An infected urachal cyst forming an abscess: A case report.
Case report
Congenital
Embriological remnant
Urachal cyst
Journal
Radiology case reports
ISSN: 1930-0433
Titre abrégé: Radiol Case Rep
Pays: Netherlands
ID NLM: 101467888
Informations de publication
Date de publication:
Dec 2024
Dec 2024
Historique:
received:
04
08
2024
revised:
18
08
2024
accepted:
19
08
2024
medline:
27
9
2024
pubmed:
27
9
2024
entrez:
27
9
2024
Statut:
epublish
Résumé
Urachal cysts are conditions present at birth that usually occur in children. This disease is very rare in adults. Approximately 35% of patients present with complaints of lower abdominal pain, signs of urinary tract infection, painful lumps in the abdomen, and hematuria. Here we present a case of A 27 year old woman came to the emergency unit with a lump in her stomach since 3 months before admitted to the hospital, located in the lower abdomen, the initial lump was the size of a marble, it got bigger over time and the patient felt feverish. The lump size was the size of a fist and burst open releasing pus and blood. This patient was diagnosed using CT-scan and Ultrasonography. This patient did not undergo any treatment, and chose to go home resulting in a loss to follow up. Urachal residual disease is a rare and manifests with nonspecific abdominal or urinary tract signs and symptoms. Although rare, disorders of the urachus can take the form of acute, life-threatening infections or malignant degeneration. It is important to carry out an accurate diagnosis and appropriate treatment. Urachal anomalies are rare in adults and often undiagnosed due to their nonspecific clinical course. Early diagnosis using several modalities such as ultrasonography and CT-Scan can help in planning an appropriate surgical intervention, thereby reducing morbidity.
Identifiants
pubmed: 39328943
doi: 10.1016/j.radcr.2024.08.103
pii: S1930-0433(24)00883-5
pmc: PMC11424908
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Pagination
5926-5931Informations de copyright
© 2024 The Authors.