Results 71 to 80 of about 14,551 (185)

Paratesticular Embryonal Rhabdomyosarcoma Masquerading as Epididymitis: A Diagnostic Challenge in Adolescents

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Paratesticular rhabdomyosarcoma is a rare malignancy in children and adolescents that frequently presents diagnostic challenges when mimicking benign inflammatory conditions. We report the case of a 14‐year‐old previously healthy male who presented with acute right scrotal pain and swelling initially diagnosed as epididymo‐orchitis.
Saif Khaled Abdalhadi Azzam, Lina Barhoum Barhoum, Ammir Abuzahra, Alaa Alazzeh, Khader Hassouneh, Nour Aldin K. Fakhory, Mohd Othman Lafi, M. I. Jawabreh Issa, Ibrahim Alzatari, Hamza Zughaier   +9 more
wiley   +1 more source

Hypofractionated preoperative radiotherapy for extremity soft tissue sarcoma: Are we racing ahead of the toxicity data?

Cancer, Volume 132, Issue 15, 1 August 2026.
ABSTRACT For patients who have localized, high‐risk soft tissue sarcoma of the extremity, combined‐modality local treatment with radiation therapy (RT) and surgery offers high rates of local control. When RT is used, preoperative RT is recommended. The current standard of care dosing is 50 Gray (Gy) conventionally fractionated, delivered as 2 Gy per ...
Kilian E. Salerno, Denise Reinke, Kathrin Schuster, B. Ashleigh Guadagnolo   +3 more
wiley   +1 more source

A subset of high‐grade sarcomas with myogenic differentiation are associated with recurrent FGFR fusions

The Journal of Pathology: Clinical Research, Volume 12, Issue 4, July 2026.
Abstract Recurrent fusions involving FGFR1‐4 genes have been previously described in rare subsets of mostly benign chondroid and mesenchymal neoplasms involving bone and soft tissue. However, a more comprehensive analysis of sarcomas associated with FGFR fusions, including their incidence and histotypes, has not been performed.
Maximus CF Yeung, Carla Saoud, Sarah Chiang, Meera Hameed, Cristina R Antonescu   +4 more
wiley   +1 more source

Myxoid pleomorphic liposarcoma : a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pleomorphic liposarcoma

, 2021
Myxoid pleomorphic liposarcoma is a recently defined subtype of liposarcoma, which preferentially involves the mediastinum of young patients and shows mixed histological features of conventional myxoid liposarcoma and pleomorphic liposarcoma.
Menten, Björn, Van Dorpe, Jo, Raman, Lennart0001102304938020026391439769702627760000-0002-3840-593039E4304E-F0EE-11E1-A9DE-61C894A0A6B4, Ferdinande, LiesbethGE32UZGent00199621513680100176606300FFA574-F0EE-11E1-A9DE-61C894A0A6B4, Van Dorpe, JoGE32UZGent8020018760750000-0001-8175-2930B7E2A26E-49B6-11E4-AA90-F166B5D1D7B1, Van der Linden, Malaïka, Raman, Lennart, Flucke, Uta, Menten, BjörnGE31UZGent0019961997768010017113010000-0001-8182-659XF6A4B240-F0ED-11E1-A9DE-61C894A0A6B4, Folpe, Andrew L., Koelsche, Christian, van Gorp, Joost M., Fritchie, Karen, von Deimling, Andreas, Ferdinande, Liesbeth, Creytens, David, Mentzel, Thomas, Creytens, DavidGE32UZGent0001313716458020013460130000-0002-6064-16739E10BFB8-1EEF-11E2-A298-0C6810BDE39D, Van der Linden, MalaïkaGE32UZGent0001008017908020021166560000-0003-0249-908X2F90553C-F0EE-11E1-A9DE-61C894A0A6B4   +18 more
core   +1 more source

Rare Late Cardiac Involvement Following Resected Primary Limb Dedifferentiated Liposarcoma: A Case Report

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Dedifferentiated liposarcoma (DDLPS) is a rare and aggressive subtype of soft tissue sarcoma, most commonly arising in the extremities or retroperitoneum. Cardiac involvement, whether primary or metastatic, is exceedingly rare and presents significant diagnostic and therapeutic challenges.
Azin Alizadehasl, Saeedeh Baghyari, Mostafa Salimi   +2 more
wiley   +1 more source

Myxoid Liposarcoma of the Spermatic Cord

, 2005
The myxoid liposarcoma, a rare form of spermatic cord liposarcoma, is a neoplasia of adult men which arise from adipose tissue, with a slow and subdolous growth, showing good prognosis and low incidence of local or distant recurrence.
D. Masala, G. Perugia, D. Di Viccaro, M. Liberti, L. Iaboni, S. Teodonio   +5 more
core   +1 more source

Characteristics of Liposarcoma Patients: 5-Year Data

Althea Medical Journal, 2018
Background: Liposarcoma is the second highest soft tissue sarcoma in adults with prevalence of 15% to 25%. If the size of liposarcoma is very large, it may cause abdominal pain, weight loss, gastrointestinal bleeding, even kidney failure.
Miftahur Rahmah, Afiati Afiati, Unwati Sugiri   +2 more
doaj   +1 more source

An inguinal enigma: Myxoid liposarcoma in a female

, 2023
Myxoid liposarcoma of the inguinal region is rare, can mimics an inguinal hernia. Any swelling in the inguinal region, that is partially reducible, fluctuant, soft, and without any signs of bowel obstruction should be evaluated ...
Pawan Lal, Meeta Singh, Sripooja Makthala, Shantanu Agarwal, Lovenish Bains   +4 more
core   +1 more source

Survival and prognostic factors among different types of liposarcomas based on SEER database

Scientific Reports
The aim of this study is to elucidate the disparities in survival and risk factors among different subtypes of liposarcoma, through analysis of epidemiological and prognostic data.
Jiaqi Zhao, WenLi Du, XiaoLiang Tao, AiAi Li, Yi Li, Shuai Zhang   +5 more
doaj   +1 more source

Perineal myxoid liposarcoma: report of a case and literature review [PDF]

, 2010
Liposarcomas are rare soft tissue tumour, with an incidence of 30 cases per million population. The myxoid liposarcoma (MLS) consists of 45 – 55% of these tumours, making it the most common subtype. MLS commonly involves the thigh and retroperitoneum but
Mat Hassan, Mohd. Zailani, Mohd Yusof, Mubarak, Ramasamy, Prabhu, Md Nor, Azmi, Harun, Norra   +4 more
core