Sacrococcygeal teratoma over two decades: Birth prevalence, prenatal diagnosis and clinical outcomes

2008 ◽  
Vol 28 (11) ◽  
pp. 1048-1051 ◽  
Author(s):  
Ravi Swamy ◽  
Nicholas Embleton ◽  
Juliet Hale
Keyword(s):  
Prenatal Diagnosis ◽  
Clinical Outcomes ◽  
Sacrococcygeal Teratoma ◽  
Birth Prevalence

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 of sacrococcygeal teratoma

1979 ◽  
Vol 134 (2) ◽  
pp. 228-229 ◽  
Author(s):  
Edgar O. Horger ◽  
Linda M. McCarter
Keyword(s):  
Prenatal Diagnosis ◽  
Sacrococcygeal Teratoma

Prenatal diagnosis of a cystic type IV sacrococcygeal teratoma mimicking a cloacal anomaly: contribution of MR

2005 ◽  
Vol 25 (3) ◽  
pp. 216-219 ◽  
Author(s):  
C. Garel ◽  
L. Mizouni ◽  
F. Menez ◽  
D. Luton ◽  
D. Guibourdenche ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Sacrococcygeal Teratoma ◽  
Type Iv ◽  
Cloacal Anomaly ◽  
Cystic Type

scholarly journals Clinical outcomes of prenatal diagnosis of the fetal micrognathia

Medicine ◽  
2020 ◽  
Vol 99 (4) ◽  
pp. e18648
Author(s):  
Jin-Wen Lu ◽  
Dan Lu ◽  
Xiao-Li Zhang ◽  
Jiao Bai
Keyword(s):  
Prenatal Diagnosis ◽  
Clinical Outcomes

Sacrococcygeal teratoma in children: Audit on clinical outcomes from a single centre

2019 ◽  
Vol 18 (4) ◽  
pp. 26
Author(s):  
O. Nasher ◽  
M.R. Powis ◽  
R. Squire ◽  
B. Lakshminarayanan
Keyword(s):  
Clinical Outcomes ◽  
Sacrococcygeal Teratoma ◽  
Single Centre

Ring chromosome 21 presenting with sacrococcygeal teratoma: Prenatal diagnosis, molecular cytogenetic characterization and literature review

Gene ◽  
2013 ◽  
Vol 522 (1) ◽  
pp. 111-116 ◽  
Author(s):  
Chih-Ping Chen ◽  
Po-Jen Cheng ◽  
Shuenn-Dyh Chang ◽  
Yi-Xuan Lee ◽  
Jin-Chung Shih ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Literature Review ◽  
Ring Chromosome ◽  
Chromosome 21 ◽  
Sacrococcygeal Teratoma ◽  
Molecular Cytogenetic ◽  
Cytogenetic Characterization

scholarly journals Two Neonates with Congenital Hydrocolpos

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Vydehi Murthy ◽  
Jessica Costalez ◽  
Julie Weiner ◽  
Kristin Voos
Keyword(s):  
Prenatal Diagnosis ◽  
Reproductive Tract ◽  
Abdominal Mass ◽  
Rare Condition ◽  
Mass Effect ◽  
Cystic Mass ◽  
Sacrococcygeal Teratoma ◽  
Mri Imaging ◽  
Fetal Diagnosis ◽  
High Index Of Suspicion

Introduction. Neonatal hydrocolpos is a rare condition. Hydrocolpos is cystic dilatation of the vagina with fluid accumulation due to a combination of stimulation of secretary glands of the reproductive tract and vaginal obstruction. The differential for a neonatal presentation of lower abdominal mass includes urogenital anomalies, Hirschsprung’s, disease or sacrococcygeal teratoma. Prenatal diagnosis and early newborn imaging studies leads to early detection and treatment of these cases.Case. We report here two cases of neonatal hydrocolpos with prenatal diagnosis of lower abdominal mass. Postnatally, ultrasound, MRI imaging, and cystoscopy confirmed large cystic mass as hydrocolpos with distal vaginal obstruction. Both patients had enlarged renal system secondary to mass effect.Conclusion. High index of suspicion for hydrocolpos in a newborn presenting with fetal diagnosis of infraumbilical abdominal mass will facilitate timely intervention and prevention of complications.

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