scholarly journals Cardiopatia complexa congênita associada a situs inversus totalis em recém nascido: relato de caso/ Complex congenital heart disease associated with situs inversus totalis in a newborn: a case report

2021 ◽  
Vol 4 (6) ◽  
pp. 23785-23794
Author(s):  
Arielly Carvalho Rosa ◽  
Andressa Sousa Aguiar ◽  
Alinne Katienny Lima Silva Macambira ◽  
Gabriel Varão da Silva
2016 ◽  
Vol 9 (2) ◽  
pp. 254-256
Author(s):  
Andrew C. Chatzis ◽  
Alexandros J. Tsoutsinos ◽  
Meletios A. Kanakis ◽  
Constantinos A. Contrafouris ◽  
Spyros Rammos ◽  
...  

2017 ◽  
Vol 9 (3) ◽  
pp. 364-367
Author(s):  
Abid Iqbal ◽  
Sabarinath Menon ◽  
Baiju S. Dharan ◽  
Kapilamoorthy Tirur Raman ◽  
Jayakumar Karunakaran

Submitral aneurysms are rare clinical entities occurring predominantly in young adults of African descent. A host of etiologies have been proposed for this entity. We present a unique case of submitral aneurysm which developed after pulmonary artery banding in a three-year-old girl with complex congenital heart disease. The aneurysmal sac was burrowing into the interatrial septum.


2016 ◽  
Vol 31 (1) ◽  
pp. 41-45
Author(s):  
Khandker Md Nurus Sabah ◽  
Abdul Wadud Chowdhury ◽  
Mohammad Shahidul Islam ◽  
Mohsin Ahmed ◽  
Gaffar Amin ◽  
...  

Introduction: Brain abscess is a complication of congenital cyanotic heart disease with or without shunt anomaly. It is more common in children. Here, we delineated a case of 19-year-old young Bangladeshi - Bengali male who presenting with brain abscess, an unusual presentation of cyanotic complex congenital heart disease. This case report focuses not only on the unusual presentation of congenital heart disease but also emphasizes the importance of early recognition of neurological complication for referal management.Bangladesh Heart Journal 2016; 31(1) : 41-45


2020 ◽  
Vol 2020 ◽  
pp. 1-5
Author(s):  
Ioannis A. Ziogas ◽  
Alexandros P. Evangeliou ◽  
Olga Tsachouridou ◽  
Alexandra Arvanitaki ◽  
Afroditi Tsona ◽  
...  

Introduction. Blood culture-negative infective endocarditis (BCNIE) can present subtly and is associated with a diagnostic delay leading to increased morbidity and mortality. Case Report. We present the case of an 18-year-old male with a history of complex congenital heart disease and 3-year intermittent episodes of fever of unknown origin, who was referred to our hospital for upper and lower extremity focal seizures. Laboratory blood tests were normal, blood cultures were negative, and brain imaging revealed an abscess. Cardiology consultation was requested, and transthoracic echocardiography revealed an intracardiac vegetation. Empiric antibiotic treatment with sultamicillin, gentamycin, and meropenem was initiated. Serology testing was positive for Coxiella burnetii, and the diagnosis of BCNIE was established. The antibiotic course was changed to oral doxycycline for 36 months and led to resolution of IE, with no vegetation detected on TTE after 15 months. Conclusion. BCNIE is a life-threatening disease entity that can lead to severe complications, such as valve regurgitation, emboli, and death. Patients with congenital heart disease are particularly vulnerable to IE. Timely diagnosis and antibiotic management are of paramount importance in order to avoid the potentially fatal sequelae.


2013 ◽  
Vol 8 (2) ◽  
pp. 128-133
Author(s):  
Md Faruque ◽  
Md Abdur Rashid ◽  
MA Muttalib ◽  
Syed Aminul Islam ◽  
Md Hafizur Rahman

Congenital Heart disease is although uncommon but is not rare. Complex congenital Heart disease is more rare. The survivality is less. Most of the patient die in the Early childhood. Our patient survive up to the age of 23 yrs. Early diagnosis & early corrective surgery will prolong the survivality & even normal life. DOI: http://dx.doi.org/10.3329/uhj.v8i2.16086 University Heart Journal Vol. 8, No. 2, July 2012


2019 ◽  
Vol 26 (4) ◽  
pp. 4-6
Author(s):  
AHJ Ong ◽  
SMY Toh ◽  
TJ Muhammad ◽  
MN Norazrulrizal ◽  
KK Sia

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