Three-step management of a newborn with a giant, highly vascularized, cervical teratoma: a case report.


Journal

Journal of medical case reports
ISSN: 1752-1947
Titre abrégé: J Med Case Rep
Pays: England
ID NLM: 101293382

Informations de publication

Date de publication:
10 Mar 2019
Historique:
received: 25 06 2018
accepted: 10 01 2019
entrez: 11 3 2019
pubmed: 11 3 2019
medline: 25 6 2019
Statut: epublish

Résumé

A giant congenital cervical teratoma is often highly vascularized; thus, in addition to a life-threatening airway occlusion at birth it comprises a high risk for significant and lethal blood loss during resection. In the case presented, an endovascular embolization of the carotid artery that supplied a giant congenital cervical teratoma was done as part of a three-stage treatment soon after birth and contributed to an overall good outcome. Embolization in cases of cervical teratomas was not described previously. We present a case of a preterm newborn from a Sephardic jewish origin with a giant, highly vascularized, congenital cervical teratoma that was managed successfully in three stages: (1) delivery by an ex utero intrapartum treatment procedure after extensive preoperative planning and followed by tracheostomy, (2) endovascular embolization of the carotid artery that supplied the tumor in order to decrease blood loss during resection, and (3) complete surgical resection. The parents were involved in all the ethical and medical decisions, starting just after the cervical mass was diagnosed prenatally. The management of giant congenital cervical teratoma is often challenging from both a medical and ethical prospective. Meticulous perinatal planning and parents' involvement is crucial. Endovascular embolization of the tumor feeding vessels can significantly improve the resection outcome and overall prognosis.

Sections du résumé

BACKGROUND BACKGROUND
A giant congenital cervical teratoma is often highly vascularized; thus, in addition to a life-threatening airway occlusion at birth it comprises a high risk for significant and lethal blood loss during resection. In the case presented, an endovascular embolization of the carotid artery that supplied a giant congenital cervical teratoma was done as part of a three-stage treatment soon after birth and contributed to an overall good outcome. Embolization in cases of cervical teratomas was not described previously.
CASE PRESENTATION METHODS
We present a case of a preterm newborn from a Sephardic jewish origin with a giant, highly vascularized, congenital cervical teratoma that was managed successfully in three stages: (1) delivery by an ex utero intrapartum treatment procedure after extensive preoperative planning and followed by tracheostomy, (2) endovascular embolization of the carotid artery that supplied the tumor in order to decrease blood loss during resection, and (3) complete surgical resection. The parents were involved in all the ethical and medical decisions, starting just after the cervical mass was diagnosed prenatally.
CONCLUSION CONCLUSIONS
The management of giant congenital cervical teratoma is often challenging from both a medical and ethical prospective. Meticulous perinatal planning and parents' involvement is crucial. Endovascular embolization of the tumor feeding vessels can significantly improve the resection outcome and overall prognosis.

Identifiants

pubmed: 30851737
doi: 10.1186/s13256-019-1976-0
pii: 10.1186/s13256-019-1976-0
pmc: PMC6409158
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

73

Références

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pubmed: 11034516
Int J Pediatr Otorhinolaryngol. 2002 Sep 24;65(3):241-7
pubmed: 12242140
Birth Defects Res A Clin Mol Teratol. 2005 Aug;73(8):572-6
pubmed: 16001440
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pubmed: 19416574
J Pediatr Surg. 2011 Jan;46(1):e5-8
pubmed: 21238631
J Pediatr Surg. 2011 May;46(5):817-22
pubmed: 21616233
J Clin Neonatol. 2013 Jan;2(1):42-5
pubmed: 24027746
Indian J Radiol Imaging. 2013 Apr;23(2):145-7
pubmed: 24082479

Auteurs

Ori Hochwald (O)

Neonatal Intensive Care Unit, Ruth Rappaport Children's Hospital, Rambam Health Campus, Haifa, Israel. Ori.inbal@gmail.com.

Ziv Gil (Z)

Department of Otolaryngology Head and Neck Surgery, Rambam Health Campus, Haifa, Israel.

Arie Gordin (A)

Department of Otolaryngology Head and Neck Surgery, Rambam Health Campus, Haifa, Israel.
The Pediatric ENT service, Rambam Health Campus, Haifa, Israel.

Zeev Winer (Z)

The Obstetrics & Gynecology Division, Rambam Health Campus, Haifa, Israel.

Ron Avrahami (R)

The Obstetrics & Gynecology Division, Rambam Health Campus, Haifa, Israel.

Eitan Abargel (E)

Invasive Neuroradiology Unit, Rambam Health Campus, Haifa, Israel.

Asaad Khoury (A)

Department of Pediatric Cardiology & Congenital Heart Disease in Adults, Ruth Rappaport Children's Hospital, Rambam Health Campus, Haifa, Israel.

Amit Lehavi (A)

The Department of Anesthesiology, Rambam Health Campus, Haifa, Israel.

Philippe Abecassis (P)

The Department of Anesthesiology, Rambam Health Campus, Haifa, Israel.

Liron Eldor (L)

The Department of Plastic Surgery, Rambam Health Campus, Haifa, Israel.

Ofer Ben-Izhak (O)

The Department of Pathology, Rambam Health Campus, Haifa, Israel.

Liron Borenstein-Levin (L)

Neonatal Intensive Care Unit, Ruth Rappaport Children's Hospital, Rambam Health Campus, Haifa, Israel.

Ran Stienberg (R)

The Department of Pediatric Surgery, Rambam Health Campus, Haifa, Israel.

Amir Kugelman (A)

Neonatal Intensive Care Unit, Ruth Rappaport Children's Hospital, Rambam Health Campus, Haifa, Israel.

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