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 Cystic Type IV Sacrococcygeal Teratoma

2002 ◽  
Vol 22 (4) ◽  
pp. 331-332 ◽  
Author(s):  
Thomas E Herman ◽  
Marilyn J Siegel
Keyword(s):  
Sacrococcygeal Teratoma ◽  
Type Iv ◽  
Cystic Type

scholarly journals Type IV Sacrococcygeal Teratoma Associated with Urogenital Sinus: Difficulties in the Prenatal Differential Diagnosis

2013 ◽  
Vol 2 (1) ◽  
pp. 9
Author(s):  
Zeki Şahinoğlu ◽  
Ayşenur Cerrah Celayir ◽  
Mehmet Reşit Asoglu ◽  
Nahit Özcan
Keyword(s):  
Differential Diagnosis ◽  
Pregnant Woman ◽  
Prenatal Diagnosis ◽  
Obstructive Uropathy ◽  
Cystic Mass ◽  
Urogenital Sinus ◽  
Sacrococcygeal Teratoma ◽  
Prenatal Ultrasonography ◽  
Type Iv ◽  
Renal Malformations

Sacrococcygeal teratoma (SCT) is being more often detected due to availability of prenatal ultrasonography. Type IV SCT could be misdiagnosed as cloacal abnormalities due to the pelvic midline cystic mass associated with renal malformations and obstructive uropathy during the pregnancy. We discuss difficulties in the prenatal differential diagnosis of SCT and urogenital sinus in a 26-year-old pregnant woman, admitted to our prenatal diagnosis centre for a detailed US for a pre-sacral mass.

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

Intra-abdominal (Type IV) sacrococcygeal teratoma presenting with buttock hemangioma

2013 ◽  
Vol 29 (12) ◽  
pp. 1341-1344 ◽  
Author(s):  
Siavash Raigani ◽  
Dimitris Agamanolis ◽  
Oliver S. Soldes ◽  
Todd A. Ponsky
Keyword(s):  
Sacrococcygeal Teratoma ◽  
Type Iv

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 Type IV Sacrococcygeal Teratoma Displacing the Urinary Bladder: Unique Magnetic Resonance Imaging

2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Sahar Eftekharzadeh ◽  
Sorena Keihani ◽  
Mehdi Fareghi ◽  
Alireza Alamsahebpour ◽  
Abdol-Mohammad Kajbafzadeh
Keyword(s):  
Magnetic Resonance ◽  
Wide Spectrum ◽  
Signs And Symptoms ◽  
Bowel Function ◽  
Mass Effect ◽  
Sacrococcygeal Teratoma ◽  
Voiding Function ◽  
Pediatric Tumor ◽  
Type Iv ◽  
External Component

Type IV sacrococcygeal teratoma is a rare pediatric tumor that is confined to the presacral area with no external component. The signs and symptoms often arise due to mass effect and compression of adjacent organs. Urinary retention is an uncommon presenting symptom in these patients. A wide spectrum of imaging findings may be encountered in cases with sacrococcygeal teratoma because of variability of tumor size and components. We hereby present a unique magnetic resonance urography finding in a type IV sacrococcygeal teratoma which caused bladder displacement. A meticulous and complete resection of tumor with special attention to the pelvic plexus led to preservation of normal voiding function and normal bowel function in this patient.

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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