You could be reading the full-text of this article now if you...

If you have access to this article through your institution,
you can view this article in

Cutaneous Clear Cell Sarcoma: Report of Three Cases of a Potentially Underestimated Mimicker of Spindle Cell Melanoma

Falconieri, Giovanni MD*; Bacchi, Carlos E. MD, PhD; Luzar, Bostjan MD, PhD

American Journal of Dermatopathology:
doi: 10.1097/DAD.0b013e3182473190
Brief Report
Abstract

Abstract: Clear cell sarcoma is a unique soft tissue tumor with distinct microscopic features that include a nested or fascicular pattern of spindle cells accompanied by larger wreath-like giant cells scattered throughout. It harbors a unique EWSR1-ATF1 gene fusion secondary to a t(12;22)(q13;q12) translocation. Recently, it was reported that clear cell sarcoma can occur in the skin and mimic a broad spectrum of entities, including spindle cell melanoma. Here, we describe 3 new cases of clear cell sarcoma of the skin, all of which were confirmed molecularly. The patients, a 12-year-old boy, a 29-year-old woman, and a 60-year-old man, had cutaneous lesions on the thigh, dorsum of foot, and sole, respectively. All 3 lesions were originally considered suspicious of spindle cell melanoma. Microscopically, the lesions featured nodular proliferation centered in the dermis that consisted of discrete fascicles of spindle cell enmeshed by thin fibrous strands. Wreath-like cells were present in all cases. Tumor cells were positive for S100 protein (3 of 3 cases), melan A (2 of 3 cases), HMB 45 (1 of 3 cases) although a junctional melanocytic proliferation was seen in 1 case. Sentinel lymph node biopsy was negative in 2 patients. Follow-up was uneventful in 2 patients, whereas the other patient developed a lymph node metastasis 5 months after primary tumor excision. This study confirms that malignant dermal tumors that mimic but do not exactly replicate spindle cell melanoma should raise suspicion for cutaneous clear cell sarcoma and prompt the investigation for the confirmatory gene fusion t(12;22).

Author Information

*Department of Pathology, General Hospital S. Maria Della Misericordia, Udine, Italy

Consultoria em Patologia, Botucatu, Sao Paulo, Brazil

Institute of Pathology, Medical Faculty, University of Ljubljana, Ljubljana, Slovenia.

Reprints: Giovanni Falconieri, MD, Department of Pathology, General University Hospital, S. Maria Della Misericordia, I 33100 Udine, Italy (e-mail: Falconieri.Giovanni@aoud.sanita.fvg.it).

The authors state that they have no funding or conflict of interest to disclose.

© 2012 Lippincott Williams & Wilkins, Inc.