A case of systemic AL amyloidosis identified by autopsy with suspected epicardial amyloid deposits on echocardiography-Reference-Cited by-同舟云学术

A case of systemic AL amyloidosis identified by autopsy with suspected epicardial amyloid deposits on echocardiography

Published:2022 Issue:1 Volume:49 Page:39-49
ISSN:1346-1176
Container-title:Choonpa Igaku
language:en
Short-container-title:Jpn J Med Ultrasonics

Author:

CHIBA Mio¹,TATEISHI Ryo²,TOKURA Taichiro³,MISU Yoshiki²,KOJIMA Yui⁴,NISHIGOORI Shuhei⁵,NAKAYAMA Kazutaka³,FUJII Hiroyuki²

Affiliation:

1. Department of Clinical Laboratory, Yokohama Minami Kyousai Hospital

2. Department of Cardiology, Yokohama Minami Kyousai Hospital

3. Department of Hematology, Yokohama Minami Kyousai Hospital

4. Department of Pathology, Yokohama Minami Kyousai Hospital

5. Department of Gastrointestinal, Yokohama Minami Kyousai Hospital

Publisher

Japan Society of Ultrasonics in Medicine

Subject

Radiology, Nuclear Medicine and imaging

Link

https://www.jstage.jst.go.jp/article/jjmu/49/1/49_JJMU.A.205/_pdf

Reference21 articles.

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2. 2) Benson MD, Buxbaum JN, Eisenberg DS, et al. Amyloid nomenclature 2018: recommendations by the International Society of Amyloidosis (ISA) nomenclature committee. Amyloid. 2018;25:215-9.

3. 3) 茶谷絵理．プログラミングされていないフォールディング-アミロイド線維の形成．生化学．2015;87:292-7.

4. 4) Dubrey SW, Cha K, Anderson J, et al. The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement. QJM.1998;91:141-57.

5. 5) Ridolfi RL, Bulkley BH, Hutchins GM. The conduction system in cardiac amyloidosis: clinical and pathologic features of 23 patients. Am J Med. 1977;62:677-86.