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http://dx.doi.org/10.3949/ccjm.88a.20132 | DOI Listing |
Diagnostics (Basel)
August 2025
New England Trophoblastic Disease Center, Division of Gynecologic Oncology, Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Hydatidiform mole is a trophoblastic disorder resulting from abnormal fertilization. Diagnosis is established through a combination of clinical findings, elevated serum human chorionic gonadotropin (hCG) levels, and characteristic features on transvaginal ultrasound. Timely and accurate diagnosis is essential for initiating prompt treatment and preventing medical complications.
View Article and Find Full Text PDFCent European J Urol
May 2025
Department of Urology, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom.
Introduction: Aim of the study was to evaluate and illustratively depict the aspiration properties of a single-use 7.5 Fr flexible ureteroscope with direct-in-scope suction (DISS) in a specifically designed setting.
Material And Methods: An experimental study using a 6.
J Nippon Med Sch
August 2025
Department of Gastroenterological Surgery, Nippon Medical School.
Mucinous cystic neoplasms of the liver (MCNs-L) are rare cystic tumors characterized by multilocular cysts lined with a mucin-producing epithelium and supported by ovarian-like stroma. These tumors account for <5% of all cystic liver lesions and carry a potential risk of malignant transformation, necessitating early diagnosis and surgical resection. This report describes the successful laparoscopic partial liver resection of segments 4 and 5 for a large MCN-L in a woman in her 40s who presented with upper abdominal discomfort.
View Article and Find Full Text PDFCurr Oncol
July 2025
Thoracic Surgery Department, "Theageneio" Cancer Hospital, 54639 Thessaloniki, Greece.
Malignant mediastinal tumors are a group representing some of the most demanding oncological challenges for early, multi-level, and successful management. The timely identification of any suspicious clinical symptomatology is urgent in achieving an accurate, staged histological diagnosis, in order to follow up with an equally detailed medical therapeutic plan (interventional or not) and determine the principal goals regarding efficient overall treatment in these patients. We report a case of a 24-year-old male patient with an incident-free prior medical history.
View Article and Find Full Text PDFWorld J Gastrointest Oncol
August 2025
Department of Hematology, Affiliated Hospital of Nantong University, Nantong 226001, Jiangsu Province, China.
Background: Thrombotic microangiopathy (TMA) is an acute syndrome characterized by microangiopathic hemolytic anemia, thrombocytopenia, and multi-organ dysfunction due to the microcirculation of platelet thrombi. Cancer-associated TMA is a rare and fatal complication, which often occurs during cancer remission. It is frequently misdiagnosed because of limited clinical awareness.
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