| Literature DB >> 8212536 |
Y Oda1, M Tsuneyoshi, H Hashimoto, T Iwashita, M Ushijima, S Masuda, Y Iwamoto, Y Sugioka.
Abstract
Primary rhabdomyosarcoma of bone is exceedingly rare. We present a case of rhabdomyosarcoma of the iliac bone in a 32-year-old male. Histologically, the tumour consisted mainly of a uniform proliferation of elongated spindle cells arranged in a herring bone pattern, simulating fibrosarcoma. Focally there was a conventional embryonal pattern with scattered rhabdomyoblasts possessing an eosinophilic cytoplasm. Immunohistochemical studies disclosed expression of muscle markers such as desmin and muscle-specific actin, in both the embryonal and spindle-cell areas and myoglobin only in the embryonal areas. Such histological features are unusual for classical embryonal rhabdomyosarcoma. The anatomical site and age of the patient are also atypical.Entities:
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Year: 1993 PMID: 8212536 DOI: 10.1007/bf01606434
Source DB: PubMed Journal: Virchows Arch A Pathol Anat Histopathol ISSN: 0174-7398