Antenatal diagnosis of congenital hepatic hemangioma: a case report

Abstract Hepatic tumors in children account for only 1 to 5% of all pediatric tumors. Hepatic hemangioma is, however, the third most common tumor of the liver in childhood. We report a case of an antenatal diagnosis of a hepatic tumor detected on a first obstetric ultrasound, at $ 26^{th} $ week of...
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Autor*in:	Cabrita, Sofia Vargas [verfasserIn] Gonçalves, Sónia Rodrigues, Henrique Guerra, Nuno Moura, Paulo

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2009

Schlagwörter:	Hemangioma Infantile Hemangioma Hepatic Hemangioma Obstetric Ultrasound Doppler Blood Flow

Anmerkung:	© licensee BioMed Central Ltd. 2009. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (

Übergeordnetes Werk:	Enthalten in: Cases journal - London : Biomed Central, 2008, 2(2009), 1 vom: 07. Aug.
Übergeordnetes Werk:	volume:2 ; year:2009 ; number:1 ; day:07 ; month:08

Links:	Volltext

DOI / URN:	10.4076/1757-1626-2-6829

Katalog-ID:	SPR031091067

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520			\|a Abstract Hepatic tumors in children account for only 1 to 5% of all pediatric tumors. Hepatic hemangioma is, however, the third most common tumor of the liver in childhood. We report a case of an antenatal diagnosis of a hepatic tumor detected on a first obstetric ultrasound, at $ 26^{th} $ week of gestation. It revealed a complex, predominantly solid hepatic lesion with 3 × 3 cm and a marked, essentially peripheral, Doppler blood flow. Fetal echocardiography showed a normal heart besides a vena cava displacement by the hepatic mass. Fetal Hepatic hemangioma was suspected. Follow-up ultrasounds were unchanged. Pregnancy evolved well. At 36 weeks of gestation was spontaneously delivered a 3300 g boy whose examination revealed a visible thoracoabdominal circulation and a palpable liver. No skin lesions, namely hemangiomas or petechiae were identified. Postnatal magnetic resonance imaging confirmed the diagnosis of Hepatic hemangioma. Treatment was initiated with prednisolone followed by interferon. After 2 years, there is no active lesion.
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spelling	10.4076/1757-1626-2-6829 doi (DE-627)SPR031091067 (SPR)1757-1626-2-6829-e DE-627 ger DE-627 rakwb eng Cabrita, Sofia Vargas verfasserin aut Antenatal diagnosis of congenital hepatic hemangioma: a case report 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © licensee BioMed Central Ltd. 2009. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Abstract Hepatic tumors in children account for only 1 to 5% of all pediatric tumors. Hepatic hemangioma is, however, the third most common tumor of the liver in childhood. We report a case of an antenatal diagnosis of a hepatic tumor detected on a first obstetric ultrasound, at $ 26^{th} $ week of gestation. It revealed a complex, predominantly solid hepatic lesion with 3 × 3 cm and a marked, essentially peripheral, Doppler blood flow. Fetal echocardiography showed a normal heart besides a vena cava displacement by the hepatic mass. Fetal Hepatic hemangioma was suspected. Follow-up ultrasounds were unchanged. Pregnancy evolved well. At 36 weeks of gestation was spontaneously delivered a 3300 g boy whose examination revealed a visible thoracoabdominal circulation and a palpable liver. No skin lesions, namely hemangiomas or petechiae were identified. Postnatal magnetic resonance imaging confirmed the diagnosis of Hepatic hemangioma. Treatment was initiated with prednisolone followed by interferon. After 2 years, there is no active lesion. Hemangioma (dpeaa)DE-He213 Infantile Hemangioma (dpeaa)DE-He213 Hepatic Hemangioma (dpeaa)DE-He213 Obstetric Ultrasound (dpeaa)DE-He213 Doppler Blood Flow (dpeaa)DE-He213 Gonçalves, Sónia aut Rodrigues, Henrique aut Guerra, Nuno aut Moura, Paulo aut Enthalten in Cases journal London : Biomed Central, 2008 2(2009), 1 vom: 07. Aug. (DE-627)569611202 (DE-600)2431132-7 1757-1626 nnns volume:2 year:2009 number:1 day:07 month:08 https://dx.doi.org/10.4076/1757-1626-2-6829 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 2009 1 07 08
