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Autor:
Pascal Christiaan Jan Visser, Maarten A Vink, Mark S Patterson, Aria Yazdanbakhsh, Fatih Arlan, Remko S Kuipers
Publikováno v:
BMJ case reports. 15(4)
A 31-year-old man with a history of hypertrophic cardiomyopathy and alcohol septal ablation one week before was presented after an out of hospital cardiac arrest in the setting of an anterior wall ST-elevation myocardial infarction. Immediate coronar
Publikováno v:
BMJ case reports. 15(2)
Mitral valve (MV) haemangiomas are rare primary cardiac tumours which may cause progressive cardiac failure as well as sudden death. We present a case of a 44-year-old woman referred for surgical correction of symptomatic severe mitral regurgitation.
Publikováno v:
BMJ case reports. 14(12)
A 30-year-old woman in her second pregnancy, which was complicated by gestational diabetes mellitus. She had an uneventful spontaneous vaginal delivery at 38 weeks+3 days of gestation. Day 1 postpartum, she developed sudden chest pain radiating to he
Publikováno v:
The neuroradiology journal. 35(6)
Background and Introduction Interrupted aortic arch (IAA) is a very rare congenital anomaly carrying high neonatal mortality rate if left untreated. Rarer still, is its presentation in teenage or adulthood. This condition has been found to be complic
Publikováno v:
BMJ case reports. 14(11)
A 34-year-old woman, a known case of valvular heart disease, post balloon pulmonary valvuloplasty done 8 years ago during her first pregnancy, presented with progressive exertional breathlessness with New York Heart Association class III symptoms in
Autor:
Yudai, Goto, Masataka, Nanto, Hideki, Oka, Nobukuni, Murakami, Toru, Nakagawa, Satoshi, Kimura, Yoshihiro, Iwamoto, Yasuo, Inoue, Keigo, Matsumoto, Junichi, Miyamoto, Naoya, Hashimoto
Publikováno v:
Journal of Neurosurgery. 137:1718-1726
OBJECTIVE Twig-like middle cerebral artery (T-MCA) is a rare congenital anomaly that is difficult to distinguish from moyamoya angiopathy (MMA), given the similarity of the angioarchitectures. The aim of this study was to gain insights into the radio
Autor:
Ibrahim Yildiz, Ibrahim Rencüzoğulları, Yavuz Karabağ, Muammer Karakayali, Inanc Artac, Mehmet Sait Gurevin
Publikováno v:
Revista da Associação Médica Brasileira, Volume: 68, Issue: 6, Pages: 802-807, Published: 24 JUN 2022
Revista da Associação Médica Brasileira v.68 n.6 2022
Revista da Associação Médica Brasileira
Associação Médica Brasileira (AMB)
instacron:AMB
Revista da Associação Médica Brasileira v.68 n.6 2022
Revista da Associação Médica Brasileira
Associação Médica Brasileira (AMB)
instacron:AMB
SUMMARY OBJECTIVE: A decrease in the left ventricular ejection fraction (≤40%) in the setting of ST-segment elevation myocardial infarction is a significant predictor of mortality in the young ST-segment elevation myocardial infarction population.
Publikováno v:
BMJ Case Rep
Congenital anomalies of the infrarenal inferior vena cava (IVC) are well described in adult life, however, little information exists on their associations in fetal life. Here, we describe a case of a monochorionic diamniotic (MCDA) twin pregnancy com
Autor:
Naoki Shirafuji, Yusuke Akitomi, Yoshinari Asaoka, Sae Murata, Haruko Tashiro, Atsushi Tanaka, Masayoshi Yamamoto, Hiroshi Kondo, Takatsugu Yamamoto, Kentaro Yamada, Ryo Miura
Publikováno v:
Internal Medicine. 61:1519-1524
A series of abdominal computed tomography scans of an asymptomatic 40-year-old woman with a history of umbilical cord blood transplantation (CBT) for leukemia at 19 years old revealed the long-term gradual development of a right hepatic vein thrombus
Autor:
Kevin C. Eddinger, Julia D. Glaser, Alison M. Pouch, Grace J. Wang, Benjamin M. Jackson, Paul J. Foley, Jordan B. Stoecker, Venkat Kalapatapu
Publikováno v:
Ann Vasc Surg
Background: The “crescent sign” is a hyperattenuating crescent-shaped region on CT within the mural thrombus or wall of an aortic aneurysm. Although it has previously been associated with aneurysm instability or impending rupture, the literature