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Spontaneous pericardial hematoma with familial amyloid polyneuropathy.

Authors :
Nakanishi N
Sawada T
Sato R
Yanishi K
Akakabe Y
Nishizawa S
Kuroyanagi A
Tsubakimoto Y
Matsui A
Nakamura T
Shiraishi H
Matsumuro A
Shirayama T
Matsubara H
Source :
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis [Amyloid] 2009 Dec; Vol. 16 (4), pp. 221-5.
Publication Year :
2009

Abstract

There are more than a few risks of hemorrhage complication in patients with amyloidosis. Although most cases with amyloidosis exhibit minor bleeding manifestations, they can be occasionally associated with life-threatening problems. To our knowledge, there are only a few cases of spontaneous pericardial hematoma associated with amyloidosis. We here report a patient who suddenly died of cardiac tamponade with massive pericardial hematoma 7 years after the diagnosis of familial amyloid polyneuropathy (FAP). A 69-year-old female with FAP with cardiogenic shock was admitted to our emergency room. Although she previously underwent permanent pacemaker implantation for atrial fibrillation with slow ventricular response, electrocardiogram showed a critical pacing failure. Emergent telemetry check revealed a sudden extreme increase of pacing capture threshold in the right ventricle. Maximum pacing voltage could not improve the critical condition, and she died 7 h after arrival. Autopsy showed a massive pericardial hematoma in the right ventricular free wall, and microscopic examination revealed typical amyloid deposition in the arterial wall of the pericardium. In this case, it is assumed that a sudden rupture of fragile pericardial vessels with amyloid deposition led to the lethal pericardial hematoma.

Details

Language :
English
ISSN :
1744-2818
Volume :
16
Issue :
4
Database :
MEDLINE
Journal :
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Publication Type :
Academic Journal
Accession number :
19922334
Full Text :
https://doi.org/10.3109/13506120903421751