Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
Laparoscopic peritoneal mucinous cystadenoma debulking: A case report.
Medicine (Baltimore)
January 2025
Department of General Surgery, Nujiang Prefecture People's Hospital, Yunnan, Nujiang, China.
Rationale: Peritoneal mucinous cystadenoma is rare in the clinic, lacks specific clinical manifestations, tumor markers, and imaging features, and is easily misdiagnosed and missed. Clinical practitioners should maintain a high level of vigilance. Here, we report a case of laparoscopic peritoneal mucinous cystadenoma stripping to improve our understanding of the disease.
View Article and Find Full Text PDFIntrahepatic Class VII Choledochal Cyst: Radiological Insights and Surgical Approach.
Am J Case Rep
December 2024
Department of Surgery, Faculty of Medicine, Al-Baha University, Al-Baha, Saudi Arabia.
Article Synopsis
- Choledochal cysts are congenital bile duct abnormalities classified into five main types, with this case focusing on an intrahepatic variant mistaken for biliary cystadenoma.
- A 35-year-old woman experienced pain and a palpable mass, leading to diagnostic imaging that revealed a complicated cyst affecting her liver's bile ducts.
- Surgical intervention was required due to the cyst's complexity, and while the gallbladder was removed, the cyst could not be entirely separated from the common hepatic duct, highlighting the need for careful evaluation to prevent complications.
Undifferentiated embryonal sarcoma of the liver masquerading as a cystadenoma in a young adult: a case report.
J Med Case Rep
November 2024
Department of Radiology, Affiliated Hangzhou First People's Hospital, Westlake University School of Medicine, Hangzhou, 310006, China.
Article Synopsis
- Undifferentiated embryonal sarcoma of the liver is a rare cancer mostly affecting children, and is even less common in adults; proper imaging is crucial to avoid misdiagnosing it with more common liver masses.
- A 37-year-old Chinese woman presented with abdominal pain and underwent multiple imaging tests revealing a cystic-solid liver nodule, initially thought to be benign.
- The definitive indication of malignancy came from a PET-CT scan, which showed abnormal F-fluorodeoxyglucose uptake, prompting the correct diagnosis of undifferentiated embryonal sarcoma of the liver.
Mucinous cystadenoma of the caecum: a rare cause of recurrent intussusception in a 3-year-old boy (case report).
Pan Afr Med J
October 2024
Department of Surgery, Korle-Bu Teaching Hospital, Accra, Ghana.
Mucinous cystadenoma of the caecum is an exceptionally rare occurrence, particularly in paediatric patients. They have been rarely reported in the appendix, ovary, pancreas, and liver. This is the first report of a mucinous cystadenoma of the caecum (to the best of the authors' knowledge) in a child.
View Article and Find Full Text PDFCT, MRI and contrast-enhanced ultrasound features of mucinous cystic neoplasm of the liver.
Diagn Interv Imaging
October 2024
Department of Radiology, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, 75014, Paris, France; Université Paris Cité, Faculté de Médecine, 75006 Paris, France.
Want 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!