心アミロイドーシス
WordNet
- of or relating to the heart; "cardiac arrest"
- a disorder characterized by deposit of amyloid in organs or tissues; often secondary to chronic rheumatoid arthritis or tuberculosis or multiple myeloma
- the opening into the stomach and that part of the stomach connected to the esophagus
PrepTutorEJDIC
- 心臓の
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2012/08/07 21:03:19」(JST)
[Wiki en表示]
Cardiac amyloidosis may refer to:
- Cardiac manifestations of AL amyloidosis
- Cardiac manifestations of transthyretin-related hereditary amyloidosis
- Isolated atrial amyloidosis
UpToDate Contents
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English Journal
- Diagnostic and prognostic value of subcutaneous tissue biopsy in patients with cardiac amyloidosis.
- Takashio S, Izumiya Y, Jinnin M, Yamamuro M, Kojima S, Ihn H, Ogawa H.SourceDepartment of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
- The American journal of cardiology.Am J Cardiol.2012 Nov 15;110(10):1507-11. doi: 10.1016/j.amjcard.2012.06.059. Epub 2012 Aug 3.
- Cardiac involvement in systemic amyloidosis causes detrimental prognosis; therefore, early detection and classification are important to develop appropriate therapeutic strategies. Subcutaneous tissue biopsy is a useful screening procedure for systemic amyloidosis; however, its diagnostic and progno
- PMID 22863178
- Familial Mediterranean fever: New phenotypes.
- Soriano A, Manna R.SourcePeriodic Fever Research Centre, National Reference Centre for FMF, Catholic University of the Sacred Heart, Rome, Italy.
- Autoimmunity reviews.Autoimmun Rev.2012 Nov;12(1):31-7. doi: 10.1016/j.autrev.2012.07.019. Epub 2012 Aug 2.
- Familial Mediterranean fever (FMF) is an inherited autosomal recessive disorder, ethnically restricted and commonly found among individuals of Mediterranean descent, caused by MEditerranean FeVer gene (MEFV) mutations on chromosome 16. It is the most frequent periodic febrile syndrome among the auto
- PMID 22878273
Japanese Journal
- Erratum: Novel method for quantitative evaluation of cardiac amyloidosis using 201TlCl and 99mTc-PYP SPECT (Annals of Nuclear Medicine (2012) DOI: 10.1007/s12149-012-0627-y)
- Yamamoto Yasushi,Onoguchi Masahisa,Haramoto Masuo,Kodani Nobuhiro,Komatsu Akio,Kitagaki Hajime,Tanabe Kazuaki
- Erratum: Novel method for quantitative evaluation of cardiac
- NAID 120005253224
- Novel method for quantitative evaluation of cardiac amyloidosis using ^<201>TlCl and ^<99m>Tc-PYP SPECT
- YAMAMOTO Yasushi,ONOGUCHI Masahisa,HARAMOTO Masuo,KODANI Nobuhiro,KOMATSU Akio,KITAGAKI Hajime,TANABE Kazuaki
- Annals of nuclear medicine 26(8), 634-643, 2012-10-01
- NAID 10031126412
Related Links
- Echocardiogram Magnetic resonance imaging (MRI) Nuclear heart scans (MUGA, RNV) An ECG may show problems with the heart beat or heart signals (conduction disturbance). A cardiac biopsy is used to confirm the diagnosis. A ...
- Case presentation: A 55-year-old woman, who had previously been very physically active, noted a gradual decrease in exercise tolerance over a period of 3 to 4 months to the extent that she had to rest briefly after ...
Related Pictures
★リンクテーブル★
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- 英
- cardiac amyloidosis
- 同
- 心アミロイド症
- 関
- アミロイドーシス
病理
- 肉眼 :心房内膜に小結節を認める
- 顕微鏡:アミロイドの間質への沈着。アミロイドによる心筋細胞の圧排。アミロイドによる心筋細胞の消失。 → つまり、心筋間質の硬化と心筋細胞の萎縮
検査
心電図
- 低電位、異常Q波、上室性不整脈(心房細動)、伝導障害、(左室収縮障害が著明な場合)電気的交互脈 (ECGP.359)
- 前胸部誘導のQS、肢誘導低電位、伝導障害
心エコー
- 左室壁のびまん性肥厚。内腔は正常かやや増加。左房拡大(←拘束性心筋症の特徴?)。(ECGP.359)
病態
- まとめると拘束性障害と伝導障害
- 低心拍出
- 心不全 ← ジギタリス無効。ジギタリス中毒をきたしやすい。(腎機能が低下していることが多いから?)
- 伝導障害
- 心筋肥大
症状
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- 関
- cardio、cardiotonic、heart、mind
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アミロイドーシス アミロイド症