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Testicular mucinous cystadenoma is a rare benign testicular tumor with the characteristics of being potentially malignant and showing atypical clinical symptoms; this article reports a case of a primary testicular mucinous cystadenoma misdiagnosed as testicular teratoma by ultrasound. A 69-year-old man was admitted to the hospital because of a 1-year history of left-sided testicular enlargement with scrotal swelling and no obvious abnormalities on laboratory tests. Ultrasound examination revealed solid-mass lesions in the left testicle, suggesting a high probability of teratoma, and contrast-enhanced magnetic resonance imaging (MRI) examination suggested an increased possibility of epidermoid cysts. Contrast-enhanced computed tomography (CT) and contrast-enhanced MRI of the preoperative abdomen and pelvis showed no other primary adenocarcinoma. Doctors performed radical resection of the left testicle. The postoperative pathological diagnosis was mucinous cystadenoma, and calcification as well as partially mildly atypical epithelial cells were discovered. Furthermore, there were no neoplastic lesions in the epididymis or spermatic cord. No metastatic lesions were found after 6 months postoperative follow-up, and the patient's prognosis remains good.
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http://dx.doi.org/10.3389/fonc.2023.1206697 | DOI Listing |
Cureus
August 2025
Department of Surgical Oncology, CION Cancer Clinics, Hyderabad, IND.
Extra-ovarian recurrence of mucinous cystadenomas (MCs) is a rare phenomenon. This case report presents the first documented instance of a benign MC recurring within the uterine myometrium of a 48-year-old woman. Two years following an oophorectomy for a large left ovarian MC, the patient presented with lower abdominal pain.
View Article and Find Full Text PDFWorld J Clin Oncol
August 2025
General Surgery Unit I - Liver Service, Fondazione IRCCS Policlinico San Matteo, Pavia 27100, Italy.
Mucinous cystic neoplasms of the liver (MCN-L) are rare cystic lesions characterized by mucin-producing epithelium and ovarian-like stroma. Although they constitute fewer than 5% of hepatic cystic lesions, MCN-L poses significant diagnostic challenges due to overlapping features with other cystic lesions and their potential for malignant transformation. Early recognition and definitive surgical intervention are therefore critical to ensure optimal patient outcomes.
View Article and Find Full Text PDFExp Ther Med
October 2025
Department of Gastroenterology, Xixi Hospital, Hangzhou, Zhejiang 310023, P.R. China.
Hepatic mucinous cystic neoplasms (MCN) are rare cystic tumors that are predominantly observed in females, with a low incidence rate in males. To date, few cases of aggressive MCN have been reported in male patients. The current study reports the case of a 74-year-old male patient who presented to Xixi Hospital with abdominal distension.
View Article and Find Full Text PDFForensic Sci Med Pathol
August 2025
Department of Forensic Medicine, Wakayama Medical University, 811-1 Kimiidera, Wakayama, 641-8509, Japan.
We herein report a case of sudden death from massive mucinous cystadenoma of the ovary. A female in her 70s was found dead with an enlarged abdomen. Forensic autopsy was performed to identify the cause of death.
View Article and Find Full Text PDFJ Reprod Infertil
January 2025
Barnsley Hospital NHS Foundation Trust, Obstetrics and Gynaecology Department, Barnsley Hospital, South Yorkshire, UK.
Background: The recurrence of benign ovarian mucinous cystadenomas is rare, and the presence of these cysts bilaterally is even more uncommon. Overall, 11 cases in our literature review were identified. Of these recurrences, only two cases were bilateral.
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