Cardiac amyloidosis history and symptoms: Difference between revisions

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==Symptoms==
==Symptoms==
Cardiac amyloid cab be associated with the following symptoms:<ref name="pmid9578896">{{cite journal |author=Dubrey SW, Cha K, Anderson J, ''et al.'' |title=The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement |journal=[[QJM : Monthly Journal of the Association of Physicians]] |volume=91 |issue=2 |pages=141–57 |year=1998 |month=February |pmid=9578896 |doi= |url=}}</ref>
Cardiac amyloid cab be associated with the following symptoms:<ref name="pmid9578896">{{cite journal |author=Dubrey SW, Cha K, Anderson J, ''et al.'' |title=The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement |journal=[[QJM : Monthly Journal of the Association of Physicians]] |volume=91 |issue=2 |pages=141–57 |year=1998 |month=February |pmid=9578896 |doi= |url=}}</ref>
*[[Congestive heart failure]] such as  
*[[Congestive heart failure]] with associated symptoms such as  
**[[Fatigue]]
**[[Fatigue]]
** [[Dyspnea]]
** [[Dyspnea]]

Revision as of 20:10, 29 October 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]; Aarti Narayan, M.B.B.S [3]; Cafer Zorkun, M.D., Ph.D. [4]; Lakshmi Gopalakrishnan, M.B.B.S. [5]

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Overview

Amyloidosis is a multi-system disease involving many organs simultaneously. Approximately more than 50% of the patients with amyloidosis present with right heart failure symptoms. The most common symptoms observed in patients with cardiac amyloidosis include fatigue, weight loss, and periorbital purpura.[1]

Symptoms

Cardiac amyloid cab be associated with the following symptoms:[2]

References

  1. 1.0 1.1 Kyle RA, Gertz MA (1995). "Primary systemic amyloidosis: clinical and laboratory features in 474 cases". Seminars in Hematology. 32 (1): 45–59. PMID 7878478. Unknown parameter |month= ignored (help); |access-date= requires |url= (help)
  2. Dubrey SW, Cha K, Anderson J; et al. (1998). "The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement". QJM : Monthly Journal of the Association of Physicians. 91 (2): 141–57. PMID 9578896. Unknown parameter |month= ignored (help)
  3. Mugnai G, Cicoira M, Rossi A, Vassanelli C (2011). "Syncope in cardiac amyloidosis and chronic ischemic heart disease: A case report". Experimental and Clinical Cardiology. 16 (2): 51–3. PMC 3126684. PMID 21747665.
  4. Rapezzi C, Perugini E, Salvi F, Grigioni F, Riva L, Cooke RM, Ferlini A, Rimessi P, Bacchi-Reggiani L, Ciliberti P, Pastorelli F, Leone O, Bartolomei I, Pinna AD, Arpesella G, Branzi A (2006). "Phenotypic and genotypic heterogeneity in transthyretin-related cardiac amyloidosis: towards tailoring of therapeutic strategies?". Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 13 (3): 143–53. doi:10.1080/13506120600877136. PMID 17062380. Retrieved 2012-02-13. Unknown parameter |month= ignored (help)
  5. Mueller PS, Edwards WD, Gertz MA (2000). "Symptomatic ischemic heart disease resulting from obstructive intramural coronary amyloidosis". The American Journal of Medicine. 109 (3): 181–8. PMID 10974179. Unknown parameter |month= ignored (help)
  6. Al Suwaidi J, Velianou JL, Gertz MA; et al. (1999). "Systemic amyloidosis presenting with angina pectoris". Annals of Internal Medicine. 131 (11): 838–41. PMID 10610629. Unknown parameter |month= ignored (help)


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