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==Historical Perspective==
==Historical Perspective==
*In 1954, Lenègre published the condition in French, hence, it is also referred to as Lenègre’s disease or Maladie de Lenègre in French, after his name.<ref name="pmid14153648">{{cite journal| author=LENEGRE J| title=ETIOLOGY AND PATHOLOGY OF BILATERAL BUNDLE BRANCH BLOCK IN RELATION TO COMPLETE HEART BLOCK. | journal=Prog Cardiovasc Dis | year= 1964 | volume= 6 | issue=  | pages= 409-44 | pmid=14153648 | doi=10.1016/s0033-0620(64)80001-3 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14153648  }} </ref>
*In 1954, Lenègre published the condition in French, hence, it is also referred to as Lenègre’s disease or Maladie de Lenègre in French, after his name.<ref name="pmid14153648">{{cite journal| author=LENEGRE J| title=ETIOLOGY AND PATHOLOGY OF BILATERAL BUNDLE BRANCH BLOCK IN RELATION TO COMPLETE HEART BLOCK. | journal=Prog Cardiovasc Dis | year= 1964 | volume= 6 | issue=  | pages= 409-44 | pmid=14153648 | doi=10.1016/s0033-0620(64)80001-3 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14153648  }} </ref>
*In 1964, it was described independently by the two researchers, Jean Lenègre and Maurice Lev in English, but the condition is generally called after Lev.<ref>Lev M. ''Anatomic basis for atrioventricular block''. Am J Med 1964;37:742-8. PMID 14237429.</ref><ref>Lenegre J. ''Etiology and pathology of bilateral bundle branch block in relation to complete heart block.'' Prog Cardiovasc Dis 1964;6:409-444. PMID 14153648.</ref><ref name="pmid14237429">{{cite journal| author=LEV M| title=ANATOMIC BASIS FOR ATRIOVENTRICULAR BLOCK. | journal=Am J Med | year= 1964 | volume= 37 | issue=  | pages= 742-8 | pmid=14237429 | doi=10.1016/0002-9343(64)90022-1 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14237429  }} </ref><ref>https://annals.org/aim/article-abstract/696353/lev-len-gre-diseases</ref>
*In 1964, it was described independently by the two researchers, Jean Lenègre and Maurice Lev in English, but the condition is generally called after Lev.<ref>Lev M. ''Anatomic basis for atrioventricular block''. Am J Med 1964;37:742-8. PMID 14237429.</ref><ref>Lenegre J. ''Etiology and pathology of bilateral bundle branch block in relation to complete heart block.'' Prog Cardiovasc Dis 1964;6:409-444. PMID 14153648.</ref><ref name="pmid14237429">{{cite journal| author=LEV M| title=ANATOMIC BASIS FOR ATRIOVENTRICULAR BLOCK. | journal=Am J Med | year= 1964 | volume= 37 | issue=  | pages= 742-8 | pmid=14237429 | doi=10.1016/0002-9343(64)90022-1 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14237429  }} </ref><ref>https://annals.org/aim/article-abstract/696353/lev-len-gre-diseases</ref><ref name="pmid30723001">{{cite journal| author=Carius BM, Long B, Schauer S| title=Lev's Syndrome: A rare case of progressive cardiac conduction disorder presenting to the emergency department. | journal=Am J Emerg Med | year= 2019 | volume= 37 | issue= 5 | pages= 1006.e1-1006.e4 | pmid=30723001 | doi=10.1016/j.ajem.2019.01.054 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30723001  }} </ref>


==Pathophysiology==
==Pathophysiology==

Revision as of 21:04, 17 August 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Sara Mohsin, M.D.[2]

Synonyms and keywords: Lenègre-Lev disease, Lenègre’s disease, Maladie de Lenègre, Acquired complete heart block

Overview

Lev's disease is an acquired complete heart block due to idiopathic fibrosis and calcification of the electrical conduction system of the heart. Lev's disease is most commonly seen in the elderly and is often described as senile degeneration of the conduction system.

