Situs inversus with dextrocardia in a mummy case

被引：6

作者：

Zanatta, Alberto ^{[1
]}

Zampieri, Fabio ^{[1
]}

Bonati, Maurizio Rippa ^{[1
]}

Frescura, Carla ^{[1
]}

Scattolin, Giuliano ^{[2
]}

Stramare, Roberto ^{[2
]}

Thiene, Gaetano ^{[1
]}

机构：

[1] Univ Padua, Sch Med, Dept Cardiac Thorac & Vasc Sci, I-35100 Padua, Italy

[2] Univ Padua, Sch Med, Dept Med, I-35100 Padua, Italy

来源：

CARDIOVASCULAR PATHOLOGY | 2014年 / 23卷 / 01期

关键词：

Dextrocardia; Mummy; Situs inversus; Ventricular septal defect; DIAGNOSIS;

D O I：

10.1016/j.carpath.2013.07.002

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

A mummy of a young woman, who died due to tuberculous peritonitis and salpingitis, is conserved in the Pathological Anatomy Museum of the University of Padua. It was found at autopsy to have situs inversus of viscera with dextrocardia, apparently in the absence of other congenital defects. A 64-section scanner computed tomography (CT) on the specimen was carried out to investigate the internal condition of organs. The CT revealed the presence in the heart of a muscular ventricular septal defect and of calcific deposits on visceral pericardium and aortic wall, in keeping with sequelae of previous tuberculous pericarditis. (C) 2014 Elsevier Inc. All rights reserved.

引用

页码：61 / 64

页数：4

共 25 条

[1] Adarsh K, 2005, J INDIAN ACAD MED, V27, P122
[2] AFZELIUS BA, 1981, AM J HUM GENET, V33, P852
[3] ANSELMI G, 1972, BRIT HEART J, V34, P1085
[4] Baillie M., 1788, PHILOS T R SOC LOND, V78, P350, DOI [10.1098/rstl.1788.0023, DOI 10.1098/RSTL.1788.0023]
[5] Heterotaxia, congenital heart disease, and primary ciliary dyskinesia
Brueckner, Martina
[J]. CIRCULATION, 2007, 115 (22) : 2793 - 2795
[6] Brunetti L., 1878, SCUOLA ANATOMIA PATO, P79
[7] Brunetti L., 1876, NOTICE NOUVELLE METH, P32
[8] Difficulties for cardiovascular retrospective diagnosis on mummified foetal remains
Charlier, Philippe
Huynh-Charlier, Isabelle
[J]. CARDIOLOGY IN THE YOUNG, 2013, 23 (03) : 470 - 471
[9] De Tommasi S M, 1980, G Ital Cardiol, V10, P1192
[10] Loeys-Dietz syndrome: A possible solution for Akhenaten's and his family's mystery syndrome
Eshraghian, Ahad
Loeys, Bart
[J]. SAMJ SOUTH AFRICAN MEDICAL JOURNAL, 2012, 102 (08): : 661 - 664

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