Parasitic twin

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Parasitic twin
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Illustration of a man with a parasitic twin, alongside illustrations of two configurations of conjoined twins
Specialty Maternal–fetal medicine, neonatology   OOjs UI icon edit-ltr-progressive.svg

A parasitic twin, also known as an asymmetrical twin or unequal conjoined twin, occurs when a twin embryo begins developing in utero, but the pair does not fully separate, and one embryo maintains dominant development at the expense of the other. It results from the same processes that also produces vanishing twins and conjoined twins , and may represent a continuum between the two. In parasitic twins, one ceases development during gestation and is vestigial to a mostly fully formed, otherwise healthy individual twin. The undeveloped twin is termed as parasitic , because it is incompletely formed or wholly dependent on the body functions of the complete fetus. [1] The independent twin is called the autosite.

Contents

Variants

TRAP syndrome. The acardiac twin, left, cannot pump its own blood. The pump twin, right, supplies blood to the parasitic twin. Acardiac twin.jpg
TRAP syndrome. The acardiac twin, left, cannot pump its own blood. The pump twin, right, supplies blood to the parasitic twin.

TRAP sequence

The twin reversed arterial perfusion, or T.R.A.P. sequence, results in an 'acardiac twin', a parasitic twin that fails to develop a head, arms and a heart. The parasitic twin, little more than a torso with or without legs, receives its blood supply from the host twin by means of an umbilical cord-like structure, much like a fetus in fetu, except the acardiac twin is outside the autosite's body. The blood received by the parasitic twin has already been used by the normal fetus, and as such is already de-oxygenated, leaving little developmental nutrients for the acardiac twin. Because it is pumping blood for both itself and its acardiac twin, this causes extreme stress on the normal fetus' heart. Many T.R.A.P. pregnancies result in heart failure for the healthy twin. This twinning condition usually occurs very early in pregnancy. [2] A rare variant of the acardiac fetus is the acardius acormus where the head is well developed but the heart and the rest of the body are rudimentary. While it is thought that the classical T.R.A.P./Acardius sequence is due to a retrograde flow from the umbilical arteries of the pump twin to the iliac arteries of the acardiac twin resulting in preferential caudal perfusion, acardius acormus is thought to be a result of an early embryopathy. [3]

Others

Conjoined parasitic twins joined at the head are described as craniopagus or cephalopagus, and occipitalis if joined in the occipital region or parietalis if joined in the parietal region.

Craniopagus parasiticus is a general term for a parasitic head attached to the head of a more fully developed fetus or infant. [4]

Fetus in fetu sometimes is interpreted as a special case of parasitic twin, but may be a distinct entity.

Human

Animals

See also

Related Research Articles

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<span class="mw-page-title-main">Twin reversed arterial perfusion</span> Rare complication of monochorionic twin pregnancies

Twin reversed arterial perfusion sequence, also called TRAP sequence, TRAPS, or acardiac twinning, is a rare complication of monochorionic twin pregnancies. It is a severe variant of twin-to-twin transfusion syndrome (TTTS). In addition to the twins' blood systems being connected instead of independent, one twin, called the acardiac twin, TRAP fetus or acardius, is severely malformed. The heart is missing or deformed, hence the name "acardiac", as are the upper structures of the body. The legs may be partially present or missing, and internal structures of the torso are often poorly formed. The other twin is usually normal in appearance. The normal twin, called the pump twin, drives blood through both fetuses. It is called "reversed arterial perfusion" because in the acardiac twin the blood flows in a reversed direction.

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References

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  1. "Parasitic Twins | The Embryo Project Encyclopedia". embryo.asu.edu. Retrieved 2022-02-18.
  2. "Acardiac Twin or TRAP Sequence". University of California, San Francisco. 2007-04-26. Archived from the original on 2012-07-08. Retrieved 2007-05-30.
  3. Abi Nader Khalil, Whitten Sara Melissa, Filippi Elisa, Scott Rose-Mary, Jauniaux Eric. Dichorionic triamniotic triplet pregnancy complicated by acardius acormus. Fetal Diagnosis and Therapy 2009;26(1):45-9.
  4. Aquino DB, Timmons C, Burns D, Lowichik A (1997). "Craniopagus parasiticus: a case illustrating its relationship to craniopagus conjoined twinning". Pediatric Pathology and Laboratory Medicine. 17 (6): 939–44. doi:10.1080/107710497174381. PMID   9353833.

Further reading