Magnetic resonance imaging in the evaluation of uterus didelphys with obstructed hemivagina and renal agenesis: a case report

2006 ◽  
Vol 274 (4) ◽  
pp. 246-247 ◽  
Author(s):  
Ljiljana Mirkovic ◽  
Aleksandar Ljubic ◽  
Darko Mirkovic
Keyword(s):  
Magnetic Resonance Imaging ◽  
Case Report ◽  
Magnetic Resonance ◽  
Renal Agenesis ◽  
Resonance Imaging ◽  
Uterus Didelphys ◽  
Obstructed Hemivagina

scholarly journals Uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis

2007 ◽  
Vol 54 (3) ◽  
pp. 137-139 ◽  
Author(s):  
Lj. Mirkovic ◽  
D. Mirkovic ◽  
V. Boskovic ◽  
Z. Markovic
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Magnetic Resonance ◽  
Mr Imaging ◽  
Clinical Examination ◽  
Renal Agenesis ◽  
Clinical Manifestations ◽  
Uterus Didelphys ◽  
Rare Anomaly ◽  
Obstructed Hemivagina

This is a case report of two patients how have uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis with different clinical manifestations. Progressive abdominal pain after menarche, anuria or obstipation with the existing paravaginal tumor indicates this rare anomaly. Initially, the anomaly remains unrecognized, while patients most frequently referred to surgeons for assistance. The method of choice for diagnosis is clinical examination, ultrasonography and magnetic resonance (MR) imaging. Transvaginal excision of the septum is appropriate mode of treatment.

scholarly journals Herlyn-Werner-Wunderlich syndrome presenting with dysmenorrhea: a case report

2019 ◽  
Vol 13 (1) ◽  
Author(s):  
Dilruba Sharmen Nishu ◽  
Md. Monir Uddin ◽  
Khadija Akter ◽  
Shameema Akter ◽  
Monira Sarmin ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Abdominal Pain ◽  
Case Report ◽  
Magnetic Resonance ◽  
Magnetic Resonance Imaging Finding ◽  
Resonance Imaging ◽  
Pelvic Magnetic Resonance Imaging ◽  
Endometrial Cavity ◽  
Obstructed Hemivagina ◽  
The Right

Abstract Background Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. The most common presentation is abdominal pain, dysmenorrhea, and abdominal mass secondary to hematocolpos. We present the first case report on Herlyn-Werner-Wunderlich syndrome from Bangladesh. Case presentation A 15-year-old Asian girl presented with lower abdominal pain of 3 months’ duration. She had had menarche 3 months earlier and had a regular menstrual cycle with cyclical abdominal pain. Abdominal examination found a tender mass on the right iliac fossa. Further evaluation with ultrasound revealed distended endometrial cavity filled with complex fluid and nonvisualization of the right kidney. Pelvic magnetic resonance imaging showed absent right kidney and two separate endometrial stripes surrounded by endometrium and a muscular layer. The right endometrial cavity and cervix were distended with blood. This magnetic resonance imaging finding is consistent with Herlyn-Werner-Wunderlich syndrome with uterine didelphyis, right-sided hematometra resulting from obstructed hemivagina, and ipsilateral agenesis of the right kidney. The vaginal septum was resected for vaginoplasty. She was discharged 5 days after surgery and came for follow-up after 7 days. Vaginal examination revealed a healthy wound with no adhesion of the vaginal wall. She also informed us that she had started regular menstruation without any pain 30 days after the operation. Conclusion An unusual presentation of regular menstruation and nonspecific abdominal pain delays the diagnosis, which can lead to complications such as endometriosis and infertility. Awareness is required; otherwise, misdiagnosis clearly can occur.

scholarly journals Complementary role of magnetic resonance imaging after ultrasound examination in assessing fetal renal agenesis: a case report

2014 ◽  
Vol 8 (1) ◽  
Author(s):  
Tomasz Gęca ◽  
Arkadiusz Krzyżanowski ◽  
Aleksandra Stupak ◽  
Anna Kwaśniewska ◽  
Tomasz Pikuła ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Case Report ◽  
Magnetic Resonance ◽  
Renal Agenesis ◽  
Ultrasound Examination ◽  
Resonance Imaging ◽  
Complementary Role

scholarly journals Management of Hematometra in Single Horn of Didelphic Uterus with Obstructed Hemivagina and Ipsilateral Renal Agenesis Syndrome: A Case Report with Brief Review of Literature

2016 ◽  
Vol 8 (3) ◽  
pp. 231-235
Author(s):  
Ritu Agarwal
Keyword(s):  
Case Report ◽  
South Asian ◽  
Renal Agenesis ◽  
Rare Entity ◽  
Review Of Literature ◽  
Resonance Imaging ◽  
Uterus Didelphys ◽  
Future Fertility ◽  
Ohvira Syndrome ◽  
Obstructed Hemivagina

