Diagnostic Histopathology
Volume 14, Issue 11 , Pages 552-562, November 2008

Myoepithelial tumours of skin and soft tissue: an update

Briana C Gleason MD is at the Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA

Jason L Hornick MD PhD is at the Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA

published online 03 October 2008.

Abstract 

Over the past decade, myoepithelial neoplasms have been recognized to arise primarily in skin and soft tissue. Similar to their salivary gland counterparts, owing to the plasticity of myoepithelial cells, these tumours show considerable cytological and architectural heterogeneity. Recognition of these uncommon neoplasms can be challenging, and a broad differential diagnosis may be considered. Criteria for malignancy in myoepithelial tumours of soft tissue have recently been established and are essentially cytological in nature, in contrast to the criteria used in salivary gland neoplasms. Myoepithelial carcinomas of soft tissue appear to be overrepresented in the paediatric population, in whom an aggressive clinical course is common. Whereas some cutaneous myoepitheliomas are similar to those in soft tissue, a distinctive ‘syncytial variant’ comprises at least 50% of dermal cases. This review will examine the pathological features, clinical behaviour and differential diagnosis of myoepithelial tumours of skin and soft tissue.

Keywords: chondroid syringoma, myoepithelioma, myoepithelial carcinoma, sarcoma, soft tissue neoplasms, skin neoplasms

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PII: S1756-2317(08)00153-9

doi:10.1016/j.mpdhp.2008.08.005

Diagnostic Histopathology
Volume 14, Issue 11 , Pages 552-562, November 2008