One form has been associated with SCN5A. Lev's Syndrome is a rare, progressive cardiac conduction defect (PCCD) due to myocardial fibrosis first described by Maurice Lev in 1964. This condition, proposed to start in the fourth decade of life, involves a sclerotic fibro-fatty degeneration of the Bundle of His and Purkinje fibers, which Lev proposed caused increasing AV delay with age. With the prevalence of electrocardiogram (ECG) use in the emergency department (ED) for cardiac- and non-cardiac complaints, dysrhythmias can be incidentally found and confuse diagnosis and disposition. We highlight the case of an 84-year-old male who presented to the ED for acute onset of diffuse facial paresthesias with elevated blood pressure at home and was found to be significantly bradycardic on initial evaluation. On serial ECGs, the conduction rhythm changed from an initial new first-degree atrioventricular (AV) block with left bundle branch block (LBBB), to a later first-degree AV block without LBBB. Cardiology was consulted. Serial ECGs demonstrated an evolving conduction block arrhythmia consistent with Lev's Syndrome. Here we describe a case of symptomatic bradycardia found to be consistent with Lev's Syndrome.

Historical Perspective

  • In 1954, Lenègre published the condition in French, hence, it is also referred to as Lenègre’s disease or Maladie de Lenègre in French, after his name.[1]
  • In 1964, it was described independently by the two researchers, Jean Lenègre and Maurice Lev in English, but the condition is generally called after Lev.[2][3][4][5][6]

Pathophysiology

One form has been associated with SCN5A[7]

  • Fibrous transformation progressive and slow, of degenerative origin, of the two branches of the bundle of His, resulting in progressive conductional disorders:[8][9][10][11][12][13]
    • block of branch with or without hemibloc of the opposite side
    • then complete, paroxysmal then permanent block of auriculoventricular (disease of Adams-Stokes).

Associated Conditions

Stokes-Adams attacks can be precipitated by this condition. These involve a temporary loss of consciousness due to ventricular fibrillation or asystole.[6]

Pathophysiology of AV Block

  • Fibrosis and sclerosis of the conduction system, which appears idiopathic, accounts for about one-half of cases of AV block.
  • Conduction system fibrosis and sclerosis may be induced by several different conditions that often cannot be distinguished clinically.
  • Additionally, some degree of fibrosis and sclerosis occurs as part of the normal aging process, with the prevalence increasing progressively with age with approximately a 2:1 male:female predominance.
  • Among a prospective cohort of more than half a million United Kingdom residents, the prevalence of conduction system disease (which included all levels of AV block, as well as bundle branch blocks) was approximately 11 per 10,000 persons under age 55 and increased to between 55 per 10,000 persons ≥65 years of age.
  • Idiopathic — Apparently idiopathic progressive cardiac conduction defects are the most common cause of AV block, occurring in approximately 50 percent of cases. Idiopathic AV conduction abnormalities are characterized by progressive impairment of the conduction system which occurs gradually over decades:

●Lenegre's disease – The term Lenegre's disease has been traditionally used to describe a progressive, fibrotic, sclerodegenerative affliction of the conduction system in younger (age <60 years) individuals. Lenegre's disease is frequently associated with slow progression to complete heart block and may be hereditary.

●Lev's disease – The term Lev's disease has been used to refer to "sclerosis of the left side of the cardiac skeleton" in older patients (age >70 years old), such as that associated with calcific involvement of the aortic and mitral rings. Lev's disease is caused by fibrosis or calcification extending from any of the fibrous structures adjacent to the conduction system into the conduction system.[1][4][14][15][16][17][18][19][20][21]

Depending upon the anatomic location of the areas of fibrosis and sclerosis, various conduction abnormalities can result with the following causing Lev's disease:

●Involvement of the mitral ring or the central fibrous body, for example, may be the most common cause of complete heart block with a narrow QRS complex in the elderly.

