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Volume 37, Issue 3, Pages 312-321 (March 2006)


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Calretinin expression in tumors of adipose tissue

Justin M.M. Cates, MD, PhDaCorresponding Author Informationemail address, Bryan N. Coffing, MDb, Brent T. Harris, MD, PhDc, Candice C. Black, DOc

Received 1 September 2005; received in revised form 8 November 2005; accepted 9 November 2005. published online 23 January 2006.

Summary 

Although well established as a marker of mesothelial cells, calretinin is also expressed in several other tissue types, including adipose tissue. Accordingly, immunohistochemical staining for calretinin has been described in an increasing number of neoplasms other than mesothelioma. A detailed analysis of calretinin expression in lipogenic tumors has not yet been reported, however. Given the known expression patterns of calretinin in normal tissues, we predicted that calretinin immunoreactivity would be detected in lipoma and the various histologic subtypes of liposarcoma, and that this marker might be of use in the differential diagnosis of selected fatty tumors. A variety of pleomorphic and small round cell sarcomas were studied for comparison. Calretinin immunoreactivity was detected, at least focally, in all 10 samples of normal adipose tissue and in 22 of 23 lipomas or lipoma variants. Staining for calretinin was also positive within the lipogenic component of 28 of 29 liposarcoma variants. Of the 7 dedifferentiated liposarcomas, 3 were focally positive for calretinin. Pleomorphic variants of other sarcomas, including undifferentiated high-grade pleomorphic sarcoma, rhabdomyosarcoma, leiomyosarcoma, and malignant peripheral nerve sheath tumor also exhibited focal calretinin immunoreactivity in a minority of cases, as did some small round cell sarcomas. These results suggest that calretinin immunoreactivity in normal and neoplastic adipose tissue is more ubiquitous than previously reported and may be a useful, albeit nonspecific marker of lipogenic differentiation. However, its utility in the differential diagnosis of fatty tumors appears limited.

a Department of Pathology, Vanderbilt University Medical Center and Vanderbilt University School of Medicine, Nashville, TN 37232, USA

b Department of Pathology, University of Michigan Health System, Ann Arbor, MI 48109, USA

c Department of Pathology, Dartmouth Hitchcock Medical Center and Dartmouth Medical School, Lebanon, NH 03756, USA

Corresponding Author InformationCorresponding author.

 The Research Pathology Division at Dartmouth Hitchcock Medical Center, Lebanon, NH, provided the financial and technical support for this study.

PII: S0046-8177(05)00636-2

doi:10.1016/j.humpath.2005.11.006


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