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Preoperative magnetic resonance evaluation of Struma Ovarii and its importance for the surgical modality: a retrospective study from two institutions.
Abdom Radiol (NY)
January 2025
Department of Radiology, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, China.
Objectives: To improve preoperative diagnostic accuracy of struma ovarii by retrospectively reviewing magnetic resonance (MR) findings. It is beneficial to choose the most appropriate surgical modality for the patient.
Methods: We retrospectively reviewed the clinical course and MR characteristics of 52 patients who were diagnosed postoperatively with struma ovarii, pathologically, from two institutions.
Orbital Lymphangioma in an Adolescent Male: A Case Report and Review of Literature.
Cureus
November 2024
Radiodiagnosis, MNR Medical College and Hospital, Sangareddy, IND.
Lymphangiomas are localized multi-cystic malformations of the lymphatic and vascular system, primarily affecting the head and neck regions in children. Orbital lymphangiomas are not considered hamartomas because the orbit does not commonly display lymphatic vessels. In this case report, we describe a male patient who was 15 years old and presented to our medical facility with the primary complaints of having a bulging left eye, sudden chemosis of the lower conjunctiva, and pain in the left eye.
View Article and Find Full Text PDFAssessing masked hypertension and ambulatory arterial stiffness index in children congenital kidney malformations.
Clin Exp Nephrol
December 2024
Department of Pediatric Nephrology, Ulus Maternity and Child Health and Diseases Training and Research Hospital, Dr. Sami, Ankara, Turkey.
Background: Patients diagnosed with congenital kidney malformations are at an increased risk of developing hypertension, proteinuria, and progressing to chronic kidney disease (CKD). The present study aimed to determine the frequency of masked hypertension and ambulatory arterial stiffness index (AASI) in patients with congenital kidney malformations.
Methods: The study included 174 patients with congenital kidney malformations (48 patients with unilateral renal agenesis (URA), 40 patients with ectopic kidney (EK), 36 patients with horseshoe kidney (HK), 31 patients with multicystic dysplastic kidney (MCDK), 19 patients with unilateral renal hypoplasia (URH), and 45 healthy controls.
Prenatal diagnosis, ultrasound findings, and pregnancy outcome of 17q12 deletion and duplication syndromes: a retrospective case series.
Arch Gynecol Obstet
December 2024
Department of Community Center, Longgang District People's Hospital of Shenzhen City (The Second Affiliated Hospital of The Chinese University of Hong Kong, Shenzhen), Shenzhen, Guangdong, China.
Article Synopsis
- - The study examined ultrasound findings and SNP-array results for fetuses with 17q12 deletions and duplications during the second and third trimesters, focusing on prenatal characteristics and outcomes.
- - Data from 16 fetuses with deletions and 7 with duplications were analyzed, revealing significant abnormalities; deletions often led to renal issues, while duplications were associated with cardiovascular and gastrointestinal problems.
- - Out of the pregnancies, 9 were terminated, while 14 continued; some cases presented multiple severe structural malformations, highlighting the complexity of conditions associated with these genetic variations.
Supporting Infants with Multicystic Dysplastic Kidney Disease: A Comprehensive Approach.
Neonatal Netw
October 2024
Multicystic dysplastic kidney (MCDK) is a congenital renal disease characterized by variable-sized noncommunicative cysts, impeding parenchymal development and functionality. Renal capabilities are relative to the functionality of the contralateral kidney and response to management. Unilateral and isolated cases are often asymptomatic with more positive outcomes, while severe bilateral derangements have a high mortality rate.
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