We report what to our knowledge is the first case of a giant multicystic cystadenoma of the Cowper's glands. An otherwise healthy 41-year-old man presented with acute urinary retention. Physical examination showed a perineal mass. Different imaging techniques demonstrated a multicystic tumor and en bloc excision was performed. Histological evaluation showed that the tumor arised from the bulbourethral glands; immunohistochemistry proved positive staining for high molecular weight cytokeratin. CASE HYPOTHESIS: Cystic tumors in the pelvis can arise from different structures. Malignancy should be ruled out. Surgical excision can be diagnostic and curative. Future implications: When evaluating a pelvic cystic tumor, Cowper's glands cystadenoma may be a differential diagnosis and must be considered. Similar to prostate cystadenomas, en bloc excision is the optimal treatment.
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http://dx.doi.org/10.1590/S1677-5538.IBJU.2013.05.17 | DOI Listing |
Radiol Case Rep
November 2024
Urology Department, CHU Marie Curie, Charleroi, Belgium.
Seminal vesicle cystadenomas (SVC) are exceedingly rare benign tumors, with only 22 cases reported in the literature up to 2018. Here, we present the case of a 40-year-old man who presented with acute urinary retention secondary to a giant pelvic mass. Radiological imaging diagnosed a retrovesical well-delimited multicystic tumor, initially suspected to arise from the left lobe of the prostate but ultimately confirmed to originate from left seminal vesicle.
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July 2024
Gastroenterology and Hepatology, St. Luke's Hospital, Chesterfield, USA.
Autoimmune pancreatitis (AIP) is acknowledged as a benign ailment with swift responsivity to corticosteroid treatment (CST). Though past assumptions dismissed its connection to cyst formation, a few instances of AIP-linked pancreatic cysts (PCs) have been documented. While some cases responded positively to CST, others demonstrated resistance, necessitating intervention.
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April 2024
Radiodiagnosis, Dr D.Y. Patil Medical College, Hospital and Research Centre, Pune, IND.
A 19-year-old girl with a short stature and presenting low intelligence quotient, illegible speech, and a greatly distended abdomen was seen at the gynecological outpatient department. She underwent investigation and was found to have large abdominopelvic multicystic ovaries with no malignant features and CA125 levels within the normal range for premenopausal women. Her thyroid-stimulating hormone (TSH) was markedly elevated.
View Article and Find Full Text PDFActa Chir Belg
June 2024
Medico-Surgical Department of Gastroenterology, Hepatopancreatology and Digestive Oncology, Hôpital Universitaire de Bruxelles (HUB), Belgium.
Background: Multicystic mesothelial cyst is a rare, and usually benign, tumor which is rarely diagnosed preoperatively due to the poor specificity of its symptomatology.
Methods: We report the case of a 63-year-old man with multiple comorbidities (e.g.
Children (Basel)
May 2023
Faculty of Medicine and Pharmacy, "Dunărea de Jos" University, 800216 Galați, Romania.
Struma ovarii (SO) is a monodermal teratoma containing at least 50% thyroid tissue. Classically, SO is a hormonally inactive benign neoplasm that occurs in premenopausal women, and has unspecific clinical and imaging features. Its treatment is surgical and its diagnosis is established histopathologically.
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