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Transurethral unroofing of a Cowper's syringocele.
Urol Case Rep
January 2025
Fox Chase Cancer Center, Department of Urology, Philadelphia, PA, 333, Cottman Ave, Philadelphia, PA, 19111, USA.
Syringoceles are cystic dilations of the bulbourethral gland, also known as Cowper's gland. Syringoceles are a rare pathology with no standard treatment. Herein, we report the diagnosis and endoscopic management of an imperforate syringocele causing bothersome urinary symptoms in an adult male patient.
View Article and Find Full Text PDFA rare case of acute urinary retention due to hematocolpos in a 15-year-old girl: A case report.
Int J Surg Case Rep
January 2025
General Referral Hospital of Musienene, Territory of Lubero, North Kivu, Democratic Republic of the Congo.
Introduction And Importance: Acute urinary retention (AUR) is uncommon in pediatric and adolescent populations, particularly among females. To highlight the presentation of AUR as a symptom of hematocolpos due to an imperforate hymen in a 15-year-old girl.
Case Presentation: A 15-year-old girl presented with AUR and lower abdominal pain, which led to the diagnosis of hematocolpos.
Sirenomelia-Challenges and Treatment Approach in a Rare Case.
Birth Defects Res
December 2024
The Department of Surgery and Urology for Children and Adolescents, Medical University of Gdansk, Gdansk, Poland.
Introduction: Sirenomelia is a very rare congenital structural anomaly characterized by abnormal development of the caudal region of the body with varying degrees of fusion of lower limbs. Mostly, the condition is lethal for the baby. Most babies do not survive even after surgery.
View Article and Find Full Text PDFImperforate nasopharynx in a cat successfully treated with an extended palatoplasty.
JFMS Open Rep
December 2024
Glendale Veterinary Clinic, Glendale, NY, USA.
Case Summary: A female intact domestic shorthair kitten was evaluated at 8 months of age for bilateral mucopurulent nasal discharge, stertor, open-mouth breathing and difficulty eating. Imperforate nasopharynx (INP) was diagnosed on oronasal examination under anesthesia. An extended palatoplasty was performed and resulted in resolution of the clinical signs.
View Article and Find Full Text PDFJohanson-Blizzard syndrome with cystic dilation of the cochlea and hypoplastic modiolus: a case report.
Pediatr Radiol
January 2025
St. John's Medical College Hospital, Sarjapur Road, Koramangala, Karnataka, 560034, Bengaluru, India.
Johanson-Blizzard syndrome is a rare genetic disorder characterised by various systemic manifestations, including sensorineural hearing loss. We present a unique case of a 3.5-year-old girl with genetically confirmed Johanson-Blizzard syndrome, who exhibited typical features alongside rare radiological findings of cystic dilation of the cochlea and hypoplastic modiolus.
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