allfields_unstemmed	10.4076/1757-1626-2-6829 doi (DE-627)SPR031091067 (SPR)1757-1626-2-6829-e DE-627 ger DE-627 rakwb eng Cabrita, Sofia Vargas verfasserin aut Antenatal diagnosis of congenital hepatic hemangioma: a case report 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © licensee BioMed Central Ltd. 2009. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Abstract Hepatic tumors in children account for only 1 to 5% of all pediatric tumors. Hepatic hemangioma is, however, the third most common tumor of the liver in childhood. We report a case of an antenatal diagnosis of a hepatic tumor detected on a first obstetric ultrasound, at $ 26^{th} $ week of gestation. It revealed a complex, predominantly solid hepatic lesion with 3 × 3 cm and a marked, essentially peripheral, Doppler blood flow. Fetal echocardiography showed a normal heart besides a vena cava displacement by the hepatic mass. Fetal Hepatic hemangioma was suspected. Follow-up ultrasounds were unchanged. Pregnancy evolved well. At 36 weeks of gestation was spontaneously delivered a 3300 g boy whose examination revealed a visible thoracoabdominal circulation and a palpable liver. No skin lesions, namely hemangiomas or petechiae were identified. Postnatal magnetic resonance imaging confirmed the diagnosis of Hepatic hemangioma. Treatment was initiated with prednisolone followed by interferon. After 2 years, there is no active lesion. Hemangioma (dpeaa)DE-He213 Infantile Hemangioma (dpeaa)DE-He213 Hepatic Hemangioma (dpeaa)DE-He213 Obstetric Ultrasound (dpeaa)DE-He213 Doppler Blood Flow (dpeaa)DE-He213 Gonçalves, Sónia aut Rodrigues, Henrique aut Guerra, Nuno aut Moura, Paulo aut Enthalten in Cases journal London : Biomed Central, 2008 2(2009), 1 vom: 07. Aug. (DE-627)569611202 (DE-600)2431132-7 1757-1626 nnns volume:2 year:2009 number:1 day:07 month:08 https://dx.doi.org/10.4076/1757-1626-2-6829 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 2009 1 07 08
allfieldsGer	10.4076/1757-1626-2-6829 doi (DE-627)SPR031091067 (SPR)1757-1626-2-6829-e DE-627 ger DE-627 rakwb eng Cabrita, Sofia Vargas verfasserin aut Antenatal diagnosis of congenital hepatic hemangioma: a case report 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © licensee BioMed Central Ltd. 2009. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Abstract Hepatic tumors in children account for only 1 to 5% of all pediatric tumors. Hepatic hemangioma is, however, the third most common tumor of the liver in childhood. We report a case of an antenatal diagnosis of a hepatic tumor detected on a first obstetric ultrasound, at $ 26^{th} $ week of gestation. It revealed a complex, predominantly solid hepatic lesion with 3 × 3 cm and a marked, essentially peripheral, Doppler blood flow. Fetal echocardiography showed a normal heart besides a vena cava displacement by the hepatic mass. Fetal Hepatic hemangioma was suspected. Follow-up ultrasounds were unchanged. Pregnancy evolved well. At 36 weeks of gestation was spontaneously delivered a 3300 g boy whose examination revealed a visible thoracoabdominal circulation and a palpable liver. No skin lesions, namely hemangiomas or petechiae were identified. Postnatal magnetic resonance imaging confirmed the diagnosis of Hepatic hemangioma. Treatment was initiated with prednisolone followed by interferon. After 2 years, there is no active lesion. Hemangioma (dpeaa)DE-He213 Infantile Hemangioma (dpeaa)DE-He213 Hepatic Hemangioma (dpeaa)DE-He213 Obstetric Ultrasound (dpeaa)DE-He213 Doppler Blood Flow (dpeaa)DE-He213 Gonçalves, Sónia aut Rodrigues, Henrique aut Guerra, Nuno aut Moura, Paulo aut Enthalten in Cases journal London : Biomed Central, 2008 2(2009), 1 vom: 07. Aug. (DE-627)569611202 (DE-600)2431132-7 1757-1626 nnns volume:2 year:2009 number:1 day:07 month:08 https://dx.doi.org/10.4076/1757-1626-2-6829 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 2009 1 07 08
