We report the case of a patient with dextrocardia and situs inversus totalis associated with obstructive coronariopathy in the anterior and posterior descending arteries, right coronary artery, first diagonal branch and left marginal branch. The patient underwent coronary artery bypass grafting surgery. This surgery has been rarely reported in literature and we found only one similar case in th...

Biliary atresia (BA) is a rare disease and the end result of a destructive, inflammatory cholangiopathy, leading to fibrosis and biliary cirrhosis. It is classified into syndromic variety with various congenital anomalies and non-syndromic (isolated anomaly). We present here a 1-month-old female child with the syndromic variety of BA associated with polysplenia syndrome, dextrocardia, situs inv...

NOMALOUS inferior vena cava with azygos or hemiazygos continuation has been considered to be a very rare anomaly in the past. However, since the development of cardiac catheterization and angiocardiography, this congenital abnormality has been reported with increasing frequency. This anomaly is usually associated with other cardiovascular defect, and there are few reported cases without other m...

An 82-year-old female with a history of situs inversus totalis visited our hospital with complaints of abdominal pain and fever for 2 days. She had history of diabetes mellitus, cerebral infarction, and Alzheimer’s disease, and underwent Billroth-ll (B-II) gastrectomy due to stomach cancer 15 years previously. General appearance was acute ill looking and there was tenderness on right upper quad...

Situs inversus totalis (SIT) is a rare congenital anomaly characterized by complete transposition of abdominal and thoracic organs. Change in anatomical disposition of the organs not only influences the location of symptoms and signs arising from a diseased organ, but also imposes special demands on the diagnostic and surgical skills of the surgeon. We discuss two cases of SIT, outline how the ...

A 6-year-old girl is described who has congenital megaloblastic anemia which completely responded only to pharmacologic doses of thiamine. Relapse was observed twice when the drug was discontinued. The reintroduction of thiamine caused a prompt reticulocytosis and a rise in hemoglobin concentration. Other abnormalities included latent diabetes mellitus, sensorineural deafness, and "situs invers...