Mature ruptured sacrococcygeal teratoma in a 1-day old neonate

Sacrococcygeal teratomas (SCTs) are rare congenital tumors that are derived from embryonic germ cell layers [1]. They are the most common extragonadal germ cell tumors (GCTs) in the neonate, with a reported incidence of 1 in 35 000 births [2]. Teratomas are made of tissues that derive from three ger...
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Autor*in:	Boumediene ABOU-BEKR [verfasserIn] Salah Eddine Oussama KACIMI [verfasserIn] Omar RIFFI [verfasserIn] Chahrazed BOGHARI [verfasserIn] Selma Nihel KLOUCHE DJEDID [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2022

Schlagwörter:	Sacrococcygeal teratoma Rupture Surgery

Übergeordnetes Werk:	In: Journal of Pediatric Surgery Case Reports - Elsevier, 2015, 81(2022), Seite 102245-
Übergeordnetes Werk:	volume:81 ; year:2022 ; pages:102245-

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.1016/j.epsc.2022.102245

Katalog-ID:	DOAJ044784325

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520			\|a Sacrococcygeal teratomas (SCTs) are rare congenital tumors that are derived from embryonic germ cell layers [1]. They are the most common extragonadal germ cell tumors (GCTs) in the neonate, with a reported incidence of 1 in 35 000 births [2]. Teratomas are made of tissues that derive from three germinal layers (ectoderm, endoderm, and mesoderm). Sacrococcygeal teratomas are more common in girls, with a sex ratio of 1:4 [3]. The most frequent location of teratoma in children is the sacrococcygeal area [4]. Many sacrococcygeal teratoma cases are diagnosed prenatally with routine ultrasonography between the 22nd and the 34th week of gestation. However, access to routine prenatal ultrasound in low and middle income countries is limited [5]. Antenatal diagnosis is essential to the pregnancy management and to prevent neonatal death by identifying fetuses that are at a higher risk of complications and planning an adequate intervention when needed [6]. This case is reported to describe a North African neonate presenting with a sacrococcygeal teratoma at birth without prior antenatal diagnosis, and highlight the need for prenatal routine care in low and middle income countries.
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spelling	10.1016/j.epsc.2022.102245 doi (DE-627)DOAJ044784325 (DE-599)DOAJ59b8d8e486884c8fbc6fdc71354c132d DE-627 ger DE-627 rakwb eng RJ1-570 RD1-811 Boumediene ABOU-BEKR verfasserin aut Mature ruptured sacrococcygeal teratoma in a 1-day old neonate 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Sacrococcygeal teratomas (SCTs) are rare congenital tumors that are derived from embryonic germ cell layers [1]. They are the most common extragonadal germ cell tumors (GCTs) in the neonate, with a reported incidence of 1 in 35 000 births [2]. Teratomas are made of tissues that derive from three germinal layers (ectoderm, endoderm, and mesoderm). Sacrococcygeal teratomas are more common in girls, with a sex ratio of 1:4 [3]. The most frequent location of teratoma in children is the sacrococcygeal area [4]. Many sacrococcygeal teratoma cases are diagnosed prenatally with routine ultrasonography between the 22nd and the 34th week of gestation. However, access to routine prenatal ultrasound in low and middle income countries is limited [5]. Antenatal diagnosis is essential to the pregnancy management and to prevent neonatal death by identifying fetuses that are at a higher risk of complications and planning an adequate intervention when needed [6]. This case is reported to describe a North African neonate presenting with a sacrococcygeal teratoma at birth without prior antenatal diagnosis, and highlight the need for prenatal routine care in low and middle income countries. Sacrococcygeal teratoma Rupture Surgery Pediatrics Salah Eddine Oussama KACIMI verfasserin aut Omar RIFFI verfasserin aut Chahrazed BOGHARI verfasserin aut Selma Nihel KLOUCHE DJEDID verfasserin aut In Journal of Pediatric Surgery Case Reports Elsevier, 2015 81(2022), Seite 102245- (DE-627)74606571X (DE-600)2715451-8 22135766 nnns volume:81 year:2022 pages:102245- https://doi.org/10.1016/j.epsc.2022.102245 kostenfrei https://doaj.org/article/59b8d8e486884c8fbc6fdc71354c132d kostenfrei http://www.sciencedirect.com/science/article/pii/S2213576622000720 kostenfrei https://doaj.org/toc/2213-5766 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 81 2022 102245-