Related Chapters

References

  1. 1.0 1.1 LENEGRE J (1964). "ETIOLOGY AND PATHOLOGY OF BILATERAL BUNDLE BRANCH BLOCK IN RELATION TO COMPLETE HEART BLOCK". Prog Cardiovasc Dis. 6: 409–44. doi:10.1016/s0033-0620(64)80001-3. PMID 14153648.
  2. Lev M. Anatomic basis for atrioventricular block. Am J Med 1964;37:742-8. PMID 14237429.
  3. Lenegre J. Etiology and pathology of bilateral bundle branch block in relation to complete heart block. Prog Cardiovasc Dis 1964;6:409-444. PMID 14153648.
  4. 4.0 4.1 LEV M (1964). "ANATOMIC BASIS FOR ATRIOVENTRICULAR BLOCK". Am J Med. 37: 742–8. doi:10.1016/0002-9343(64)90022-1. PMID 14237429.
  5. https://annals.org/aim/article-abstract/696353/lev-len-gre-diseases
  6. 6.0 6.1 Carius BM, Long B, Schauer S (2019). "Lev's Syndrome: A rare case of progressive cardiac conduction disorder presenting to the emergency department". Am J Emerg Med. 37 (5): 1006.e1–1006.e4. doi:10.1016/j.ajem.2019.01.054. PMID 30723001.
  7. Schott JJ, Alshinawi C, Kyndt F; et al. (1999). "Cardiac conduction defects associate with mutations in SCN5A". Nat. Genet. 23 (1): 20–1. doi:10.1038/12618. PMID 10471492.
  8. https://litfl.com/lenegre-lev-disease/
  9. https://academic.oup.com/europace/article/7/2/122/557245
  10. Mueller, Richard L.; Bergman, Geoffrey (1995). "Calcific Aortic Stenosis and Associated Lev's Disease". Circulation. 92 (10): 3138–3138. doi:10.1161/01.CIR.92.10.3138. ISSN 0009-7322.
  11. Royer, Anne; van Veen, Toon A.B.; Le Bouter, Sabrina; Marionneau, Céline; Griol-Charhbili, Violaine; Léoni, Anne-Laure; Steenman, Marja; van Rijen, Harold V.M.; Demolombe, Sophie; Goddard, Catharine A.; Richer, Christine; Escoubet, Brigitte; Jarry-Guichard, Thérèse; Colledge, William H.; Gros, Daniel; de Bakker, Jacques M.T.; Grace, Andrew A.; Escande, Denis; Charpentier, Flavien (2005). "Mouse Model of SCN5A -Linked Hereditary Lenègre's Disease". Circulation. 111 (14): 1738–1746. doi:10.1161/01.CIR.0000160853.19867.61. ISSN 0009-7322. line feed character in |title= at position 15 (help)
  12. Okada R (1996). "[Lev's disease]". Ryoikibetsu Shokogun Shirizu (15): 515–8. PMID 9048083.
  13. Suzuki H, Kawai S (1996). "[Lenegre's disease]". Ryoikibetsu Shokogun Shirizu (15): 512–4. PMID 9048082.
  14. LEV M (1964). "THE PATHOLOGY OF COMPLETE ATRIOVENTRICULAR BLOCK". Prog Cardiovasc Dis. 6: 317–26. doi:10.1016/s0033-0620(64)80005-0. PMID 14105712.
  15. Altunkaş F, Onalan O, Bekar L, Ceyhan K (2010). "E-page original images. Lev's disease: insidious enemy of conduction system". Anadolu Kardiyol Derg. 10 (6): E25. doi:10.5152/akd.2010.176. PMID 21062696.
  16. Mueller RL, Bergman G (1995). "Images in cardiovascular medicine. Calcific aortic stenosis and associated Lev's disease". Circulation. 92 (10): 3138. doi:10.1161/01.cir.92.10.3138. PMID 7586286.
  17. Kushakovskiĭ MS, Baliabin AA, Uspenskaia MK (1991). "[Chronic idiopathic bundle-branch block. Lenegre's and Lev's diseases]". Kardiologiia. 31 (8): 99–103. PMID 1795490.
  18. Stéphan E, Aftimos G, Allam C (1985). "Familial fascicular block: histologic features of Lev's disease". Am Heart J. 109 (6): 1399–401. doi:10.1016/0002-8703(85)90377-1. PMID 4003252.
  19. Rasmussen KS, Paulsen SM (1980). "[Total atrioventricular block caused by dystrophic calcification: Lev's disease]". Ugeskr Laeger. 142 (45): 2986–7. PMID 7466946.
  20. Cupp GV, Watson LE, Martin RH (1975). "Concealed conduction in a case of Lev's disease. Case report". Mo Med. 72 (4): 189–91, 193. PMID 1128498.
  21. Ramírez A, Dumont CR, Medrano GA, Testelli M, Hurtado L (1974). "[Lev's disease. Report of a case]". Arch Inst Cardiol Mex. 44 (6): 894–901. PMID 4441160.


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