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A Case Report of Case Report Pursuit by Medical Student
Medical students often seek case reports as vehicles for academic writing opportunities, conference presentation avenues, and residency/fellowship application highlights. Here we review a case where, due to unfortunate circumstances, a student made a unique diagnosis central to proper patient clinical care, wished to write up the case subsequently, but was ultimately excluded from the final work stemming from the patient case. We review the pitfalls that occurred in the process of pursuing publication of an interesting case, the educational value of pursuing case reports for students, the necessity for strong mentorship in this process, and general principles that medical students can follow regarding case report creation to avoid being burned
Case Reports
Abstracts of the 12th Indonesian Society of Interventional Cardiology Annual Meeting (ISICAM) 2020
27-29 November 202
Case Reports
Abstracts of the 5th InaPrevent in Conjunction with the 1st InTension Summit, 25-27 June 202
Case Reports
Indonesian Society of Interventional Cardiology Annual Meeting 2021
Abstracts: Case Report
Case Reports
Abstracts of the 29th Annual Scientific Meeting of the Indonesian Heart Association (ASMIHA)
1st ASMIHA Digital Conference, 23-25 October 202
Case reports
Whether to a greater or lesser extent, genetics often plays an important role in the development
of cardiovascular diseases. Here we report a newly identified family with familial coronary
artery disease (CAD) and left ventricular non-compaction (LVNC).
A 52-year-old male with acute coronary syndrome, in whom LVNC had been found "incidentally",
was admitted for revascularisation. From a two-dimensional echocardiogram the epicardial
layer appeared to be thin and compacted, but the apical endocardial layer of the left
ventricle was extremely thickened with prominent trabeculations in the endocardial layer and
deep intertrabecular recesses in a channel-like structure. Family history revealed that his
47-year-old brother also had LVNC but to a lesser degree. Their mother had two false tendons
in the left ventricular apex and both parents had severe CAD.
Left ventricular non-compaction is "incidentally" identified in a kindred with familial CAD.
The disease expressivity varies among affected individuals. Whether it is coincidental or there
is a genetic link is a question that awaits further investigation. (Cardiol J 2007; 14: 407-410
Case Reports
The 5th Indonesian Intensive and Acute Cardiovascular Care Meeting
Abstracts: Case Report
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