allfields_unstemmed	10.1016/j.epsc.2022.102245 doi (DE-627)DOAJ044784325 (DE-599)DOAJ59b8d8e486884c8fbc6fdc71354c132d DE-627 ger DE-627 rakwb eng RJ1-570 RD1-811 Boumediene ABOU-BEKR verfasserin aut Mature ruptured sacrococcygeal teratoma in a 1-day old neonate 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Sacrococcygeal teratomas (SCTs) are rare congenital tumors that are derived from embryonic germ cell layers [1]. They are the most common extragonadal germ cell tumors (GCTs) in the neonate, with a reported incidence of 1 in 35 000 births [2]. Teratomas are made of tissues that derive from three germinal layers (ectoderm, endoderm, and mesoderm). Sacrococcygeal teratomas are more common in girls, with a sex ratio of 1:4 [3]. The most frequent location of teratoma in children is the sacrococcygeal area [4]. Many sacrococcygeal teratoma cases are diagnosed prenatally with routine ultrasonography between the 22nd and the 34th week of gestation. However, access to routine prenatal ultrasound in low and middle income countries is limited [5]. Antenatal diagnosis is essential to the pregnancy management and to prevent neonatal death by identifying fetuses that are at a higher risk of complications and planning an adequate intervention when needed [6]. This case is reported to describe a North African neonate presenting with a sacrococcygeal teratoma at birth without prior antenatal diagnosis, and highlight the need for prenatal routine care in low and middle income countries. Sacrococcygeal teratoma Rupture Surgery Pediatrics Salah Eddine Oussama KACIMI verfasserin aut Omar RIFFI verfasserin aut Chahrazed BOGHARI verfasserin aut Selma Nihel KLOUCHE DJEDID verfasserin aut In Journal of Pediatric Surgery Case Reports Elsevier, 2015 81(2022), Seite 102245- (DE-627)74606571X (DE-600)2715451-8 22135766 nnns volume:81 year:2022 pages:102245- https://doi.org/10.1016/j.epsc.2022.102245 kostenfrei https://doaj.org/article/59b8d8e486884c8fbc6fdc71354c132d kostenfrei http://www.sciencedirect.com/science/article/pii/S2213576622000720 kostenfrei https://doaj.org/toc/2213-5766 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 81 2022 102245-
allfieldsGer	10.1016/j.epsc.2022.102245 doi (DE-627)DOAJ044784325 (DE-599)DOAJ59b8d8e486884c8fbc6fdc71354c132d DE-627 ger DE-627 rakwb eng RJ1-570 RD1-811 Boumediene ABOU-BEKR verfasserin aut Mature ruptured sacrococcygeal teratoma in a 1-day old neonate 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Sacrococcygeal teratomas (SCTs) are rare congenital tumors that are derived from embryonic germ cell layers [1]. They are the most common extragonadal germ cell tumors (GCTs) in the neonate, with a reported incidence of 1 in 35 000 births [2]. Teratomas are made of tissues that derive from three germinal layers (ectoderm, endoderm, and mesoderm). Sacrococcygeal teratomas are more common in girls, with a sex ratio of 1:4 [3]. The most frequent location of teratoma in children is the sacrococcygeal area [4]. Many sacrococcygeal teratoma cases are diagnosed prenatally with routine ultrasonography between the 22nd and the 34th week of gestation. However, access to routine prenatal ultrasound in low and middle income countries is limited [5]. Antenatal diagnosis is essential to the pregnancy management and to prevent neonatal death by identifying fetuses that are at a higher risk of complications and planning an adequate intervention when needed [6]. This case is reported to describe a North African neonate presenting with a sacrococcygeal teratoma at birth without prior antenatal diagnosis, and highlight the need for prenatal routine care in low and middle income countries. Sacrococcygeal teratoma Rupture Surgery Pediatrics Salah Eddine Oussama KACIMI verfasserin aut Omar RIFFI verfasserin aut Chahrazed BOGHARI verfasserin aut Selma Nihel KLOUCHE DJEDID verfasserin aut In Journal of Pediatric Surgery Case Reports Elsevier, 2015 81(2022), Seite 102245- (DE-627)74606571X (DE-600)2715451-8 22135766 nnns volume:81 year:2022 pages:102245- https://doi.org/10.1016/j.epsc.2022.102245 kostenfrei https://doaj.org/article/59b8d8e486884c8fbc6fdc71354c132d kostenfrei http://www.sciencedirect.com/science/article/pii/S2213576622000720 kostenfrei https://doaj.org/toc/2213-5766 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 81 2022 102245-
