Perinatal evolution of mesenchymal hamartoma of the chest wall

Braatz Bastian, Rachel Evans, Anthony Kelman, Wei Cheng

Research output: Contribution to journalArticleResearchpeer-review

Abstract

Mesenchymal hamartoma of the chest wall (MHCW) is a rare condition. Previously, surgical resection has been advocated with considerable post-operative morbidity. Evidence for conservative management is lacking because the natural history of MHCW is unknown. We present serial measurements of an antenatally detected MHCW (8 antenatal ultrasounds and 2 postnatal computed tomographic scans). The study demonstrates that the relative tumor size peaked at birth and then decreased postnatally. Based on this evidence, we believe that MHCW can be managed conservatively in an asymptomatic patient.
Original languageEnglish
Pages (from-to)e37 - e40
Number of pages4
JournalJournal of Pediatric Surgery
Volume45
Issue number12
DOIs
Publication statusPublished - 2010

Cite this

Bastian, Braatz ; Evans, Rachel ; Kelman, Anthony ; Cheng, Wei. / Perinatal evolution of mesenchymal hamartoma of the chest wall. In: Journal of Pediatric Surgery. 2010 ; Vol. 45, No. 12. pp. e37 - e40.
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Perinatal evolution of mesenchymal hamartoma of the chest wall. / Bastian, Braatz; Evans, Rachel; Kelman, Anthony; Cheng, Wei.

In: Journal of Pediatric Surgery, Vol. 45, No. 12, 2010, p. e37 - e40.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

T1 - Perinatal evolution of mesenchymal hamartoma of the chest wall

AU - Bastian, Braatz

AU - Evans, Rachel

AU - Kelman, Anthony

AU - Cheng, Wei

PY - 2010

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N2 - Mesenchymal hamartoma of the chest wall (MHCW) is a rare condition. Previously, surgical resection has been advocated with considerable post-operative morbidity. Evidence for conservative management is lacking because the natural history of MHCW is unknown. We present serial measurements of an antenatally detected MHCW (8 antenatal ultrasounds and 2 postnatal computed tomographic scans). The study demonstrates that the relative tumor size peaked at birth and then decreased postnatally. Based on this evidence, we believe that MHCW can be managed conservatively in an asymptomatic patient.

AB - Mesenchymal hamartoma of the chest wall (MHCW) is a rare condition. Previously, surgical resection has been advocated with considerable post-operative morbidity. Evidence for conservative management is lacking because the natural history of MHCW is unknown. We present serial measurements of an antenatally detected MHCW (8 antenatal ultrasounds and 2 postnatal computed tomographic scans). The study demonstrates that the relative tumor size peaked at birth and then decreased postnatally. Based on this evidence, we believe that MHCW can be managed conservatively in an asymptomatic patient.

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DO - 10.1016/j.jpedsurg.2010.08.057

M3 - Article

VL - 45

SP - e37 - e40

JO - Journal of Pediatric Surgery

JF - Journal of Pediatric Surgery

SN - 0022-3468

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