While cystic dysplasia of the testis is rare, the awareness of the benign and malformative nature of this lesion is important to consider among other cystic testicular and para testicular lesions, first neoplasm. Its sonographic appearance and the recognition of simultaneously occurring renal anomalies should allow for prompt recognition in children with scrotal swelling or testicular enlargement. We describe a 10-year-old boy with right testicular swelling who underwent orchiectomy for cystic dysplasia of the testis.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1055/s-2008-1071054 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Intraductal Papillary Mucinous Neoplasm of the Bile Duct: A Case Report.
Cureus
February 2025
Gastroenterology and Hepatology, Baylor Scott & White All Saints Medical Center, Fort Worth, USA.
Intraductal papillary mucinous neoplasms (IPMNs) are a prevalent subtype of pancreatic cystic lesions, especially among individuals with liver cirrhosis. Intraductal papillary neoplasms of the bile duct (IPNBs) differ in histopathology based on the location and cellular variability in each location. Intrahepatic IPNBs are less aggressive than the extrahepatic variant, highlighting its heterogeneity and complexity.
View Article and Find Full Text PDFPeriungual Cyst or Pseudocyst Featuring Low-Grade Dysplasia Associated With High-Risk Human Papillomavirus Infection: A Cystic Presentation of Human Papillomavirus-Related Intraepithelial Neoplasia of the Nail Bed?
Am J Dermatopathol
February 2025
Department of Pathology, Hôpital Universitaire de Bruxelles (HUB), Brussels, Belgium.
Mesenchymal dysplasia of the placenta: a rare entity and important differential diagnosis. Presentation of a case with placentomegaly.
Z Geburtshilfe Neonatol
February 2025
MVZ Abts & Partner Mølledam, Flensburg, Germany.
Placental mesenchymal dysplasia (PMD) is a rare disease with unclear etiology and peculiar placental findings (placentomegaly, abnormal chorionic vessels with thromboses, and grossly enlarged and often cystic-appearing stem villi). Songraphic findings are cystic changes, hypoechoic areas, placental enlargement, and dilated chorionic vessels.PMD can be associated with severe perinatal complications, e.
View Article and Find Full Text PDFCiliated hepatic foregut cysts: a large retrospective single-centre series.
Scand J Gastroenterol
February 2025
Department of Clinical Sciences, Karolinska Institutet, Danderyds Hospital, Stockholm, Sweden.
Objective: This study aimed to provide insight about clinical management of ciliated hepatic foregut cysts (CHFC) at a tertiary centre.
Background: CHFC is a rare cystic lesion of the liver with malignant potential according to previous reports. However, the current recommendation to resect all cysts in fit patients is based on limited evidence.
The concept of dysplasia in the lining of odontogenic keratocyst: A case report and review of the literature.
J Oral Maxillofac Pathol
December 2024
Department of Oral Pathology and Microbiology, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, Tamil Nadu, India.
Odontogenic keratocyst (OKC) is an uncommon developmental cyst with a high recurrence rate. Epithelial dysplasia is a rarely recognized phenomenon in OKCs, with only a few acceptable cases reported in the literature. The exact pathogenesis of dysplastic changes in epithelial lining is difficult to explain, in the absence of molecular analyses.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!