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      Pre- and postnatal findings of a dicephalus tetrabrachius-dipus conjoined twins with a diaphragmatic hernia Translated title: Achados pré e pós-natais de um gêmeo fusionado dicephalus tetrabrachius-dipus apresentando uma hérnia diafragmática

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          Abstract

          Dear. Editor, A 17-year-old primigravida attended the service at the 31st gestational week for evaluation of monochorionic, monoamniotic twin gestation. First trimester sonographic images were not available. Morphological ultrasonography (US) demonstrated the fetuses joined at the level of their abdomen and pelvis, and presence of a diaphragmatic hernia in the second twin. The woman denied previous history of health problems or use of medicines and illicit drugs. Her 25-year-old husband was healthy, with negative history of consanguinity. No family history of genetic diseases and malformations was reported. Fetal magnetic resonance imaging (MRI) revealed a dicephalus tetrabrachius-dipus conjoined twin. The fetus at right presented with a left diaphragmatic hernia containing stomach, small bowel and colon. The twins shared a single liver and a urinary bladder. Two kidneys connected each other at the level of their lower poles, and two vertebral spines were fused at the level of the sacrum (Figure 1). Echocardiography was normal. Figure 1 Fetal MRI T2-weighted image showing the dicephalus tetrabrachiusdipus conjoined twin. The fetus at right presents with a left diaphragmatic hernia. Mediastinal structures (heart and large vessels) and pulmonary hypoplasia (A) are identified. Hepatic fusion is also visualized (B). The conjoined twin was born by Cesarean section at the 35th gestational week, weighting 3,765 grams. Upper eyelid coloboma was found in the twin with diaphragmatic hernia. Radiographic evaluation demonstrated vertebral spines fusion at the level of the lumbar region, besides the presence of bowel loops in the thoracic cavity of the twin at right (Figure 2). Surgery for the diaphragmatic hernia could not be performed. The conjoined twin died at the 17th day of life. Figure 2 Postnatal image of the dicephalus tetrabrachius-dipus twin (A). Radiographic evaluation showing vertebral spines fusion at the L4 level and a single pelvis. A diaphragmatic hernia is observed in the fetus at right (there is evidence of the presence of bowel loops within the thoracic cavity), without identification of the heart and airways (B). Imperfect twinning occurs in approximately one per 250,000 live births(1,2) and is classified according to the fusion site added by the term pagus (3). "Parapagus" twins (meaning "extensive lateral fusion") correspond to 28% of cases of conjoined twins(4). The subtype dicephalus tetrabrachius-dipus, as observed in the present case, is considered rare (4/10,000,000 births)(5). US has shown to be the best method for initial evaluation of the gestation, and can identify imperfect twinning as early as at the 12th gestational week(1). However, US is subjected to limitations such as maternal biotype and presence of either oligohydramnios or anhydramnios. On the other hand, MRI represents a good complementary tool since it does not present such limitations, while providing images with better resolution(6). Additionally, it serves as support for a possible surgical planning, since it allows for visualization and detection of abnormalities which otherwise would be missed or inconclusive at US(2). In the present case, MRI was relevant, particularly in the determination of the type of imperfect twinning as well as of the extent of fusion and sharing of organs. Congenital abnormalities not related to the fusion site are observed in 10% to 20% of cases of conjoined twins. Diaphragmatic hernia such as the one observed in the present case is one of the described findings(7). Upper eyelid coloboma that was also identified in the present case is considered to be a rare abnormality(8). Thus, the correct determination of the type of imperfect twinning as well as of the fusion extent may be useful in the evaluation of the condition severity and in the postnatal surgical planning. Determining the severity of the condition is of paramount importance considering that the Brazilian laws allows for gestation termination in cases where the extrauterine life is not possible(3).

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          Theoretical and analytical embryology of conjoined twins: part I: embryogenesis.

