Clinicopathologic analysis of spindle cell rhabdomyosarcoma: report of 8 cases.
- Author:
Hong-Tu ZHANG
1
;
Lei GUO
;
Qin SU
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Adult; Child; Combined Modality Therapy; Desmin; metabolism; Diagnosis, Differential; Female; Follow-Up Studies; Humans; Male; Middle Aged; MyoD Protein; metabolism; Myoglobin; metabolism; Neoplasm Recurrence, Local; Retrospective Studies; Rhabdomyosarcoma, Embryonal; metabolism; pathology; surgery; Soft Tissue Neoplasms; metabolism; pathology; surgery; Young Adult
- From: Chinese Journal of Oncology 2008;30(2):141-143
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the clinicopathological features of spindle cell rhabdomyosarcoma (SCRMS) in order to differentiate it from other myosarcomas.
METHODSThe clinical features, morphologic and immunohistochemical phenotypes of 8 SCRMSs were analyzed.
RESULTSSCRMS cells were found to be arranged in a fascicular or storiform pattern, in which a number of enlarged plump or polygonal shaped rhabdomyoblasts containing abundant eosinophilic cytoplasm with eccentrically placed enlarged hyperchromatic nuclei were mixed. Immunohistochemical staining results showed that vimentin, MyoD1, desmin, actin, myoglobin were positive in tumor cells, but S-100, plap, AE1/AE3, CK, CD117 negative. The follow-up data showed that four cases had died of the recurrent disease, one still alive and the remain three patients lost follow-up.
CONCLUSIONSpindle cell rhabdomyosarcoma is a rare embryonal rhabdomyosarcoma which occurs in the childhood or adulthood with a poor prognosis, and is frequently presented as a painless mass most frequently involveing the head and neck or cervical area or para-testis site. A combination of MyoD1, desmin and myoglobin immunohistochemical staining is helpful in differential diagnosis.
