Fulminant apical ballooning syndrome after replacement of a prosthetic aortic valve.

Gen Thorac Cardiovasc Surg

Department of Cardiovascular Surgery, KKR Sapporo Medical Center, Hiragishi 1-6, Toyohira-ku, Sapporo, Hokkaido, 062-0931, Japan.

Published: September 2009

A 70-year-old woman was readmitted to our hospital with a fever of 39 degrees C on the 30th day after replacement of a prosthetic aortic valve. She required percutaneous cardiopulmonary support for her heart failure and was weaned after 7 days. Echocardiography revealed an akinetic and aneurysmally dilated left ventricular apex and hyperdynamic basal segments. This case indicates that fulminant apical ballooning syndrome might be added to the list of potential complications after cardiac surgery.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11748-009-0414-4DOI Listing

Publication Analysis

Top Keywords

fulminant apical
8
apical ballooning
8
ballooning syndrome
8
replacement prosthetic
8
prosthetic aortic
8
aortic valve
8
syndrome replacement
4
valve 70-year-old
4
70-year-old woman
4
woman readmitted
4

Similar Publications

Background: Fulminant eosinophilic myocarditis (EM) is a rare and often fatal condition that may present atypically and be complicated by ventricular arrhythmias. Treatment involves high-dose corticosteroids to suppress eosinophilia, as well as increasing use of mepolizumab, an anti-interleukin-5 antibody with evidence for long-term efficacy and safety.

Case Summary: A 38-year-old woman presented to the emergency department with neck pain and fatigue, and after extensive investigation was diagnosed with EM secondary to idiopathic hypereosinophilic syndrome.

View Article and Find Full Text PDF
Article Synopsis
  • Hypereosinophilia (HE) is characterized by an eosinophil count over 1500 cells/microL in blood tests, confirmed by either blood tests or high eosinophil percentages in bone marrow samples. Hypereosinophilic syndrome (HES) involves organ damage due to eosinophils and can be classified as primary, secondary, or idiopathic.
  • Cardiac issues occur in 5% of acute cases and 20% of chronic cases of HES, presenting symptoms like heart failure and arrhythmias, but the severity of heart problems isn't always proportional to eosinophil levels.
  • Diagnosis of cardiac involvement relies on advanced imaging techniques, particularly
View Article and Find Full Text PDF

Sialidosis is an ultra-rare multisystemic lysosomal disease caused by mutations in the neuraminidase 1 (NEU1) gene. The severe type II form of the disease manifests with a prenatal/infantile or juvenile onset, bone abnormalities, severe neuropathology, and visceromegaly. A subset of these patients present with nephrosialidosis, characterized by abrupt onset of fulminant glomerular nephropathy.

View Article and Find Full Text PDF

Recurrent giant cell myocarditis after heart transplant: a case report.

Eur Heart J Case Rep

September 2022

Division of Cardiology, Jefferson Heart Institute, Sidney Kimmel School of Medicine, Thomas Jefferson University Hospital, 925 Chestnut Street, Suite 200, Philadelphia, PA 19107, USA.

Article Synopsis
  • Giant cell myocarditis (GCM) is a rare but severe form of myocarditis that can lead to heart failure and often requires a heart transplant for treatment.
  • A 33-year-old man with worsening heart function was diagnosed with GCM after initially being discharged on medication; he ultimately needed a heart transplant due to the disease's progression.
  • Post-transplant, he experienced recurrent GCM and required intensified immunosuppressive therapy, which resulted in several infections, but as of the latest follow-up, he is stable.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!