Liposarcoma diagnostic study of choice
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Sabawoon Mirwais, M.B.B.S, M.D.[2]
Overview
The optimal method for diagnosis of liposarcoma is by biopsy. Biopsy also provides important histopathological information required to identify the sub-type of the liposarcoma.
Diagnostic Study of Choice
Study of Choice
The optimal method for diagnosis of liposarcoma is by biopsy. Biopsy also provides important histopathological information required to identify the sub-type of the liposarcoma.
Subtype | Findings |
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Atypical lipomatous neoplasm (ALN)/Well-differentiated liposarcoma (WDL) | 4 subtypes: Multivacuolated lipoblasts and spindle cells with hyperchromatic nuclei are often observed. |
De-differentiated liposarcoma | Abrupt transition from a low-grade to a high-grade differentiation within the same mass of a well-differentiated liposarcoma. |
Myxoid liposarcoma | Multinodular mass with round cells and hyaluronic acid matrix. High cellularity at the periphery and low cellularity at the center of the mass. Mitotic activity is normal and the nuclei are normochromatic. |
Pleomorphic liposarcoma | Pleomorphic lipoblasts with hyperchromatic nuclei, acidophilic cytoplasm, and eosinophilic hyaline globules. Spindle cells and multinucleated giant cells may be observed. |
Mixed-type liposarcoma | Mixed features of myxoid, pleomorphic, and well-differentiated liposarcoma. |
Table adapted from Fletcher CDM, Unni KK, Mertens F, eds. World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone. Geneva:IARC Press; 2002[1] and Enzinger and Weiss's Soft Tissue Tumors , 6th Edition [2] |
Staging
The staging of liposarcoma is based on the TNM classification, which includes primary tumor spread, lymph node involvement, and presence of metastasis.
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Stages | Primary Tumor (T) | Lymph Node (N) | Metastasis (M) | Histopathological Grading |
Stage IA | T1a, T1b | N0 | M0 | Low grade |
Stage IB | T2a, T2b | N0 | M0 | Low grade |
Stage IIA | T1a, T1b | N0 | M0 | High grade |
Stage IIB | T2a, T2b | N0 | M0 | High grade |
Stage III | Any T | N0, N1 | M0 | High grade |
Stage IV | Any T | Any N | M1 | Any grade |
Retrieved from the National Cancer Institute. Adapted from AJCC: Soft tissue sarcoma. In: Edge SB, Byrd DR, Compton CC, et al., eds.: AJCC Cancer Staging Manual. 7th ed. New York, NY: Springer, 2010, pp 291-8.[3] |
References
- ↑ Fletcher, Christopher (2002). Pathology and genetics of tumours of soft tissue and bone. Lyon: IARC Press. ISBN 9283224132.
- ↑ Goldblum, John (2014). Enzinger and Weiss's soft tissue tumors. Philadelphia, PA: Saunders/Elsevier. ISBN 978-0-323-08834-3.
- ↑ 3.0 3.1 3.2 3.3 "National Cancer Institute - Stage Information for Adult Soft Tissue Sarcoma".