scholarly journals NS-04A CASE REPORT OF A GIANT CONGENITAL TERATOMA MANAGED THROUGH EX UTERO INTRAPARTUM TREATMENT PROCEDURE AND MULTIPLE STAGED SURGERIES

2016 ◽  
Vol 18 (suppl 3) ◽  
pp. iii127.4-iii127
Author(s):  
Ulrika Sandvik ◽  
Caroline Gahm ◽  
Georgios Papatziamos ◽  
Andreas Ekborn ◽  
Erik Neovius ◽  
...  
2014 ◽  
Vol 40 (8) ◽  
pp. 2005-2009 ◽  
Author(s):  
Masanori Suenaga ◽  
Nobuhiro Hidaka ◽  
Saki Kido ◽  
Yuka Otera ◽  
Kotaro Fukushima ◽  
...  

2017 ◽  
Vol 96 (1) ◽  
pp. E37-E40
Author(s):  
Todd J. Wannemuehler ◽  
Christopher R. Deig ◽  
Brandon P. Brown ◽  
Stuart A. Morgenstein

An ex utero intrapartum treatment procedure was performed to deliver a fetus with a multiseptated, entirely cystic, 4.5 × 5.0 × 4.0-cm mass occupying the oropharynx and oral cavity with protrusion from the mouth. Surgical excision was performed, and final pathologic diagnosis revealed a lymphatic malformation arising within a cystic oropharyngeal teratoma. Lymphatic malformations are virtually indistinguishable radiologically from rare, purely cystic teratomata, and efforts have been made to distinguish between the two in utero because of differing available treatment modalities. This represents the first documented case in the literature of a lymphatic malformation arising from within an oropharyngeal teratoma.


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Jerzy Stanek

AbstractShort CommunicationsEXIT (ex-utero intrapartum treatment) procedure is a fetal survival-increasing modification of cesarean section. Previously we found an increase incidence of fetal vascular malperfusion (FVM) in placentas from EXIT procedures which indicates the underlying stasis of fetal blood flow in such cases. This retrospective analysis analyzes the impact of the recently introduced CD34 immunostain for the FVM diagnosis in placentas from EXIT procedures.Objectives and MethodsA total of 105 placentas from EXIT procedures (48 to airway, 43 to ECMO and 14 to resection) were studied. In 73 older cases, the placental histological diagnosis of segmental FVM was made on H&E stained placental sections only (segmental villous avascularity) (Group 1), while in 32 most recent cases, the CD34 component of a double E-cadherin/CD34 immunostain slides was also routinely used to detect the early FVM (endothelial fragmentation, villous hypovascularity) (Group 2). 23 clinical and 47 independent placental phenotypes were compared by χ2 or ANOVA, where appropriate.ResultsThere was no statistical significance between the groups in rates of segmental villous avascularity (29 vs. 34%), but performing CD34 immunostain resulted in adding and/or upgrading 12 more cases of segmental FVM in Group 2, thus increasing the sensitivity of placental examination for FVM by 37%. There were no other statistically significantly differences in clinical (except for congenital diaphragmatic hernias statistically significantly more common in Group 2, 34 vs 56%, p=0.03) and placental phenotypes, proving the otherwise comparability of the groups.ConclusionsThe use of CD34 immunostain increases the sensitivity of placental examination for FVM by 1/3, which may improve the neonatal management by revealing the increased likelihood of the potentially life-threatening neonatal complications.


Author(s):  
Rakesh Srivastava ◽  
Vini Tandon

<p class="abstract">Teratomas are embryonal neoplasm arises from totipotent germ cells. They are having tissues from all the three blastodermic layers. There are various locations of congenital teratoma. Naso-oropharyngeal site teratoma are either sessile or pedunculated. We describe a rare case of laryngeal teratoma in a five years old patient presented with change in voice and breathing difficulty. On flexible laryngoscopy, it appeared like supraglottic cyst but on CT scan it was confirmed as teratoma. Pre-operative tracheostomy and transoral carbon dioxide laser assisted excision done. Histopathological examination showed osteoid trabeculae, chondroid tissue with loose myxoid islands and adipose tissue. No recurrence of tumor on 18 months follow-up. This is the first case report of pediatric larynx teratoma reported in present century.</p>


1999 ◽  
Vol 93 (Supplement) ◽  
pp. 824-825
Author(s):  
Kenneth W. Liechty ◽  
Timothy M. Crombleholme ◽  
Stuart Weiner ◽  
Brian Bernick ◽  
Alan W. Flake ◽  
...  

2008 ◽  
Vol 107 (9) ◽  
pp. 745-748 ◽  
Author(s):  
Hsin-Hui Chiu ◽  
Wei-Chung Hsu ◽  
Jin-Chung Shih ◽  
Po-Nien Tsao ◽  
Wu-Shiun Hsieh ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document