Congenitally corrected transposition.

Congenitally corrected transposition is a rare cardiac malformation characterized by the combination of discordant atrioventricular and ventriculo-arterial connections, usually accompanied by other cardiovascular malformations. Incidence has been reported to be around 1/33,000 live births, accounting for approximately 0.05% of congenital heart malformations.

Is there still a role for cardiac autopsy in 2007?

Concerns have emerged in recent years with regard to the role to be played by the pathologist in reaching a final diagnosis. When considering the field of the congenitally malformed heart, it is true that the richness of detail now provided by imaging techniques is truly amazing. Alongside these developments, there has also been a significant decline in the number of autopsies performed in tertiary medial centres around the World.

Conjoined twins: morphogenesis of the heart and a review.

Five cases of conjoined twins have been studied. These included three thoracopagus twins, one monocephalus diprosopus (prosop = face), and one dicephalus dipus dibrachus. The thoracopagus twins were conjoined only from the upper thorax to the umbilicus with a normal foregut.

Fetus-in-fetu form of monozygotic twinning with retroperitoneal teratoma.

One of the commonest defects of blastogenesis is monozygotic twinning resulting in separate or conjoint twins, the latter including a category of internal, "endoparasitic," or fetus-in-fetu twins. We report the third known instance of endoparasitic twinning associated with a benign teratoma at age 1. The host, twin, and teratoma were monozygotic by DNA analysis.

Apparent encephalocele in twin fetus papyraceus with twin-reversal arterial perfusion.

An apparently iniencephalic or exencephalic monoamniotic monochorionic female twin fetus, delivered as a fetus papyraceus at 28 weeks of gestation, had severe anomalies of the central nervous system and spine, including occipital encephalocele with a defect of the occipital bone. The encephalocele contained a spherical mass of autolyzed brain tissue without identifiable cerebellum or vermis. The cervical canal was widely patent dorsally, there were severe bony anomalies, including agenesis and fusion of vertebrae in the cervicothoracic spine.