Volume 12, Issue 6 pp. 476-485
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Cutaneous extraskeletal Ewing's sarcoma

M. S. Peters

M. S. Peters

Departments of Dermatology, Mayo Foundation, Rochester, Minnesota, USA

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H. M. Reiman

H. M. Reiman

Departments of Pathology, Mayo Clinic and Mayo Foundation, Rochester, Minnesota, USA

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S. A. Muller

Corresponding Author

S. A. Muller

Departments of Dermatology, Mayo Foundation, Rochester, Minnesota, USA

Dr. S. A. Mullar, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, U.S.A.Search for more papers by this author
First published: December 1985
Citations: 23

Abstract

Extraskeletal Ewing's sarcoma has been recognized as being histologically indistinguishable from Ewing's sarcoma of bone. Although the occurrence of extraosseous Ewing's sarcoma in deep soft tissues has been well described, such cutaneous lesions arc rare. We report the clinical history, histopathologic findings, and results of ultrastructural study of this rare variant occurring in a 12-year-old girl. She presented with a dermal and subcutaneous tumor of the left third toe, without osseous involvement. The lesion was composed of masses of round-oval cells, with perilobular fibrosis, focal hemorrhage, ill-defined pale cytoplasm containing glycogen, and absent pericellular reticulin. Ultrastructural study showed a monotonous cell population, with focal thickening of apposing membranes, high nuclear/cytoplasmic ratio, copious intracytoplasmic glycogen, and paucity of organ cells except mitochondria. We present this case along with discussion of the literature and problems concerning differential diagnosis of small cell malignancies in the skin.

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