scholarly journals Prenatal 3D-ultrasound diagnosis of isolated intrahepatic portal-systemic shunt with intact ductus venosus: A case report and literature review

2021 ◽  
Vol 16 (5) ◽  
pp. 1173-1178
Author(s):  
Maxime Van Houdt ◽  
Johannes van der Merwe ◽  
Marc Gewillig ◽  
Luc De Catte
Keyword(s):  
Case Report ◽  
Literature Review ◽  
3D Ultrasound ◽  
Ultrasound Diagnosis ◽  
Ductus Venosus ◽  
Portal Systemic Shunt

scholarly journals Three-dimensional ultrasound and HDlive in tubal serous cystadenofibroma: a case report and literature review

2017 ◽  
Vol 19 (4) ◽  
pp. 444 ◽  
Author(s):  
Mihaela Grigore ◽  
Razvan Popovici ◽  
Cristina Furnica ◽  
Anda Pristavu ◽  
Alexandru Hamod ◽  
...  
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Laparoscopic Surgery ◽  
Literature Review ◽  
Three Dimensional ◽  
3D Ultrasound ◽  
Chronic Abdominal Pain ◽  
Benign Tumors ◽  
Fallopian Tubes ◽  
Almost All

Cystadenofibromas of the fallopian tubes are very rare benign tumors and very few cases have been reported in the literature worldwide. Usually, the tumor is asymptomatic, and for almost all cases reported, the tumors were incidentally discovered during surgery for other genital pathology. We report the case of a 30-year-old woman with a serous cystadenofibroma of the fallopian tube, presenting with chronic abdominal pain and secondary infertility. The diagnosis of tubal tumor was formulated before surgery and confirmed during laparoscopic surgery. Both 3D ultrasound and HDlive were useful tools for the diagnosis. The ultrasound diagnosis was helpful in planning appropriate surgical management.

Prenatal 2D and 3D ultrasound diagnosis of diprosopus: case report with post-mortem magnetic resonance images (MRI) and review of the literature

2009 ◽  
Vol 29 (10) ◽  
pp. 992-994 ◽  
Author(s):  
Giuseppe Maria Maruotti ◽  
Dario Paladini ◽  
Raffaele Napolitano ◽  
Laura Letizia Mazzarelli ◽  
Tiziana Russo ◽  
...  
Keyword(s):  
Case Report ◽  
Magnetic Resonance ◽  
3D Ultrasound ◽  
Magnetic Resonance Images ◽  
Ultrasound Diagnosis ◽  
Post Mortem ◽  
Review Of The Literature ◽  
2D And 3D

Synovial Chondromatosis: Case Report and Literature Review of a Rare Ultrasound Diagnosis

2013 ◽  
Vol 39 (5) ◽  
pp. S54
Author(s):  
B. Maragno ◽  
M.C.N.A. Leite ◽  
N.C.M.F. Montenegro ◽  
N.B. Genova ◽  
C.A. Sinisgalli
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Synovial Chondromatosis ◽  
Ultrasound Diagnosis

scholarly journals P44.04: Beckwith-Wiedemann Syndrome: prenatal 2D and 3D ultrasound diagnosis: case report

2007 ◽  
Vol 30 (4) ◽  
pp. 619-619
Author(s):  
C. Simioni ◽  
P. M. Nowak ◽  
W. J. Hisaba ◽  
L. M. M. Nardozza ◽  
A. F. Moron
Keyword(s):  
Case Report ◽  
3D Ultrasound ◽  
Ultrasound Diagnosis ◽  
2D And 3D

EP03.09: Prenatal 3D ultrasound diagnosis of vein of Galen aneurysm (VGAM): case report

2015 ◽  
Vol 46 ◽  
pp. 193-193
Author(s):  
M.J. Kudla ◽  
A. Beczkowska-Kielek ◽  
K. Kutta
Keyword(s):  
Case Report ◽  
3D Ultrasound ◽  
Ultrasound Diagnosis ◽  
Vein Of Galen ◽  
Vein Of Galen Aneurysm

scholarly journals A Silent Congenital Ethmoidal Encephalocele Progressing into Frontoethmoidal Meningoencephalocele with Episodic Seizures in Adulthood: A Case Report and Literature Review

2018 ◽  
Vol 6 (3) ◽  
pp. 20
Author(s):  
Xiang Yang ◽  
Xiaolin Ai ◽  
Seidu A. Richard ◽  
Jianguo Xu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Ct Scan ◽  
Congenital Malformations ◽  
3D Ultrasound ◽  
Ultrasound Scan ◽  
Skull Defect ◽  
Nasal Bridge ◽  
Case Presentation ◽  
High Incidence

Background: Frontoethmoidal meningoencephalocele (FEM) is rare congenital malformations that has specific geographic distribution. This condition is depicted with herniation of brain tissue as well as meninges via a defect in the cranium at the frontal, orbital, nasal as well as ethmoidal regions. Although several cases have been reported, none of them have a silent and progressive nature with episodic seizures. Case Presentation: We present a 20-year-old man with a swelling on the nasal bridge which was notice a few years after birth. The swelling initially progressed slowly without any symptoms from childhood through adolescents. Both CT scan and MRI revealed a defect in cranium at the frontal and ethmoidal regions with herniation of meninges and brain matter into the nasal cavity but no fistula. We successfully reduced the encephalocele as well as watertight closed the dura mater. The skull defect repaired, and left orbital defect also reconstructed via surgery. Conclusions: Aflatoxins, generated by one genus of a defective fungi, aspergillus could be responsible for the development of this malformation. We suggest that pregnant women in areas with high incidence of the malformation be screen thorough with ultrasound scan to detect the malformation earlier. We also suggest that further studies on the malformation be geared toward using 3D ultrasound to study the pathophysiology of this malformation.

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