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C. Iordache

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Articole semnate de acelasi autor in Revista Romana de Pediatrie:

Bland-White-Garland syndrome with early fatal evolution

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Revista Romana de PEDIATRIE | Volumul LXI, Nr. 3, An 2012
ISSN 1454-0398  |  e-ISSN 2069-6175
ISSN-L 1454-0398
DOI: 10.37897/RJP

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Bland-White-Garland syndrome with early fatal evolution

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ABSTRACT

The authors present the case of an 2 months old infant, who is hospitalized for clinical signs of congestive heart failure, with dilated cardiomyopathy on Doppler echocardiography and myocardial infarction on ECG. Despite the medical treatment the evolution was unfavorable, and pathological examination confirms the anomalous origin of the left coronary artery (LCA) from the pulmonary artery (PA), dilated left ventricular cardiomyopathy, secondary subendocardic fibroelastosis and necrosis.

Key words: anomalous origin of the left coronary artery, heart failure, dilated cardiomyopathy, myiocardial ischemia

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SINDROM BLAND-WHITE-GARLAND CU EVOLUTIE FATALA PRECOCE

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Revista Romana de PEDIATRIE | Volumul LXI, Nr. 3, An 2012
ISSN 1454-0398  |  e-ISSN 2069-6175
ISSN-L 1454-0398
DOI: 10.37897/RJP

Indexed

DOI - Crossref
Similarity Check by iThenticate, worldwide No 1 professional plagiarism checking system
DOAJ
Scopus
NLM Catalog
Ebsco Host - Medline
Google Academic
Semantic Scholar

HIGHLIGHTS

National Awards “Science and Research”

NEW! RJP has announced the annually National Award for "Science and Research" for the best scientific articles published throughout the year in the official journal.

ICMJE- Recommendations

Read the Recommendations for the Conduct, Reporting, Editing, and Publication of Scholarly work in Medical Journals.

Promoting Global Health

The published medical research literature is a global public good. Medical journal editors have a social responsibility to promote global health by publishing, whenever possible, research that furthers health worldwide.

SINDROM BLAND-WHITE-GARLAND CU EVOLUTIE FATALA PRECOCE

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REZUMAT

Autorii prezintă cazul unui sugar în vârstă se 2 luni, care se internează pentru semne clinice de insuficienţă cardiacă congestivă ce asociază hipotensiune arterială şi timp de recolorare prelungit, cu cardiomiopatie dilatativă la ecocardiografia Doppler şi modificări ischemice pe EKG. În ciuda tratamentului medicamentos, evoluţia a fost nefavorabilă, iar examenul anatomopatologic confirmă originea anormală a arterei coronare stângi (ACS) din artera pulmonară (AP), cardiomiopatia dilatativă a ventriculului stâng şi evidenţiază fibroelastoză şi necroză subendocardică secundare.

Cuvinte cheie: origine anormală a arterei coronare stângi, insuficienţă cardiacă, cardiomiopatie dilatativă, ischemie miocardică

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