allfieldsSound	10.4076/1757-1626-2-6829 doi (DE-627)SPR031091067 (SPR)1757-1626-2-6829-e DE-627 ger DE-627 rakwb eng Cabrita, Sofia Vargas verfasserin aut Antenatal diagnosis of congenital hepatic hemangioma: a case report 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © licensee BioMed Central Ltd. 2009. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Abstract Hepatic tumors in children account for only 1 to 5% of all pediatric tumors. Hepatic hemangioma is, however, the third most common tumor of the liver in childhood. We report a case of an antenatal diagnosis of a hepatic tumor detected on a first obstetric ultrasound, at $ 26^{th} $ week of gestation. It revealed a complex, predominantly solid hepatic lesion with 3 × 3 cm and a marked, essentially peripheral, Doppler blood flow. Fetal echocardiography showed a normal heart besides a vena cava displacement by the hepatic mass. Fetal Hepatic hemangioma was suspected. Follow-up ultrasounds were unchanged. Pregnancy evolved well. At 36 weeks of gestation was spontaneously delivered a 3300 g boy whose examination revealed a visible thoracoabdominal circulation and a palpable liver. No skin lesions, namely hemangiomas or petechiae were identified. Postnatal magnetic resonance imaging confirmed the diagnosis of Hepatic hemangioma. Treatment was initiated with prednisolone followed by interferon. After 2 years, there is no active lesion. Hemangioma (dpeaa)DE-He213 Infantile Hemangioma (dpeaa)DE-He213 Hepatic Hemangioma (dpeaa)DE-He213 Obstetric Ultrasound (dpeaa)DE-He213 Doppler Blood Flow (dpeaa)DE-He213 Gonçalves, Sónia aut Rodrigues, Henrique aut Guerra, Nuno aut Moura, Paulo aut Enthalten in Cases journal London : Biomed Central, 2008 2(2009), 1 vom: 07. Aug. (DE-627)569611202 (DE-600)2431132-7 1757-1626 nnns volume:2 year:2009 number:1 day:07 month:08 https://dx.doi.org/10.4076/1757-1626-2-6829 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 2009 1 07 08
language	English
source	Enthalten in Cases journal 2(2009), 1 vom: 07. Aug. volume:2 year:2009 number:1 day:07 month:08
sourceStr	Enthalten in Cases journal 2(2009), 1 vom: 07. Aug. volume:2 year:2009 number:1 day:07 month:08
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topic_facet	Hemangioma Infantile Hemangioma Hepatic Hemangioma Obstetric Ultrasound Doppler Blood Flow
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container_title	Cases journal
authorswithroles_txt_mv	Cabrita, Sofia Vargas @@aut@@ Gonçalves, Sónia @@aut@@ Rodrigues, Henrique @@aut@@ Guerra, Nuno @@aut@@ Moura, Paulo @@aut@@
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author	Cabrita, Sofia Vargas
spellingShingle	Cabrita, Sofia Vargas misc Hemangioma misc Infantile Hemangioma misc Hepatic Hemangioma misc Obstetric Ultrasound misc Doppler Blood Flow Antenatal diagnosis of congenital hepatic hemangioma: a case report
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topic_title	Antenatal diagnosis of congenital hepatic hemangioma: a case report Hemangioma (dpeaa)DE-He213 Infantile Hemangioma (dpeaa)DE-He213 Hepatic Hemangioma (dpeaa)DE-He213 Obstetric Ultrasound (dpeaa)DE-He213 Doppler Blood Flow (dpeaa)DE-He213
topic	misc Hemangioma misc Infantile Hemangioma misc Hepatic Hemangioma misc Obstetric Ultrasound misc Doppler Blood Flow
topic_unstemmed	misc Hemangioma misc Infantile Hemangioma misc Hepatic Hemangioma misc Obstetric Ultrasound misc Doppler Blood Flow
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title	Antenatal diagnosis of congenital hepatic hemangioma: a case report
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title_full	Antenatal diagnosis of congenital hepatic hemangioma: a case report
