Abstract

The term in was first coined by Johann Friedrich Meckel in the late 18th century to describe an encapsulated fetoid tumor within a fetus. Since then, fewer than 100 cases of fetus in fetu have been reported in the medical literature. The incidence of fetus in fetu is estimated to be approximately 1 per 500,000 births, 1 occurring relatively equally in male and female patients. 2 Debate exists as to whether fetus in fetu is a variant in the spectrum of monozygotic twinning or if it is simply a highly differentiated teratoma. The presence of a partial or whole vertebral column plus other appropriately situated axial or appendicular bones or organs constitutes the hallmark of fetus in fetu. 3 The conservative definition is the presence of a vertebral axis, which occurs in most cases. The more liberal definition was proposed by Gonzalez-Crussi, 4 who defined fetus in fetu as high organotypic development and presence of a vertebral axis with arrangement of tissues around this axis. It has been suggested that fetus in fetu is part of a spectrum of anomalous embryogenesis, including conjoined symmetric twins, parasitic fetuses, embryonic vestigial fetal inclusions, organized teratoma, and the twin reversed arterial perfusion sequence (also referred to as acardiac monster).

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call