          R. Spencer (2000)
          A review of over 1,800 publications concerning the embryology and pathologic anatomy of conjoined twins provides convincing evidence that they all result from the secondary union of two originally separate monovular embryonic discs. This "fusion" theory seems to be confirmed by the adjustments to union and the pattern and incidence of specific anomalies at the proposed sites of conjunction in more than 1,200 cases, all of which can be arranged in two uninterrupted series of cases, the one united dorsally (in the neural tube) and the other, ventrally (over a shared a yolk sac). No theoretical "fission" of the vertebrate embryo at any stage of development, in any plane, in any direction can explain (1) the selection of the observed sites of fusion, (2) the details of the union, or (3) the limitation to the specific areas in which the twins are found to be joined. Part I of this disquisition deals with the pertinent normal and theoretical embryology, the adjustments to union, and the parasitic cases, as well as conjoined triplets and quadruplets, and a comparison of oviparous and viviparous embryos. Part II (in a subsequent issue of this journal) will compare and correlate the abnormalities of the various organ systems involved in 1,200 cases. Copyright 2000 Wiley-Liss, Inc.
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            The natural history of prenatally diagnosed conjoined twins.

            Accurate prenatal diagnosis of complex anatomic connections and associated anomalies has only been possible recently with the use of ultrasonography, echocardiography, and fetal magnetic resonance imaging (MRI). To assess the impact of improved antenatal diagnosis in the management and outcome of conjoined twins, the authors reviewed their experience with 14 cases. A retrospective review of prenatally diagnosed conjoined twins referred to our institution from 1996 to present was conducted. In 14 sets of conjoined twins, there were 10 thoracoomphalopagus, 2 dicephalus tribrachius dipus, 1 ischiopagus, and 1 ischioomphalopagus. The earliest age at diagnosis was 9 weeks' gestation (range, 9 to 29; mean, 20). Prenatal imaging with ultrasonography, echocardiography, and ultrafast fetal MRI accurately defined the shared anatomy in all cases. Associated anomalies included cardiac malformations (11 of 14), congenital diaphragmatic hernia (4 of 14), abdominal wall defects (2 of 14), and imperforate anus (2 of 14). Three sets of twins underwent therapeutic abortion, 1 set of twins died in utero, and 10 were delivered via cesarean section at a mean gestational age of 34 weeks. There were 5 individual survivors in the series after separation (18%). In one case, in which a twin with a normal heart perfused the cotwin with a rudimentary heart, the ex utero intrapartum treatment procedure (EXIT) was utilized because of concern that the normal twin would suffer immediate cardiac decompensation at birth. This EXIT-to-separation strategy allowed prompt control of the airway and circulation before clamping the umbilical cord and optimized control over a potentially emergent situation, leading to survival of the normal cotwin. In 2 sets of twins in which each twin had a normal heart, tissue expanders were inserted before separation. Advances in prenatal diagnosis allow detailed, accurate evaluations of conjoined twins. Careful prenatal studies may uncover cases in which emergent separation at birth is lifesaving. Copyright 2002 by W.B. Saunders Company.
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              Imaging of conjoined twins.

              The incidence of conjoined twins is estimated to be around 1 in 250,000 live births. There is a distinct female predominance. In this paper the imaging of conjoined twins both antenatally and postnatally is reviewed, in particular taking into consideration recent advances with multidetector CT. Accurate counselling of parents regarding the likely outcome of the pregnancy and the likelihood of successful separation is dependent on good prenatal imaging with ultrasound and MRI. Planning of postnatal surgical separation is aided by accurate preoperative imaging which, depending on the conjoined area, will encompass many imaging modalities, but often relies heavily on CT scanning.
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                Author and article information

                Journal
                Radiol Bras
                Radiol Bras
                rb
                Radiologia Brasileira
                Colégio Brasileiro de Radiologia e Diagnóstico por Imagem
                0100-3984
                1678-7099
                Jan-Feb 2015
                Jan-Feb 2015
                : 48
                : 1
                : 61-62
                Affiliations
                [1 ]Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brasil
                [2 ]Hospital Materno Infantil Presidente Vargas (HMIPV), Porto Alegre, RS, Brasil
                Author notes
                Mailing Address: Dr. Rafael Fabiano Machado Rosa, Rua Sarmento Leite, 245/403, Centro, Porto Alegre, RS, Brazil, 90050-170. E-mail: rfmr@ 123456terra.com.br
                Article
                10.1590/0100-3984.2013.0021
                4366033
                25798012
                02dbb741-720f-4f32-a58a-44678e973149
                © Colégio Brasileiro de Radiologia e Diagnóstico por Imagem

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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