allfieldsSound	10.1016/j.epsc.2022.102245 doi (DE-627)DOAJ044784325 (DE-599)DOAJ59b8d8e486884c8fbc6fdc71354c132d DE-627 ger DE-627 rakwb eng RJ1-570 RD1-811 Boumediene ABOU-BEKR verfasserin aut Mature ruptured sacrococcygeal teratoma in a 1-day old neonate 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Sacrococcygeal teratomas (SCTs) are rare congenital tumors that are derived from embryonic germ cell layers [1]. They are the most common extragonadal germ cell tumors (GCTs) in the neonate, with a reported incidence of 1 in 35 000 births [2]. Teratomas are made of tissues that derive from three germinal layers (ectoderm, endoderm, and mesoderm). Sacrococcygeal teratomas are more common in girls, with a sex ratio of 1:4 [3]. The most frequent location of teratoma in children is the sacrococcygeal area [4]. Many sacrococcygeal teratoma cases are diagnosed prenatally with routine ultrasonography between the 22nd and the 34th week of gestation. However, access to routine prenatal ultrasound in low and middle income countries is limited [5]. Antenatal diagnosis is essential to the pregnancy management and to prevent neonatal death by identifying fetuses that are at a higher risk of complications and planning an adequate intervention when needed [6]. This case is reported to describe a North African neonate presenting with a sacrococcygeal teratoma at birth without prior antenatal diagnosis, and highlight the need for prenatal routine care in low and middle income countries. Sacrococcygeal teratoma Rupture Surgery Pediatrics Salah Eddine Oussama KACIMI verfasserin aut Omar RIFFI verfasserin aut Chahrazed BOGHARI verfasserin aut Selma Nihel KLOUCHE DJEDID verfasserin aut In Journal of Pediatric Surgery Case Reports Elsevier, 2015 81(2022), Seite 102245- (DE-627)74606571X (DE-600)2715451-8 22135766 nnns volume:81 year:2022 pages:102245- https://doi.org/10.1016/j.epsc.2022.102245 kostenfrei https://doaj.org/article/59b8d8e486884c8fbc6fdc71354c132d kostenfrei http://www.sciencedirect.com/science/article/pii/S2213576622000720 kostenfrei https://doaj.org/toc/2213-5766 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 81 2022 102245-
language	English
source	In Journal of Pediatric Surgery Case Reports 81(2022), Seite 102245- volume:81 year:2022 pages:102245-
sourceStr	In Journal of Pediatric Surgery Case Reports 81(2022), Seite 102245- volume:81 year:2022 pages:102245-
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Sacrococcygeal teratoma Rupture Surgery Pediatrics
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container_title	Journal of Pediatric Surgery Case Reports
authorswithroles_txt_mv	Boumediene ABOU-BEKR @@aut@@ Salah Eddine Oussama KACIMI @@aut@@ Omar RIFFI @@aut@@ Chahrazed BOGHARI @@aut@@ Selma Nihel KLOUCHE DJEDID @@aut@@
publishDateDaySort_date	2022-01-01T00:00:00Z
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language_de	englisch
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callnumber-first	R - Medicine
author	Boumediene ABOU-BEKR
spellingShingle	Boumediene ABOU-BEKR misc RJ1-570 misc RD1-811 misc Sacrococcygeal teratoma misc Rupture misc Surgery misc Pediatrics Mature ruptured sacrococcygeal teratoma in a 1-day old neonate
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topic_title	RJ1-570 RD1-811 Mature ruptured sacrococcygeal teratoma in a 1-day old neonate Sacrococcygeal teratoma Rupture Surgery
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title	Mature ruptured sacrococcygeal teratoma in a 1-day old neonate
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title_full	Mature ruptured sacrococcygeal teratoma in a 1-day old neonate
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author_browse	Boumediene ABOU-BEKR Salah Eddine Oussama KACIMI Omar RIFFI Chahrazed BOGHARI Selma Nihel KLOUCHE DJEDID
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title_sort	mature ruptured sacrococcygeal teratoma in a 1-day old neonate