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title_sort	antenatal diagnosis of congenital hepatic hemangioma: a case report
title_auth	Antenatal diagnosis of congenital hepatic hemangioma: a case report
abstract	Abstract Hepatic tumors in children account for only 1 to 5% of all pediatric tumors. Hepatic hemangioma is, however, the third most common tumor of the liver in childhood. We report a case of an antenatal diagnosis of a hepatic tumor detected on a first obstetric ultrasound, at $ 26^{th} $ week of gestation. It revealed a complex, predominantly solid hepatic lesion with 3 × 3 cm and a marked, essentially peripheral, Doppler blood flow. Fetal echocardiography showed a normal heart besides a vena cava displacement by the hepatic mass. Fetal Hepatic hemangioma was suspected. Follow-up ultrasounds were unchanged. Pregnancy evolved well. At 36 weeks of gestation was spontaneously delivered a 3300 g boy whose examination revealed a visible thoracoabdominal circulation and a palpable liver. No skin lesions, namely hemangiomas or petechiae were identified. Postnatal magnetic resonance imaging confirmed the diagnosis of Hepatic hemangioma. Treatment was initiated with prednisolone followed by interferon. After 2 years, there is no active lesion. © licensee BioMed Central Ltd. 2009. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
abstractGer	Abstract Hepatic tumors in children account for only 1 to 5% of all pediatric tumors. Hepatic hemangioma is, however, the third most common tumor of the liver in childhood. We report a case of an antenatal diagnosis of a hepatic tumor detected on a first obstetric ultrasound, at $ 26^{th} $ week of gestation. It revealed a complex, predominantly solid hepatic lesion with 3 × 3 cm and a marked, essentially peripheral, Doppler blood flow. Fetal echocardiography showed a normal heart besides a vena cava displacement by the hepatic mass. Fetal Hepatic hemangioma was suspected. Follow-up ultrasounds were unchanged. Pregnancy evolved well. At 36 weeks of gestation was spontaneously delivered a 3300 g boy whose examination revealed a visible thoracoabdominal circulation and a palpable liver. No skin lesions, namely hemangiomas or petechiae were identified. Postnatal magnetic resonance imaging confirmed the diagnosis of Hepatic hemangioma. Treatment was initiated with prednisolone followed by interferon. After 2 years, there is no active lesion. © licensee BioMed Central Ltd. 2009. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
abstract_unstemmed	Abstract Hepatic tumors in children account for only 1 to 5% of all pediatric tumors. Hepatic hemangioma is, however, the third most common tumor of the liver in childhood. We report a case of an antenatal diagnosis of a hepatic tumor detected on a first obstetric ultrasound, at $ 26^{th} $ week of gestation. It revealed a complex, predominantly solid hepatic lesion with 3 × 3 cm and a marked, essentially peripheral, Doppler blood flow. Fetal echocardiography showed a normal heart besides a vena cava displacement by the hepatic mass. Fetal Hepatic hemangioma was suspected. Follow-up ultrasounds were unchanged. Pregnancy evolved well. At 36 weeks of gestation was spontaneously delivered a 3300 g boy whose examination revealed a visible thoracoabdominal circulation and a palpable liver. No skin lesions, namely hemangiomas or petechiae were identified. Postnatal magnetic resonance imaging confirmed the diagnosis of Hepatic hemangioma. Treatment was initiated with prednisolone followed by interferon. After 2 years, there is no active lesion. © licensee BioMed Central Ltd. 2009. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
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title_short	Antenatal diagnosis of congenital hepatic hemangioma: a case report
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