icon fsr

文献詳細

雑誌文献

循環器ジャーナル70巻1号

2022年01月発行

文献概要

特集 心筋症診療のフロントライン—概念から最新の治療まで Ⅲ章 病理

心筋症の病理

著者: 池田善彦1

所属機関: 1国立循環器病研究センター病理部病理診断科

ページ範囲:P.23 - P.32

文献購入ページに移動
Point
・心筋炎の中では,ステロイドや免疫抑制療法が有効な好酸球性,巨細胞性,肉芽腫性,ループス心筋炎の診断は重要である.心筋炎疑診例での凍結組織を用いた迅速診断は有用である.
・二次性心筋症の診断には,PAS,diastase PAS,oil red O,酸ホスファターゼなどの特殊染色,Gb3,LAMP 2,ATGL,PLIN 2,AL-κ,AL-λ,ATTR,AA,dystrophinⅠ・Ⅱ・Ⅲ,dystrophin A・B,PD-L1,ubiquitinなどの免疫染色,電顕による検索が有用である.

参考文献

1)Watkins H, McKenna W, Thierfelder L, et al : Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy. N Engl J Med 332 : 1058-1064, 1995
2)Varnava AM, Elliott PM, Baboonian C, et al : Hypertrophic cardiomyopathy : histopathological features of sudden death in cardiac troponin T disease. Circulation 104 : 1380-1384, 2001
3)Pilichou K, Nava A, Basso C, et al : Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy. Circulation 113 : 1171-1179, 2006
4)Rampazzo A, Nava A, Malacrida S, et al : Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet 71 : 1200-1206, 2002
5)Gerull B, Heuser A, Wichter T, et al : Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy. Nat Genet 36 : 1162-1164, 2004
6)van Tintelen JP, Entius MM, Bhuiyan ZA, et al : Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation 113 : 1650-1658, 2006
7)Wright BL, Leiferman KM, Gleich GJ : Eosinophil granule protein localization in eosinophilic endomyocardial disease. N Engl J Med 365 : 187-188, 2011
8)Aretz HT : Myocarditis, granulomatous. In : Bloom S, ed. Diagnostic criteria for cardiovascular pathology : Acquired Diseases. p73, Lippincott Williams & Wilkins, Philadelphia, 1997
9)Weidemann F, Niemann M, Breunig F, et al : Long-term effects of enzyme replacement therapy on Fabry cardiomyopathy : Evidence for a better outcome with early treatment. Circulation 119 : 524-529, 2009
10)Apelland T, Gude E, Strøm EH, et al : Familial globotriaosylceramide-associated cardiomyopathy mimicking Fabry disease. Heart 100 : 1793-1798, 2014
11)Danon MJ, Oh SJ, DiMauro S, et al : Lysosomal glycogen storage disease with normal acid maltase. Neurology 31 : 51-57, 1981
12)Nishino I, Fu J, Tanji K, et al : Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy(Danon disease). Nature 406 : 906-910, 2000
13)Hirano K, Ikeda Y, Zaima N, et al : Triglyceride deposit cardiomyovasculopathy. N Engl J Med 359 : 2396-2398, 2008
14)Ikeda Y, Hirano K, Fukushima N, et al : A novel type of human spontaneous coronary atherosclerosis with triglyceride deposition. Eur Heart J 35 : 875, 2014
15)Hirano K, Ikeda Y, Sugimura K, et al : Cardiomyocyte steatosis and defective washout of iodine-123-β-methyl iodophenyl-pentadecanoic acid in genetic deficiency of adipose triglyceride lipase. Eur Heart J 36 : 580, 2015
16)Jordans GH : The familial occurrence of fat containing vacuoles in the leucocytes diagnosed in two brothers suffering from dystrophia musculorum progressiva. Acta Med Scand 145 : 419-423, 1953
17)Li M, Hirano K, Ikeda Y, et al : Triglyceride deposit cardiomyovasculopathy : a rare cardiovascular disorder. Orphanet J Rare Dis 14 : 134, 2019
18)Bristow MR, Billingham ME, Mason JW, et al : Clinical spectrum of anthracycline antibiotic cardiotoxicity. Cancer Treat Rep 62 : 873-879, 1978
19)Virmani R, Burke A, Farb A : Endomyocardial biopsy in the nontransplant setting. In : Atlas of cardiovascular pathology. WB Saunders, Philadelphia, 1996

掲載誌情報

出版社:株式会社医学書院

電子版ISSN:2432-3292

印刷版ISSN:2432-3284

雑誌購入ページに移動
icon up
あなたは医療従事者ですか?