Results 91 to 100 of about 1,779 (161)
From classroom to clinic: Evaluating the educational utility of two Thiel embalming methods
Anatomical Sciences Education, Volume 19, Issue 10, Page 1682-1696, October 2026.Abstract Over three decades since its introduction, the Thiel embalming method remains a widely used and praised technique in anatomical education and clinical training. This study compared for the first time the Thiel original protocol (TO) and a Modified version (TM) across user groups—undergraduate medical students, student demonstrators in anatomy,
Veronica Antipova +3 more
wiley +1 more source
CDS2 Drives Tumor Progression in Epithelial Ovarian Cancer via the PI3K/AKT Pathway
Cancer Medicine, Volume 15, Issue 10, October 2026.ABSTRACT Background Epithelial ovarian cancer (EOC) frequently disseminates within the lipid‐rich peritoneal cavity, where tumor progression is accompanied by metabolic adaptations involving lipid utilization and mitochondrial function. Although these metabolic alterations are increasingly recognized as important features of EOC progression and ...
Lixue Cao +10 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 10, October 2026.ABSTRACT Although rare, ruptured mature cystic teratoma (MCT) can cause chronic granulomatous peritonitis that mimics peritoneal carcinomatosis. In patients with a history of cystectomy for MCT, careful clinicoradiologic and histopathologic correlation is essential to avoid misdiagnosis and unnecessary aggressive treatment.
Zohre Sadeghian +6 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 10, October 2026.ABSTRACT In a patient with advanced ovarian cancer showing limited response to paclitaxel–carboplatin, adding sintilimab was associated with R0 cytoreduction and sustained disease‐free status during olaparib–bevacizumab maintenance. This case provides a rationale for further investigation of PD‐1 blockade as neoadjuvant therapy in carefully selected ...
Wang Zhenyan, Wang Yan
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 10, October 2026.ABSTRACT Cervical carcinosarcoma (CCS), also known as malignant mixed Müllerian tumor (MMMT) of the cervix, is an exceptionally rare and aggressive biphasic neoplasm composed of both epithelial and mesenchymal malignant components. Due to its rarity, optimal management strategies are not well established, particularly in low‐resource settings.
John Lugata +11 more
wiley +1 more source
Umbilical Hernia in a Ram and Its Successful Surgical Repair
Clinical Case Reports, Volume 14, Issue 10, October 2026.Description: Clinical presentation showing a distinct umbilical swelling (A). Prepared surgical site after clipping and aseptic scrubbing (B). Draped surgical field, secured with towel clamps (C). Extension of the stab incision hernia sac under digital guidance (D). Hernial ring after reduction of the herniated contents (E). Closure of the hernial ring
Getachew Tadesse Siyoum
wiley +1 more source
Pyloric Pseudonecrosis Caused by Biliary Peritonitis: A Rare Intraoperative Pitfall
Clinical Case Reports, Volume 14, Issue 10, October 2026.ABSTRACT Biliary peritonitis can cause subserosal bile staining that mimics pyloric or duodenal necrosis. When endoscopy or ICG fluorescence is unavailable, pseudonecrosis remains an operative diagnosis of exclusion, supported by preserved serosal integrity, absence of visible perforation, careful inspection, and uneventful 1‐month follow‐up.
Christian Mouawad +2 more
wiley +1 more source
A Case Report of Cecal Perforation Due to Sigmoid Tumor Incarceration in Inguinal Hernia
Clinical Case Reports, Volume 14, Issue 10, October 2026.ABSTRACT This case highlights an unusual presentation in which incarceration of a sigmoid tumor within an inguinal hernia sac resulted in colonic obstruction and subsequent cecal perforation, emphasizing the importance of prompt imaging and surgical evaluation in patients with this rare combination.
Mojtaba Ahmadinejad +4 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 10, October 2026.ABSTRACT Sertoli–Leydig cell tumors (SLCTs) are rare ovarian sex cord‐stromal tumors, particularly uncommon in the pediatric population. They are typically androgen‐secreting, while estrogen‐secreting forms are rare and may lead to diagnostic confusion with granulosa cell tumors.
Sanaa Bouramdane +7 more
wiley +1 more source