scholarly journals Prenatal diagnosis and follow-up of giant sacrococcygeal teratoma: a case report

2018 ◽  
Vol 26 (1) ◽  
pp. 46-50
Author(s):  
Mucize Eriç Özdemir, ◽  
Oya Demirci ◽  
Güher Bolat ◽  
Ayşenur Celayir ◽  
Suna Cesur
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Sacrococcygeal Teratoma

Prenatal diagnosis of acute bladder distension associated with fetal sacrococcygeal teratoma—a case report

1995 ◽  
Vol 15 (12) ◽  
pp. 1160-1164 ◽  
Author(s):  
U. Elchalal ◽  
I. Ben-Shachar ◽  
M. Nadjari ◽  
E. Gross ◽  
Z. Appleman ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Sacrococcygeal Teratoma ◽  
Bladder Distension

Prenatal diagnosis and follow up of congenital splenic cyst: a case report

2001 ◽  
Vol 17 (5) ◽  
pp. 439-441 ◽  
Author(s):  
M. A. B. Lopes ◽  
R. Ruano ◽  
V. Bunduki ◽  
S. Miyadahira ◽  
M. Zugaib
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Splenic Cyst

Prenatal diagnosis of a de novo trisomy 6q22.2→6qter and monosomy lpter→1p36.3. Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q

2008 ◽  
Vol 51 (2) ◽  
pp. 115-117 ◽  
Author(s):  
Anita S. Kulharya ◽  
Mary E. Carlin ◽  
William A. Stettler ◽  
Martine Huslig ◽  
Mary K. Kukolich ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
De Novo ◽  
Partial Trisomy

scholarly journals Isolated Double Aortic Arch (Daa) – Prenatal Detection with Postnatal Follow-Up, Case Report and Literature Review

2018 ◽  
Vol 8 (1) ◽  
pp. 64-70
Author(s):  
Julia Murlewska ◽  
Agnieszka Żalińska ◽  
Danuta Roik ◽  
Bożena Werner ◽  
Maria Respondek-Liberska
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Literature Review ◽  
Aortic Arch ◽  
Clinical Symptoms ◽  
Double Aortic Arch ◽  
Computer Reconstruction ◽  
Prenatal Detection ◽  
Angio Ct

Abstract This case report presents a prenatal diagnosis with postnatal confirmation (by angio CT and computer reconstruction) of an isolated double aortic arch, with no blood disturbances and with no clinical symptoms after birth. Literature review was focusing on the possible symptoms in the future. Prenatal findings should be forwarded to neonatologist and pediatrician despite clinical silence.

scholarly journals Prenatal diagnosis and follow-up of giant sacrococcygeal teratoma

2011 ◽  
Vol 50 (2) ◽  
pp. 242-244 ◽  
Author(s):  
Esra Aktepe Keskin ◽  
Yuksel Arikan Onaran ◽  
Aysel Derbent ◽  
Aylin Ayrim ◽  
Hasan Kafali
Keyword(s):  
Prenatal Diagnosis ◽  
Sacrococcygeal Teratoma

scholarly journals P04.11: Prenatal diagnosis of tethered spinal cord associated with sacrococcygeal teratoma: a case report

2014 ◽  
Vol 44 (S1) ◽  
pp. 204-204
Author(s):  
T. Sarac Sivrikoz ◽  
R. Has ◽  
I.H. Kalelioglu ◽  
A. Corbacioglu Esmer ◽  
H. Kayserili ◽  
...  
Keyword(s):  
Spinal Cord ◽  
Case Report ◽  
Prenatal Diagnosis ◽  
Sacrococcygeal Teratoma ◽  
Tethered Spinal Cord

scholarly journals Adams-Oliver syndrome: Case report

2011 ◽  
Vol 139 (3-4) ◽  
pp. 221-224
Author(s):  
Vladimir Kuburovic ◽  
Vladislav Vukomanovic ◽  
Jovan Kosutic ◽  
Sanja Rakic ◽  
Slobodan Gazikalovic ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Clinical Features ◽  
Ultrasound Examination ◽  
Foramen Ovale ◽  
Limb Defects ◽  
Limb Reduction ◽  
Congenital Aplasia ◽  
The Right

