiSubjects--Topical Terms:

861315
Heart
--Diseases

LC Class. No.: RC683

Dewey Class. No.: 616.12075

Cardiac amyloidosis = diagnosis and treatment /
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505 0 $a 1. Tribute to Claudio Rapezzi -- 2. Giampaolo Merlini and the Pavia School -- 3. A brief history of amyloidosis -- 4. Pathophysiology, classification and epidemiology of amyloidosis -- 5. Amyloid light chain (AL) amyloidosis -- 6. Hereditary transthyretin amyloidosis -- 7. Wild-type ATTR amyloidosis -- 8. Electrocardiographic patterns -- 9. Echocardiography: a gatekeeper to diagnosis -- 10. Cardiovascular magnetic resonance: characterization of myocardial involvement -- 11. Biomarkers: monoclonal protein and indicators of cardiac damage -- 12. Plasma transthyretin and its ligands -- 13. Cardiac Scintigraphy with Bone-Avid Tracers - Old and New Applications -- 14. PET-CT: a tool for etiological diagnosis -- 15. The role of tissue biopsy: identification of the amyloid precursor and beyond -- 16. From red flags to diagnosis -- 17. Risk prediction and follow-up -- 18. Differential diagnoses in clinical mimics -- 19. Applications of Artificial Intelligence in Amyloidosis -- 20. Treatment of amyloid light-chain amyloidosis -- 21. Treatment of ATTR amyloidosis: from stabilizers to gene-editing -- 22. Treatment of cardiac complications -- 23. Monitoring disease progression and response to disease-modifying treatments -- 24. Cardiac amyloidosis: open issues and future perspectives.
520 $a Cardiac amyloidosis (CA) is caused by the accumulation of amyloid fibrils in the extracellular space of the myocardium, with clinical manifestations including conduction disturbances and heart failure. CA has traditionally been considered a rare disease, lacking effective therapies and with a poor prognosis, but in recent years, increased possibilities for non-invasive diagnosis and greater awareness of the disease have led to the identification of a growing number of cases, challenging the concept of CA as a rare disease. This is why the ability to recognise and manage patients with CA should become part of the core curriculum of cardiologists, but also of internal medicine specialists, neurologists, nephrologists, haematologists, and general practitioners. This book, written by leading experts in the field, will provide the state-of-the-art in the diagnosis and management of CA and will also discuss the latest research developments and future research directions. The volume appears to be a timely one, given the great interest of clinicians and researchers in CA and the exponential increase in publications in recent year, and will be of interest to cardiologists, internal medicine and other disciplines specialists who may encounter patients with CA in their clinical practice, as well as general practitioners.
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