Beyond the benign: A rare case report of myxoid pleomorphic liposarcoma

Myxoid pleomorphic liposarcoma is a rare and aggressive subtype of soft tissue sarcomas (STS). It primarily arises from adipose tissue and exhibits a high rate of recurrence and metastatic potential. We report the case of a 35-year-old male gym trainer with a 5-month history of a painless, progressively enlarging mass on the right posterior aspect of chest, diagnosed with myxoid pleomorphic liposarcoma following imaging and histopathological evaluation of the excised specimen. Surgical excision with clear margins and adjuvant radiotherapy resulted in a favorable outcome with no recurrence at 7 months. This case emphasizes the importance of early diagnosis and multidisciplinary approach in managing a rare soft tissue sarcoma to prevent complications from a delayed intervention.

Authors

Institutions

Publication Details

Journal
Radiology Case Reports
Published
2025-03-08
DOI
https://doi.org/10.1016/j.radcr.2025.01.056
Citations
1
Primary Topic
Sarcoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
1.52
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Beyond the benign: A rare case report of myxoid pleomorphic liposarcoma

Arslan Ahmed, Muhammad Ammar, Rana Uzair Ahmad, Muhammad Sadiq et al.
1 citations
Radiology Case Reports
Sarcoma Diagnosis and Treatment
1.52
article

Beyond the benign: A rare case report of myxoid pleomorphic liposarcoma

Arslan Ahmed, Muhammad Ammar, Rana Uzair Ahmad, Muhammad Sadiq, Nouman Aziz, Muhammad Hasnain Saleem Choudary
article en
1 citations

Abstract

Myxoid pleomorphic liposarcoma is a rare and aggressive subtype of soft tissue sarcomas (STS). It primarily arises from adipose tissue and exhibits a high rate of recurrence and metastatic potential. We report the case of a 35-year-old male gym trainer with a 5-month history of a painless, progressively enlarging mass on the right posterior aspect of chest, diagnosed with myxoid pleomorphic liposarcoma following imaging and histopathological evaluation of the excised specimen. Surgical excision with clear margins and adjuvant radiotherapy resulted in a favorable outcome with no recurrence at 7 months. This case emphasizes the importance of early diagnosis and multidisciplinary approach in managing a rare soft tissue sarcoma to prevent complications from a delayed intervention.

Radiology Case ReportsVol. 20(5)
Mayo Hospital (PK)
Zero hunger
Openalex Percentile: Top 21%
Sarcoma Diagnosis and Treatment
1.52
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.