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| http://dx.doi.org/10.1007/s13224-015-0694-9 | DOI Listing |
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Urachal adenocarcinoma in an adolescent girl: A case report.
Int J Surg Case Rep
January 2025
Department of Surgery, Aga Khan Hospital, P.O. Box 2289, Dar Es Salaam, Tanzania; Department of Surgery, Aga Khan University, P.O. Box 38129, Dar Es Salaam, Tanzania.
Introduction: The urachus is a fetal canal that connects the allantois to the bladder and typically obliterates by the 6th month of gestation. Failure of the urachus to obliterate can result in urachal anomalies, which, in rare cases, may undergo malignant transformation.
Case Presentation: We present a case of a 13-year-old female who experienced hematuria, dysuria, and abdominal pain persisting for over 4 months.
Spontaneous Hepatic Rupture Complicating Preeclampsia and HELLP Syndrome: A Case Report.
Case Rep Med
December 2024
Department of Surgery, Jimma Medical Center, Jimma University, Jimma, Ethiopia.
Spontaneous hepatic rupture is a rare complication that occurs in pregnant mothers with HELLP syndrome, or preeclampsia with severe features, or eclampsia. The most common symptom of hepatic rupture/hematoma is right upper quadrant pain or epigastric pain, which is similar to the presentation of preeclampsia with severe features. Therefore, the absence of specific signs and symptoms leads to a diagnostic dilemma and a delay in management.
View Article and Find Full Text PDFUterine rupture with induction using misoprostol for intrauterine foetal death in the second trimester: A case report.
Case Rep Womens Health
December 2024
Médecins Sans Frontières-Belgique (OCB), Avenue 7 Février, Grande passe, Port-à-Piment, Haïti.
Uterine rupture is a well-known, life-threatening complication of misoprostol use; the incidence is remarkably low. Herein, we report what seems to be the first documented case of uterine rupture following induction of labour for intrauterine foetal death in the second trimester without a uterine scar. A 40-year-old woman with no history of caesarean section or uterine surgery presented with mild lower abdominal pain and mild genital bleeding.
View Article and Find Full Text PDFSurgical management of a massive omphalocele in a newborn: A case report study.
Int J Surg Case Rep
November 2024
Department of Nursing, School of Nursing and Midwifery, Islamic Azad University - Tabriz Branch, Tabriz, Iran.
Article Synopsis
- - Omphalocele is a rare congenital defect, affecting 1 in 5,000 to 10,000 newborns, where abdominal organs push through a gap at the base of the umbilical cord, requiring complex surgical treatment to prevent serious complications.
- - A case study illustrates a female newborn with a large omphalocele who underwent an urgent cesarean delivery; a staged surgical approach was used, involving a silo for organ reduction and closure with absorbable sutures and biologic mesh.
- - The case emphasizes the importance of coordinated care among pediatric surgeons and personalized treatment plans, as the patient is now thriving six months post-surgery with no complications.
Fetus in the Abdominal Cavity After Uterine Rupture in a Primigravida Post-Adenomyosis Enucleation.
Diagnostics (Basel)
November 2024
Department of Obstetrics and Gynecology, Nihon University School of Medicine, Tokyo 173-8610, Japan.
A 35-year-old primigravida with a history of adenomyosis enucleation was diagnosed with abnormal fetal position at 25 weeks of gestation. The patient presented with normal vital signs and no symptoms. A cardiotocogram and transabdominal ultrasound revealed a healthy fetus, normal amniotic fluid volume, and no intra-abdominal bleeding.
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