Results 41 to 50 of about 6,608 (183)

Robotic-assisted surgery for bilateral synchronous ovarian teratoma and cystadenoma: A case report

Journal of Pediatric Surgery Case Reports, 2020
Reports of different synchronous tumors involving both ovaries are rare, and most fall in the malignant category. This is the case of a 15-year-old female with an unremarkable past medical history who presented with acute onset lower abdominal pain ...
Andrew Peverini, Laura Goodman, Laura Denham, Andrei Radulescu   +3 more
doaj   +1 more source

Rapidly Growing Mucinous Cystadenoma in a 13‐Year‐Old Premenarchal Female: A Case Report

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Mucinous cystadenomas are rare ovarian tumors in premenarchal girls but can present as rapidly growing large abdominal masses causing obstructive symptoms. Early recognition and timely surgical intervention, often requiring salpingo‐oophorectomy, are crucial to prevent complications.
Zeina Marzouk, Ayham Maidaa, Mohammad Obada Alsadi, Rabwa Ibrahim, Basil Daradkeh, Haneen Hussin, Khaledah Aladwan, Husam Dalati   +7 more
wiley   +1 more source

Computed Tomography Angiography‐Assisted Ovarian Vein Sampling for Diagnosing an Androgen‐Producing Leydig Cell Tumor: A Case Report

Case Reports in Endocrinology, Volume 2026, Issue 1, 2026.
Background Ovarian Leydig cell tumors, rare androgen‐producing neoplasms, may present with rapidly progressive virilization. Preoperative localization is frequently challenging, particularly when bilateral ovarian abnormalities coexist or radiologic findings are equivocal.
Ken Tomotsune, Daisuke Saito, Satoshi Saitou, Yusuke Seki, Souta Hayashi, Yumiko Yamashita, Maiko Takata, Kentarou Ohara, Yohei Masugi, Yutaka Saito, Koki Kato, Tomotoshi Hosokawa, Osamu Isozaki   +12 more
wiley   +1 more source

Melanosis tubae et ovarii: An overlooked entity?

Indian Journal of Pathology and Microbiology, 2022
Melanosis is a rare benign entity defined by the deposition of brownish-black pigment in a wide variety of organs especially the gastrointestinal tract, peritoneum, fallopian tubes and ovaries.
Ashutosh Rath, Bhagyashree Priyadarshini, Varuna Mallya, Nita Khurana, Anjali Tempe   +4 more
doaj   +1 more source

Pulmonary Involvement in Proteus Syndrome: Clinical and Imaging Correlates in a Rare Case

Case Reports in Radiology, Volume 2026, Issue 1, 2026.
Proteus syndrome is an uncommon, sporadic disorder characterized by progressive and heterogeneous overgrowth of tissues, resulting in distorted and asymmetric development. In most individuals, Proteus syndrome has minimal to no manifestations at birth but progresses during childhood and adolescence.
Cody Reid Johnson, Syed Muhammad Awais Bukhari, Amit Gupta, Atsushi Komemushi   +3 more
wiley   +1 more source

High‐throughput exosomes analysis for ovarian cancer screening based on a double‐positive surface marker detection biochip

BMEMat, Volume 3, Issue 4, December 2025.
A double‐positive surface marker detection approach was developed to conduct exosome surface protein detection in serum samples. It reaches single‐exosome detection, and over 300 exosome protein parameters are analyzed. The diagnostic accuracy achieved 90% in differentiation of high‐grade serous/serous ovarian carcinoma patients, benign patients, and ...
Jiaoyan Qiu, Yu Wu, Yihe Wang, Chao Wang, Soo‐Yeon Cho, Hui Huang, Yu Zhang, Lin Han   +7 more
wiley   +1 more source

Hepatoid Carcinoma of the Ovary: Case Report, Clinical Management, and Insights From Literature Review

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Hepatoid carcinoma of the ovary (HCO) is an exceedingly rare epithelial ovarian malignancy demonstrating hepatocellular differentiation and marked serum AFP elevation. Due to its rarity, existing literature remains limited, and optimal management strategies remain undefined. Emerging evidence highlights the urgent need for improved recognition
Nan Zhang, Zhilan Liu, Dengfeng Cao, Weihua Lou   +3 more
wiley   +1 more source

Clinical Presentation, Treatment, and Outcomes of 28 Patients With Castleman Disease: A Retrospective Analysis of an Italian Cohort

eJHaem, Volume 6, Issue 6, December 2025.
ABSTRACT Background Castleman disease (CD) encompasses a range of heterogeneous non‐clonal lymphoproliferative disorders, including unicentric (UCD), and multicentric (MCD) forms. The latter is subdivided into HHV‐8+ MCD, POEMS‐MCD, and idiopathic‐MCD, not otherwise specified (iMCD‐NOS).
Caterina Cristinelli, Michele Merli, Marco Lucioni, Manuel Gotti, Roberta Sciarra, Sara Rattotti, Federico Carpi, Gianmarco Favrin, Benedetta Bianchi, Giuseppe Neri, Marta Coscia, Marcello Gambacorta, Francesco Passamonti, Marco Paulli, Luca Arcaini   +14 more
wiley   +1 more source

Study the Expression of Dickkopf-related Protein 3 Immunoreactivity in Serous Epithelial Ovarian Tumors

Medical Journal of Babylon
Background: Dickkopf-related protein 3 (DKK3) is regarded as a tumor suppressor in cancer tissue. DKK3 gene effect has an important role in the prognosis of ovarian cancer with the possibility to discover new line treatment in ovarian cancer.
Ammar Eesa Mahdi, Ali Zaki Naji
doaj   +1 more source

Advances in the Diagnosis, Treatment, and Management of Liver Nodules: A Comprehensive Review

Portal Hypertension &Cirrhosis, Volume 4, Issue 4, Page 232-251, December 2025.
Liver nodules commonly occur due to various causes, some of which are malignant or may undergo malignant transformation, leading to disease progression or delayed detection in clinical practice. The widespread use of imaging methods has increased the detection rate of liver nodules. Furthermore, precision medicine techniques and artificial intelligence
Chang Gao, Dongyang Chen, Youpeng Chen
wiley   +1 more source