Liposarcoma differential diagnosis: Difference between revisions
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==Differential diagnosis== | ==Differential diagnosis== | ||
Differential diagnosis includes nonadipocytic lesions such as | Differential diagnosis of liposarcoma includes nonadipocytic lesions such as:<ref name="pmid10982304">{{cite journal| author=Dei Tos AP| title=Liposarcoma: new entities and evolving concepts. | journal=Ann Diagn Pathol | year= 2000 | volume= 4 | issue= 4 | pages= 252-66 | pmid=10982304 | doi=10.1053/adpa.2000.8133 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10982304 }} </ref> | ||
*Inflammatory myofibroblastic tumor | |||
*Castleman’s disease | |||
*[[Lipoma|Spindle cell lipoma]] | |||
*[[Neurofibroma]] | |||
*[[Dermatofibrosarcoma protuberans]] | |||
*[[Malignant peripheral nerve sheath tumor]] | |||
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Revision as of 17:07, 25 August 2015
Liposarcoma Microchapters |
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Liposarcoma differential diagnosis On the Web |
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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]
- Inflammatory myofibroblastic tumor
- Castleman’s disease
- Spindle cell lipoma
- Neurofibroma
- Dermatofibrosarcoma protuberans
- Malignant peripheral nerve sheath tumor
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] |
References
- ↑ 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.