Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported

Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of cranio...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Archives of Pediatric Neurosurgery 2024-01, Vol.6 (1), p.e1942023
Hauptverfasser: Koko, Aliyu Muhammad, Lasseini, Ali, Jinjiri Isma, Nasiru, Bala Shehu, Bello
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 1
container_start_page e1942023
container_title Archives of Pediatric Neurosurgery
container_volume 6
creator Koko, Aliyu Muhammad
Lasseini, Ali
Jinjiri Isma, Nasiru
Bala Shehu, Bello
description Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus. Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome. Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus. Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.
doi_str_mv 10.46900/apn.v5i3.194
format Article
fullrecord <record><control><sourceid>gale_cross</sourceid><recordid>TN_cdi_crossref_primary_10_46900_apn_v5i3_194</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A782784509</galeid><sourcerecordid>A782784509</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2144-f5c0842d171bea95150f60bc0152d39acee6be2baf4f5adb496311a58a06fee83</originalsourceid><addsrcrecordid>eNpNkMFOwzAQRC0EElXpkbt_IMF2bCfhVkVAkYpACM7RxlmnRmkS2WlR_p5Ae0B72N3RzBweIbecxVLnjN3B0MVH5ZKY5_KCLIROVZRooS__3ddkFcIXY0xkSmciWRB8Aw_Bjc7QwkPn-gGaQ6DfbtzRAv3RGWjpy4Rtv8fOdU1vsEUKXU03U-3nb9hBewj39B2H3o-zg447pB48ttNZxPqGXFloA67Oe0k-Hx8-ik20fX16LtbbyAguZWSVYZkUNU95hZArrpjVrDKMK1EnORhEXaGowEqroK5krhPOQWXAtEXMkiWJT70NtFi6zvajBzNPjXtn-g6tm_V1mok0k4rlcyA6BYzvQ_Boy8G7Pfip5Kz841rOXMtfruXMNfkB6QNubA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported</title><source>EZB-FREE-00999 freely available EZB journals</source><creator>Koko, Aliyu Muhammad ; Lasseini, Ali ; Jinjiri Isma, Nasiru ; Bala Shehu, Bello</creator><creatorcontrib>Koko, Aliyu Muhammad ; Lasseini, Ali ; Jinjiri Isma, Nasiru ; Bala Shehu, Bello</creatorcontrib><description>Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus. Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome. Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus. Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.</description><identifier>ISSN: 2675-3626</identifier><identifier>EISSN: 2675-3626</identifier><identifier>DOI: 10.46900/apn.v5i3.194</identifier><language>eng</language><publisher>Sociedade Brasileira de Neurocirurgia Pediatrica</publisher><subject>Birth defects ; Conjoined twins ; Genetic disorders ; Hydrocephalus ; Myelomeningocele</subject><ispartof>Archives of Pediatric Neurosurgery, 2024-01, Vol.6 (1), p.e1942023</ispartof><rights>COPYRIGHT 2024 Sociedade Brasileira de Neurocirurgia Pediatrica</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-3742-5075 ; 0000-0002-7166-5734 ; 0009-0003-6601-6048 ; 0000-0001-9032-5172</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Koko, Aliyu Muhammad</creatorcontrib><creatorcontrib>Lasseini, Ali</creatorcontrib><creatorcontrib>Jinjiri Isma, Nasiru</creatorcontrib><creatorcontrib>Bala Shehu, Bello</creatorcontrib><title>Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported</title><title>Archives of Pediatric Neurosurgery</title><description>Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus. Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome. Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus. Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.