ABSTRACT The triad of uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis (OHVIRA) syndrome is a rare entity. These cases are difficult to diagnose due to heterogeneous presentation and rarity of the condition. Ultrasonography and magnetic resonance imaging are important for initial diagnosis; however, laparoscopy is required for the confirmation of the diagnosis. Early and accurate diagnosis of this condition followed by prompt surgical therapy is essential to prevent complications and to preserve future fertility. Here we report a case of uterus didelphys with hemivagina and ipsilateral renal agenesis with hematometra and hematosalpinx in a young girl. How to cite this article Mishra VV, Agarwal R, Bandwal P, Choudhary S, Gandhi K. Management of Hematometra in Single Horn of Didelphic Uterus with Obstructed Hemivagina and Ipsilateral Renal Agenesis Syndrome: A Case Report with Brief Review of Literature. J South Asian Feder Obst Gynae 2016;8(3):231-235.

Meningocerebral Angiodysplasia: Post-Mortem Magnetic Resonance Imaging and Autopsy

2009 ◽  
Vol 22 (4) ◽  
pp. 435-438
Author(s):  
M. Vaněčková ◽  
Z. Seidl ◽  
B. Goldova ◽  
I. Vitkova ◽  
A. Baxova ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Case Report ◽  
Magnetic Resonance ◽  
Vascular Malformation ◽  
Renal Agenesis ◽  
Diagnostic Methods ◽  
Post Mortem ◽  
Prenatal Ultrasonography ◽  
Resonance Imaging ◽  
Cerebral Parenchyma

This case report describes a finding of vascular malformation of an aborted foetus of gestational age of the 22nd week. This concerns meningocerebral angiodysplasia, located in the posterior fossa and around the thalami. This disease is rare and is often accompanied by renal agenesis. The finding was complicated by hydrocephalus. Our report compares all three diagnostic methods (prenatal ultrasonography, post-mortem MR and autopsy). Prenatal ultrasonography described only hydrocephalus and reduction of cerebral parenchyma. MR displayed the extent of the malformation, the exact diagnosis was however determined by histological examination. MR described agenesis of structures of midbrain, which was confirmed by autopsy.

Computed tomography and magnetic resonance imaging findings of primary bladder angiosarcoma: a case report

2014 ◽  
Vol 38 (2) ◽  
pp. 212-214 ◽  
Author(s):  
Mehmet Beyazal ◽  
Necip Pirinççi ◽  
Alpaslan Yavuz ◽  
Sercan Özkaçmaz ◽  
Gülay Bulut
Keyword(s):  
Magnetic Resonance Imaging ◽  
Computed Tomography ◽  
Case Report ◽  
Magnetic Resonance ◽  
Imaging Findings ◽  
Resonance Imaging ◽  
Primary Bladder

scholarly journals Lymphangiography and focal pleurodesis treatment of chylothorax with an aberrant thoracic duct following oesophagectomy: a case report

2019 ◽  
Vol 5 (1) ◽  
Author(s):  
Tomoyuki Ishida ◽  
Jun Kanamori ◽  
Hiroyuki Daiko
Keyword(s):  
Magnetic Resonance Imaging ◽  
Interventional Radiology ◽  
Case Report ◽  
Magnetic Resonance ◽  
Thoracic Duct ◽  
Rare Case ◽  
Resonance Imaging ◽  
Case Presentation ◽  
Thoracostomy Tube ◽  
Magnetic Resonance Imaging Mri

Abstract Background Management of postoperative chylothorax usually consists of nutritional regimens, pharmacological therapies such as octreotide, and surgical therapies such as ligation of thoracic duct, but a clear consensus is yet to be reached. Further, the variation of the thoracic duct makes chylothorax difficult to treat. This report describes a rare case of chylothorax with an aberrant thoracic duct that was successfully treated using focal pleurodesis through interventional radiology (IVR). Case presentation The patient was a 52-year-old man with chylothorax after a thoracoscopic oesophagectomy for oesophageal cancer. With conventional therapy, such as thoracostomy tube, octreotide or fibrogammin, a decrease in the amount of chyle was not achieved. Therefore, we performed lymphangiography and pleurodesis through IVR. The patient appeared to have an aberrant thoracic duct, as revealed by magnetic resonance imaging (MRI); however, after focal pleurodesis, the leak of chyle was diminished, and the patient was discharged 66 days after admission. Conclusions Chylothorax remains a difficult complication. Focal pleurodesis through IVR can be one of the options to treat chylothorax.

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