Introduction. Adams-Oliver syndrome is characterized by congenital aplasia of the vertex skin of the skull in combination with skull and transverse limb defects. Case Outline. We presented a 5-month old female infant with Adams-Oliver syndrome manifested as cutis marmorata, dilated scalp veins and limb reduction defects. Clinical manifestation also included thumb hypoplasia and extreme hypoplasia of other fingers, with agenesis of all toes on both feet. Echocardiogram revealed foramen ovale apertum. Venography showed dilated malformed scalp and neck veins, predominantly on the right side. On the basis of the clinical features and extended investigation we confirmed Adams-Oliver syndrome in the presented patient. Conclusion. We recommended prenatal diagnosis in case of future pregnancies, ultrasound examination, and follow-up of foetal anomalies.

scholarly journals A CASE REPORT: PRENATAL DIAGNOSIS OF FETAL CARDIAC RHABDOMYOMA

2021 ◽  
Vol 5 (3) ◽  
Author(s):  
Tan Kui Foung ◽  
Mohd Aznan Md. Aris ◽  
Norhayaty Sharman Khamis Roslee
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Rare Disease ◽  
Cardiac Rhabdomyoma ◽  
Antenatal Ultrasound ◽  
Paediatric Cardiologist ◽  
Round Shape ◽  
Antenatal Ultrasonography

Fetal cardiac rhabdomyoma is a rare disease, and most of the cases are detected incidentally during the antenatal ultrasound. This is a case discovered during antenatal ultrasonography at 29 weeks of gestation. Multiple hyperechoic round shape masses were seen in the cardiac. After birth, the baby had been under a paediatric cardiologist follow-up with regular echocardiography. Management was mainly conservative at the time being as there was no sign of obstruction.

scholarly journals Prenatal diagnosis of granular cell myoblastoma: A case report

2006 ◽  
Vol 59 (11-12) ◽  
pp. 573-576
Author(s):  
Aleksandra Novakov-Mikic ◽  
Ljiljana Ivanovic ◽  
Milos Lucic ◽  
Aleksandar Kiralj ◽  
Katarina Koprivsek ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Oral Cavity ◽  
Cesarean Section ◽  
Amniotic Fluid ◽  
Granular Cell ◽  
Histopathological Diagnosis ◽  
Normal Female ◽  
Granular Cell Myoblastoma

Introduction. The aim of this paper is to present a case of prenatal diagnosis of a congenital tumor of the oral cavity diagnosed at 28 weeks of gestation. Case report. After the diagnosis of oral cavity tumor was made by 2D ultrasound, a 3D scan was performed, which confirmed the diagnosis revealing a peduncle at the upper border of maxilla. A detailed scan was performed and no additional anomalies were seen. Magnetic resonance imaging was performed, confirming the diagnosis and the site of the tumor. Karyotype was previously done, and a normal female karyotype was found. Regular three-week follow-up scans were performed to follow the growth of the tumor, as well as the state of the amniotic fluid. No tumor growth was detected, and the amniotic fluid volume was normal until 39 weeks of gestation. Cesarean section was scheduled, due to the risk of tumor disruption during a vaginal delivery. A maxillofacial surgeon was present during an uneventful cesarean section and a complete surgical excision was done immediately after the baby was extracted and umbilical cord ligated. The histopathological diagnosis was: granular cell myoblastoma. The female newborn was developing normally, and at 5 months of age there were no traces of scarring at the place of the tumor. Conclusion. In cases of prenatal diagnosis of tumors of the oral cavity, where development of polyhydramnios can be expected, as well as difficulties with feeding and breathing after birth, it is important to make a plan for adequate follow-up and prompt surgical treatment immediately after birth. .

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