</description><subject>Birth defects</subject><subject>Conjoined twins</subject><subject>Genetic disorders</subject><subject>Hydrocephalus</subject><subject>Myelomeningocele</subject><issn>2675-3626</issn><issn>2675-3626</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpNkMFOwzAQRC0EElXpkbt_IMF2bCfhVkVAkYpACM7RxlmnRmkS2WlR_p5Ae0B72N3RzBweIbecxVLnjN3B0MVH5ZKY5_KCLIROVZRooS__3ddkFcIXY0xkSmciWRB8Aw_Bjc7QwkPn-gGaQ6DfbtzRAv3RGWjpy4Rtv8fOdU1vsEUKXU03U-3nb9hBewj39B2H3o-zg447pB48ttNZxPqGXFloA67Oe0k-Hx8-ik20fX16LtbbyAguZWSVYZkUNU95hZArrpjVrDKMK1EnORhEXaGowEqroK5krhPOQWXAtEXMkiWJT70NtFi6zvajBzNPjXtn-g6tm_V1mok0k4rlcyA6BYzvQ_Boy8G7Pfip5Kz841rOXMtfruXMNfkB6QNubA</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Koko, Aliyu Muhammad</creator><creator>Lasseini, Ali</creator><creator>Jinjiri Isma, Nasiru</creator><creator>Bala Shehu, Bello</creator><general>Sociedade Brasileira de Neurocirurgia Pediatrica</general><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><orcidid>https://orcid.org/0000-0002-3742-5075</orcidid><orcidid>https://orcid.org/0000-0002-7166-5734</orcidid><orcidid>https://orcid.org/0009-0003-6601-6048</orcidid><orcidid>https://orcid.org/0000-0001-9032-5172</orcidid></search><sort><creationdate>20240101</creationdate><title>Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported</title><author>Koko, Aliyu Muhammad ; Lasseini, Ali ; Jinjiri Isma, Nasiru ; Bala Shehu, Bello</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2144-f5c0842d171bea95150f60bc0152d39acee6be2baf4f5adb496311a58a06fee83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Birth defects</topic><topic>Conjoined twins</topic><topic>Genetic disorders</topic><topic>Hydrocephalus</topic><topic>Myelomeningocele</topic><toplevel>online_resources</toplevel><creatorcontrib>Koko, Aliyu Muhammad</creatorcontrib><creatorcontrib>Lasseini, Ali</creatorcontrib><creatorcontrib>Jinjiri Isma, Nasiru</creatorcontrib><creatorcontrib>Bala Shehu, Bello</creatorcontrib><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><jtitle>Archives of Pediatric Neurosurgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koko, Aliyu Muhammad</au><au>Lasseini, Ali</au><au>Jinjiri Isma, Nasiru</au><au>Bala Shehu, Bello</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported</atitle><jtitle>Archives of Pediatric Neurosurgery</jtitle><date>2024-01-01</date><risdate>2024</risdate><volume>6</volume><issue>1</issue><spage>e1942023</spage><pages>e1942023-</pages><issn>2675-3626</issn><eissn>2675-3626</eissn><abstract>Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus. Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome. Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus. Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.</abstract><pub>Sociedade Brasileira de Neurocirurgia Pediatrica</pub><doi>10.46900/apn.v5i3.194</doi><orcidid>https://orcid.org/0000-0002-3742-5075</orcidid><orcidid>https://orcid.org/0000-0002-7166-5734</orcidid><orcidid>https://orcid.org/0009-0003-6601-6048</orcidid><orcidid>https://orcid.org/0000-0001-9032-5172</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2675-3626
ispartof Archives of Pediatric Neurosurgery, 2024-01, Vol.6 (1), p.e1942023
issn 2675-3626
2675-3626
language eng
recordid cdi_crossref_primary_10_46900_apn_v5i3_194
source EZB-FREE-00999 freely available EZB journals
subjects Birth defects
Conjoined twins
Genetic disorders
Hydrocephalus
Myelomeningocele
title Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T05%3A31%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Parasitic%20Craniopagus%20with%20Cervical%20Myelomeningocele%20and%20Hydrocephalus:%20Reporting%20the%20rarely%20Reported&rft.jtitle=Archives%20of%20Pediatric%20Neurosurgery&rft.au=Koko,%20Aliyu%20Muhammad&rft.date=2024-01-01&rft.volume=6&rft.issue=1&rft.spage=e1942023&rft.pages=e1942023-&rft.issn=2675-3626&rft.eissn=2675-3626&rft_id=info:doi/10.46900/apn.v5i3.194&rft_dat=%3Cgale_cross%3EA782784509%3C/gale_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_galeid=A782784509&rfr_iscdi=true