PMID- 20495536 OWN - NLM STAT- MEDLINE DCOM- 20110125 LR - 20230210 IS - 1530-0285 (Electronic) IS - 0893-3952 (Linking) VI - 23 IP - 10 DP - 2010 Oct TI - Can MDM2 analytical tests performed on core needle biopsy be relied upon to diagnose well-differentiated liposarcoma? PG - 1301-6 LID - 10.1038/modpathol.2010.106 [doi] AB - Well-differentiated liposarcoma/atypical lipomatous tumor can be difficult to differentiate from benign lipomatous tumors, especially on limited biopsy material. Adjunctive tests for MDM2 (murine double minute 2) have proven useful in whole-tissue sections; however, their utility has not been determined within the increasingly popular core needle biopsy. Herein, we compare the ability of MDM2 immunohistochemistry and MDM2 fluorescence in situ hybridization (FISH) to discriminate benign lipomatous tumors from well-differentiated liposarcoma on core needle biopsies. Well-differentiated liposarcoma (n=17) and an assortment of benign lipomatous tumors (n=37), which had concurrent or previous core needle biopsies, and resection specimens were subjected to both MDM2 immunohistochemistry and MDM2 FISH on both whole-tissue sections and corresponding core needle biopsy sections. Percentage tumor cells positive for MDM2 by immunohistochemistry and an MDM2:CEP12 FISH ratio was calculated in each biopsy and resection specimen pair and the results were compared. MDM2 FISH had a higher sensitivity (100%) and specificity (100%) compared with MDM2 immunohistochemistry (65 and 89%) in core needle biopsies, respectively. In addition, MDM2 immunohistochemistry had a false-positive rate of 11%, compared to 0% with FISH. The average MDM2:CEP12 ratio was similar in the biopsy material compared with the whole-tissue sections in both well-differentiated liposarcoma and the benign lipomatous tumor group of neoplasms. Detection of MDM2 amplification by FISH is a more sensitive and specific adjunctive test than MDM2 immunohistochemistry to differentiate well-differentiated liposarcoma from various benign lipomatous tumors, especially on limited tissue samples. FAU - Weaver, Joshua AU - Weaver J AD - Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH 44195, USA. FAU - Rao, Priya AU - Rao P FAU - Goldblum, John R AU - Goldblum JR FAU - Joyce, Michael J AU - Joyce MJ FAU - Turner, Sondra L AU - Turner SL FAU - Lazar, Alexander J F AU - Lazar AJ FAU - Lopez-Terada, Dolores AU - Lopez-Terada D FAU - Tubbs, Raymond R AU - Tubbs RR FAU - Rubin, Brian P AU - Rubin BP LA - eng PT - Comparative Study PT - Journal Article DEP - 20100521 PL - United States TA - Mod Pathol JT - Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc JID - 8806605 RN - 0 (Biomarkers, Tumor) RN - EC 2.3.2.27 (MDM2 protein, human) RN - EC 2.3.2.27 (Proto-Oncogene Proteins c-mdm2) SB - IM MH - Biomarkers, Tumor/*analysis MH - *Biopsy, Needle MH - Diagnosis, Differential MH - Humans MH - Immunohistochemistry MH - In Situ Hybridization, Fluorescence MH - Lipoma/diagnosis MH - Liposarcoma/*diagnosis/metabolism MH - Proto-Oncogene Proteins c-mdm2/*biosynthesis MH - Sensitivity and Specificity EDAT- 2010/05/25 06:00 MHDA- 2011/01/28 06:00 CRDT- 2010/05/25 06:00 PHST- 2010/05/25 06:00 [entrez] PHST- 2010/05/25 06:00 [pubmed] PHST- 2011/01/28 06:00 [medline] AID - S0893-3952(22)02636-9 [pii] AID - 10.1038/modpathol.2010.106 [doi] PST - ppublish SO - Mod Pathol. 2010 Oct;23(10):1301-6. doi: 10.1038/modpathol.2010.106. Epub 2010 May 21.