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A Rare Form of Heteropagus Twinning: Three-Armed Infant with Spinal Dysraphism

An ectopic or accessory limb attached to the back is an extremely rare and strange condition, and there are only a few documented cases in the worldwide literature. The first case was described by Jones and Larkin (1889). There are several theories regarding the origin of this condition. Asymmetric...

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Autores principales: Solak, Aynur, Ergün, Sonnaz, Polat, İpek, Şahin, Neslın, Genç, Berhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530761/
https://www.ncbi.nlm.nih.gov/pubmed/23304600
http://dx.doi.org/10.1155/2012/831649
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author Solak, Aynur
Ergün, Sonnaz
Polat, İpek
Şahin, Neslın
Genç, Berhan
author_facet Solak, Aynur
Ergün, Sonnaz
Polat, İpek
Şahin, Neslın
Genç, Berhan
author_sort Solak, Aynur
collection PubMed
description An ectopic or accessory limb attached to the back is an extremely rare and strange condition, and there are only a few documented cases in the worldwide literature. The first case was described by Jones and Larkin (1889). There are several theories regarding the origin of this condition. Asymmetric conjoined twinning which is located dorsally in the vertebral column (rachipagus) is the most probable diagnosis of our patient. Conjoined twinning is very rare and the incidence is 1 per 50 000 live births. Rachipagus is even rarer, with no more than 30 case reports so far (Chadha et al. (1993, 2006)). In this report, we present a patient who underwent successful surgical excision of a third arm attached to the back in the midline over the low-dorsal region. Differential diagnoses including teratoma and fetus in fetu are discussed.
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spelling pubmed-35307612013-01-09 A Rare Form of Heteropagus Twinning: Three-Armed Infant with Spinal Dysraphism Solak, Aynur Ergün, Sonnaz Polat, İpek Şahin, Neslın Genç, Berhan Case Rep Pediatr Case Report An ectopic or accessory limb attached to the back is an extremely rare and strange condition, and there are only a few documented cases in the worldwide literature. The first case was described by Jones and Larkin (1889). There are several theories regarding the origin of this condition. Asymmetric conjoined twinning which is located dorsally in the vertebral column (rachipagus) is the most probable diagnosis of our patient. Conjoined twinning is very rare and the incidence is 1 per 50 000 live births. Rachipagus is even rarer, with no more than 30 case reports so far (Chadha et al. (1993, 2006)). In this report, we present a patient who underwent successful surgical excision of a third arm attached to the back in the midline over the low-dorsal region. Differential diagnoses including teratoma and fetus in fetu are discussed. Hindawi Publishing Corporation 2012 2012-12-12 /pmc/articles/PMC3530761/ /pubmed/23304600 http://dx.doi.org/10.1155/2012/831649 Text en Copyright © 2012 Aynur Solak et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Solak, Aynur
Ergün, Sonnaz
Polat, İpek
Şahin, Neslın
Genç, Berhan
A Rare Form of Heteropagus Twinning: Three-Armed Infant with Spinal Dysraphism
title A Rare Form of Heteropagus Twinning: Three-Armed Infant with Spinal Dysraphism
title_full A Rare Form of Heteropagus Twinning: Three-Armed Infant with Spinal Dysraphism
title_fullStr A Rare Form of Heteropagus Twinning: Three-Armed Infant with Spinal Dysraphism
title_full_unstemmed A Rare Form of Heteropagus Twinning: Three-Armed Infant with Spinal Dysraphism
title_short A Rare Form of Heteropagus Twinning: Three-Armed Infant with Spinal Dysraphism
title_sort rare form of heteropagus twinning: three-armed infant with spinal dysraphism
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530761/
https://www.ncbi.nlm.nih.gov/pubmed/23304600
http://dx.doi.org/10.1155/2012/831649
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