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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. Imaging revealed a pelvic mass and subsequent surgery identified a cystic lesion arising from the uterine fundus. Histopathological examination confirmed a benign MC. This case underscores the importance of considering a broad differential diagnosis for pelvic cystic lesions, especially in patients with a history of mucinous tumors. It highlights the potential diagnostic challenge posed by such a rare presentation and emphasizes the need for further research into mechanisms underlying extra-ovarian recurrences.
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http://dx.doi.org/10.7759/cureus.89387 | 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 PDFJ Psychiatr Brain Sci
June 2025
Department of Psychiatry, School of Medicine, University of Utah, Salt Lake City, UT 84108, USA.
Anxiety disorders are among the most prevalent and debilitating mental illnesses worldwide. While environmental factors such as early-life stress contribute to their etiology, genetics also plays a crucial role, with a family history increasing susceptibility. Unlike Mendelian traits driven by single gene variants, anxiety disorders appear to follow polygenic inheritance in which multiple genetic variants collectively shape risk.
View Article and Find Full Text PDFNeoreviews
July 2025
Division of Neonatology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
Double outlet right ventricle (DORV) is a complex congenital heart disease with a wide spectrum of anatomical variations and clinical presentations. In this conotruncal anomaly, greater than 50% of the semilunar valve diameter of both the aorta and pulmonary artery arises from the morphologic right ventricle. Additionally, patients with DORV have a ventricular septal defect that allows blood to egress from the left ventricle and may obstruct either the pulmonary or systemic circulations.
View Article and Find Full Text PDFBMJ Case Rep
June 2025
Amrita Institute of Medical Sciences and Research Centre, Kochi, KL, India.
Vulvar lichen sclerosus is a chronic, progressive inflammatory dermatosis that predominantly affects postmenopausal women but can also present in premenopausal individuals. It can cause significant scarring, leading to anatomical distortion, urinary dysfunction and impaired quality of life. The author describes a case of a woman in her late 30s with extensive vulvar involvement of lichen sclerosus, resulting in introital stenosis, dyspareunia and painful micturition.
View Article and Find Full Text PDFEndocrine
September 2025
Department of Endocrinology and Metabolism, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Purpose: While primary aldosteronism (PA) is typically screened in hypertensive patients, normotensive PA remains underrecognized, especially in complex cases where standard diagnostic approaches fail. We present a challenging case of normotensive PA complicated by myasthenia gravis (MG) requiring chronic glucocorticoids, which interfere with conventional cortisol-based adrenal venous sampling (AVS) interpretation. This case highlights the pivotal role of Ga-pentixafor PET/CT as an innovative alternative for subtype differentiation in such complex scenarios.
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