Autor: |
M, Puyade, J, Badin, B, Quéron, L, Christiaens, N, Varroud-Vial, F, Pierre, O, Pourrat |
Jazyk: |
francouzština |
Rok vydání: |
2012 |
Předmět: |
|
Zdroj: |
La Revue de medecine interne. 35(4) |
ISSN: |
1768-3122 |
Popis: |
Thrombotic thrombocytopenic purpura (TTP) is a thrombotic microangiopathy due to ADAMTS13 deficiency (a von Willebrand factor's metalloprotease) with multiple organs' involvement, one of which may be the heart.We report a 29-year-old woman who presented a TTP during her last trimester of pregnancy, under the features of a HELLP syndrome. After caesarean section, cardiac involvement was revealed by chest pain, ECG changes, antero-septal hypokinesia and troponin rise. Cardiac MRI found no large-vessel ischemic heart disease and confirmed hypokinesia.When TTP is diagnosed, cardiac involvement must be systematically investigated by ECG and troponin assay because of the risk of a cardiac arrest. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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