Results 41 to 50 of about 22,832 (156)

The Uterine Adenosarcoma in a Young Woman Treated by TAH/BOS and Combined Adjuvant Therapy: A Case Report

Acta Medica Iranica, 2020
Objective: We aimed to report a woman suffering from uterine adenosarcoma in perimenopause period Case report. The patient had undergone total abdominal hysterectomy (TAH) with bilateral salpingo-oophorectomy (BSO) and also received adjuvant ...
Soodabeh Shahidsales, Marjaneh Farazestanian, Noorieh Sharifi‐Sistani, Sara Rasta, Seyed Alireza Javadinia   +4 more
doaj   +1 more source

sj-pdf-1-imr-10.1177_03000605221089546 - Supplemental material for The first successful treatment and genetic sequencing of primary hepatic adenosarcoma with sarcomatous overgrowth: a case report

, 2022
Supplemental material, sj-pdf-1-imr-10.1177_03000605221089546 for The first successful treatment and genetic sequencing of primary hepatic adenosarcoma with sarcomatous overgrowth: a case report by Hanjie Hu, Qianqian Song, Hong Zhao, Bo Zheng and ...
Qianqian Song (697197), Hanjie Hu (7317824), Bo Zheng (170888), Haizhen Lu (543209), Hong Zhao (325)   +4 more
core   +1 more source

Immunohistochemical markers and the clinical course of adenosarcoma: a series of seven cases

Diagnostic Pathology, 2020
Background Uterine adenosarcoma, a rare uterine tumor subtype, is a biphasic tumor consisting of epithelial and mesenchymal elements. To date, there is no research comparing the histopathological features and immunohistochemistry of primary and recurrent
Makiko Omi, Akiko Tonooka, Tomohiro Chiba, Yuji Tanaka, Atsushi Fusegi, Yoichi Aoki, Hidetaka Nomura, Hiroyuki Kanao, Yutaka Takazawa   +8 more
doaj   +1 more source

Mullerian adenosarcoma (heterologous) of the cervix with sarcomatous overgrowth: a case report with review of literature. [PDF]

J Gynecol Oncol, 2010
Mullerian adenosarcoma is a rare biphasic malignant neoplasm of the cervix characterized by an admixture of benign epithelial elements and a malignant sarcomatous stromal component, which may be either homologous or heterologous. An aggressive variant of adenosarcoma, mullerian adenosarcoma with sarcomatous overgrowth (MASO) is extremely rare, with ...
Duggal R, Nijhawan R, Aggarwal N, Sikka P.   +3 more
europepmc   +4 more sources

A Single-Centre Experience on the Management of Adenosarcoma: A Successful Report of an Integrated Medical and Surgical Approach

Clinical Medicine Insights: Oncology, 2018
Adenosarcomas are the rarest form of uterine sarcomas, and clinical experience with their management is still limited. Here, we reported 7 patients with uterine adenosarcoma referred to our institution, focusing on main pathologic features, their medical
Margherita Nannini, Giulia Dondi, Donatella Santini, Antonio De Leo, Angelo Paolo Dei Tos, Claudio Zamagni, Maristella Saponara, Lidia Gatto, Concetta Nigro, Paola Bertaccini, Maurizio Zompatori, Pierandrea De Iaco, Anna Myriam Perrone, Maria Abbondanza Pantaleo   +13 more
doaj   +1 more source

Microsatellite Instability Status and the Expression of p16 and Cyclin D1 Proteins in Uterine Adenosarcoma and Their Clinicopathological Significance

Türk Patoloji Dergisi, 2023
Objective: Uterine adenosarcoma has low malignant potential, except in cases with sarcomatous overgrowth (SOG) and a high-grade morphology. We here point out the prognostic clinicopathological and immunohistochemical features as well as the ...
Alev OK ATILGAN, Eda YILMAZ AKCAY, Ozlem OZEN, A. Nihan HABERAL REYHAN, Ali AYHAN   +4 more
doaj   +1 more source

A Rare Case Report on Dedifferentiated Liposarcoma of the Thigh Mimicking an Abscess With Vascular Features: A Diagnostic Challenge With Fatal Outcome

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Dedifferentiated liposarcoma (DDLPS) is an aggressive malignant soft tissue tumor comprising approximately 15%–20% of all liposarcomas. When presenting in the extremities, its atypical clinical and radiological features may mimic vascular or infectious conditions, posing a serious diagnostic challenge that can delay curative intervention. A 60‐
Rashid Shahriar Sazal, Md. Hashibul Hasan Shawon, Mahin Zubaer, Md. Abul Kalam Azad, Khaled Mahbub Murshed, Kazi Ali Aftab   +5 more
wiley   +1 more source

Diffuse‐Type Tenosynovial Giant Cell Tumor of the Hip With Acetabular Bone Involvement: A Case Report With Radiologic‐Pathologic Correlation

Cancer Reports, Volume 9, Issue 9, September 2026.
ABSTRACT Background Diffuse‐type tenosynovial giant cell tumor (D‐TGCT) is an uncommon synovial neoplasm. Hip involvement is rare and may be difficult to recognize because symptoms are nonspecific and osseous erosion can mimic more aggressive infectious, inflammatory, or neoplastic processes.
Wang Quanbing, Xing Huanhuan, Zhang Xing, Yang Tao, Zhang Jun, Zhu Lei, Li Kai, Luo Lei, Ao Feng, Yang Wei   +9 more
wiley   +1 more source

Clinical and molecular features of primary gliosarcoma with digital spatial whole‐transcriptome analysis of glial and mesenchymal components

Brain Pathology, Volume 36, Issue 5, September 2026.
We report the clinical and genetic features of an institutional cohort of primary adult gliosarcomas compared to glioblastoma. We performed spatial whole‐transcriptome analysis on glial and sarcomatous regions of four cases to compare gene expression profiles and validated differential protein expression for two markers in tissue sections.
Matthew D. Wood, Gabriel Zangirolani, Jinho Lee, Melanie H. Hakar, Tanaya Neff, Kevin Y. Zhang, Christopher L. Corless   +6 more
wiley   +1 more source

Immunohistochemical determination of estrogen and progesterone receptor positivity in uterine adenosarcoma. [PDF]

, 2004
BACKGROUND: Given the paucity of data regarding hormone dependency, it was the purpose of this study to screen for the presence of estrogen and progesterone receptors in uterine adenosarcoma (UAS).
Schuurmans, K., Tulunay, G., Steenkiste, Edwin, Abeler, Vera M., Vergote, Ignace, Massuger, Leon, Steenkiste, E., Moerman, P., Tulunay, Gökhan, de Jonge, Eric, Amant, Frederic, Massuger, L.F.A.G., Verbist, Lieve, Moerman, Philippe, Verbist, L., Vergote, I., Schurmans, Katrien, Jonge, E. de, Abeler, V.M., Amant, F.   +19 more
core   +1 more source