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title_auth	Mature ruptured sacrococcygeal teratoma in a 1-day old neonate
abstract	Sacrococcygeal teratomas (SCTs) are rare congenital tumors that are derived from embryonic germ cell layers [1]. They are the most common extragonadal germ cell tumors (GCTs) in the neonate, with a reported incidence of 1 in 35 000 births [2]. Teratomas are made of tissues that derive from three germinal layers (ectoderm, endoderm, and mesoderm). Sacrococcygeal teratomas are more common in girls, with a sex ratio of 1:4 [3]. The most frequent location of teratoma in children is the sacrococcygeal area [4]. Many sacrococcygeal teratoma cases are diagnosed prenatally with routine ultrasonography between the 22nd and the 34th week of gestation. However, access to routine prenatal ultrasound in low and middle income countries is limited [5]. Antenatal diagnosis is essential to the pregnancy management and to prevent neonatal death by identifying fetuses that are at a higher risk of complications and planning an adequate intervention when needed [6]. This case is reported to describe a North African neonate presenting with a sacrococcygeal teratoma at birth without prior antenatal diagnosis, and highlight the need for prenatal routine care in low and middle income countries.
abstractGer	Sacrococcygeal teratomas (SCTs) are rare congenital tumors that are derived from embryonic germ cell layers [1]. They are the most common extragonadal germ cell tumors (GCTs) in the neonate, with a reported incidence of 1 in 35 000 births [2]. Teratomas are made of tissues that derive from three germinal layers (ectoderm, endoderm, and mesoderm). Sacrococcygeal teratomas are more common in girls, with a sex ratio of 1:4 [3]. The most frequent location of teratoma in children is the sacrococcygeal area [4]. Many sacrococcygeal teratoma cases are diagnosed prenatally with routine ultrasonography between the 22nd and the 34th week of gestation. However, access to routine prenatal ultrasound in low and middle income countries is limited [5]. Antenatal diagnosis is essential to the pregnancy management and to prevent neonatal death by identifying fetuses that are at a higher risk of complications and planning an adequate intervention when needed [6]. This case is reported to describe a North African neonate presenting with a sacrococcygeal teratoma at birth without prior antenatal diagnosis, and highlight the need for prenatal routine care in low and middle income countries.
abstract_unstemmed	Sacrococcygeal teratomas (SCTs) are rare congenital tumors that are derived from embryonic germ cell layers [1]. They are the most common extragonadal germ cell tumors (GCTs) in the neonate, with a reported incidence of 1 in 35 000 births [2]. Teratomas are made of tissues that derive from three germinal layers (ectoderm, endoderm, and mesoderm). Sacrococcygeal teratomas are more common in girls, with a sex ratio of 1:4 [3]. The most frequent location of teratoma in children is the sacrococcygeal area [4]. Many sacrococcygeal teratoma cases are diagnosed prenatally with routine ultrasonography between the 22nd and the 34th week of gestation. However, access to routine prenatal ultrasound in low and middle income countries is limited [5]. Antenatal diagnosis is essential to the pregnancy management and to prevent neonatal death by identifying fetuses that are at a higher risk of complications and planning an adequate intervention when needed [6]. This case is reported to describe a North African neonate presenting with a sacrococcygeal teratoma at birth without prior antenatal diagnosis, and highlight the need for prenatal routine care in low and middle income countries.
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title_short	Mature ruptured sacrococcygeal teratoma in a 1-day old neonate
url	https://doi.org/10.1016/j.epsc.2022.102245 https://doaj.org/article/59b8d8e486884c8fbc6fdc71354c132d http://www.sciencedirect.com/science/article/pii/S2213576622000720 https://doaj.org/toc/2213-5766
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Mature ruptured sacrococcygeal teratoma in a 1-day old neonate

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