Giant multilocular prostatic cystadenomas are rare benign prostatic tumor, usually presenting as a large pelvic mass, compressing the adjacent organs but with no clear aggressive features, frequently causing obstructive voiding symptoms. Nowadays, imaging plays an important role on the adequate characterization of these lesions, not only on depicting their different internal components, but also the relationship with the adjacent structures, therefore providing the best preoperative surgical planning. Here we present a case of a 62-year-old patient with recurrent obstructive voiding symptoms due to a giant multilocular prostatic cystadenomas, with histologically correlation, posteriorly excised.
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796614 | PMC |
| http://dx.doi.org/10.1016/j.radcr.2019.09.017 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
A giant ovarian atypical proliferative mucinous tumor in a young adult: A rare case report and review of the literature.
Int J Surg Case Rep
January 2025
Faculty of Medicine, Kilimanjaro Christian Medical University College, Moshi, Tanzania; Department of Pathology, Kilimanjaro Christian Medical Centre, Moshi, Tanzania; Kilimanjaro Clinical Research Institute, Moshi, Tanzania. Electronic address:
Introduction And Importance: Ovarian atypical proliferative mucinous tumor (APMT) is a low-malignant or borderline tumor that originates from the ovary's surface epithelium. This tumor can grow to a massive size, causing abdominal distention, which can result in a variety of compression symptoms if it is not discovered early.
Case Presentation: A 23-year-old female presented with a chronic, gradually developing abdominal distention that had been persistent for a year.
Central Giant Cell Tumour of the Maxillofacial Region: A 10-Year Retrospective Analysis.
J Maxillofac Oral Surg
December 2024
Oral and Maxillofacial Surgery, MDC Delhi Cantt, New Delhi, India.
Article Synopsis
- - The study analyzed 157 cases of central giant cell tumour (CGCT) in the jaws over ten years, focusing on demographic data, treatment methods, and complications.
- - It found a higher prevalence in females (87) compared to males (70), with most cases located in the maxilla (62%) and presenting symptoms like facial asymmetry and paraesthesia.
- - Various surgical interventions were employed, such as maxillectomy and mandible resections, with low complication rates, highlighting the need for accurate diagnosis and careful treatment planning.
Complete resection of a giant costal chondrosarcoma with reconstruction of the thoraco-abdominal wall: a case report.
J Cardiothorac Surg
November 2024
Department of Thoracic Surgery, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, No. 55, Section 4, South Renmin Road, Chengdu, 610041, Sichuan, China.
Article Synopsis
- Chondrosarcoma most often forms in the pelvis and femur, and while surgical removal is the main treatment for tumors in the ribs, it can create significant challenges for chest wall reconstruction.
- A 49-year-old woman with a diagnosed Grade I chondrosarcoma had a large mass affecting her ribs and diaphragm, leading to a complete surgical resection of the tumor and surrounding affected structures, followed by reconstruction using mesh and sutures.
- The histopathology revealed a Grade II chondrosarcoma, but the patient had an uneventful recovery, highlighting the need for careful planning and collaborative approaches in treating such cases.
Giant cystic lymphangioma as a rare cause of acute abdomen in infancy: a case report and literature review.
Folia Med (Plovdiv)
October 2024
Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece.
Lymphangioma, a benign mass of lymphatic origin, primarily affects the head, neck, and oral cavity, with the abdomen being an uncommon location. Clinical presentation is defined by site of origin and size. We present the case of a 10-month-old male infant with no previous medical history, admitted to our department with diffuse abdominal pain and distension.
View Article and Find Full Text PDFCentral odontogenic fibroma: retrospective study of six cases with variable histopathologic features using 2022 WHO classification.
BMC Oral Health
October 2024
Department of Oral and Maxillofacial Pathology, Faculty of Dentistry, Mahidol University, Yothi Street, Bangkok, 10400, Thailand.
Background: Central odontogenic fibroma (COF) is a rare benign odontogenic tumor with a wide range of histopathologic features. We evaluated COF diagnosed in our institute with 16 years' experience using 2022 WHO classification.
Methods: Our archives were reviewed and cases diagnosed as COF were selected.
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!