Liposarcoma differential diagnosis

Revision as of 20:22, 5 March 2019 by Ahmed Younes (talk | contribs)
Jump to navigation Jump to search

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]

Overview

Liposarcoma must be differentiated from other diseases that cause a painless, growing mass such as spindle cell lipoma, neurofibroma, dermatofibrosarcoma protuberans, and malignant peripheral nerve sheath tumor.

Differential diagnosis

Differential diagnosis of liposarcoma includes nonadipocytic lesions such as:[1]

Disease Description
Spindle cell lipoma Composed of bland, sometimes palisading, CD34-positive spindle cells, ad- mixed with eosinophilic refractile collagen bundles
Neurofibroma Characterized by a less cellular S-100– positive spindle cell proliferation with wavy nuclei
Dermatofibrosarcoma protuberans Cytologically bland, monomorphic CD34-positive spindle cell proliferation organized in a distinctive storiform growth pattern and characterized by tendency to infiltrate the surrounding fat in a peculiar ‘‘honeycomb’’ pattern
Malignant peripheral nerve sheath tumor Generally highly cellular tumors composed of tapering or wavy spindle cells featuring perivascular accentuation and focal S-100– positive immunoreactivity in approximately 50% of cases[1]
Disease Clinical feature Laboratory findings Imaging findings
Fever Weight loss Abdominal pain
Retroperitoneal hematoma Anemia MRI is the best radiologic tool to differentiate between retroperitoneal masses.
Retroperitoneal abscess Leukocytosis, positive inflammatory markers
Retroperitoneal tumors (.e.g. liposarcoma) positive tumor marker
Chronic pancreatitis DM type II, amylase and lipase levels may be slightly elevated

References

  1. 1.0 1.1 Dei Tos AP (2000). "Liposarcoma: new entities and evolving concepts". Ann Diagn Pathol. 4 (4): 252–66. doi:10.1053/adpa.2000.8133. PMID 10982304.


Template:WikiDoc Sources