Spindle cell rhabdomyosarcoma

So, it needs to be distinguished from classical forms of the neoplasm. The spindle cell variant of rhabdomyosarcoma (RMS) is uncommon and is most often encountered in the paratesticular region of children in whom it has a good prognosis. A 41-year-old nonsmoking Caucasian man presented in June 20with a painless swelling under his tongue. Sixteen cases of spindle cell RMS occurring in adults were retrieved from our files.

Jun 1 20Spindle cell rhabdomyosarcoma of the head and neck is a very rare tumor in adults. For congenitalinfantile spindle cell rhabdomyosarcoma, a study reported that of patients showed recurrent fusion genes.

What Is Rhabdomyosarcoma? - American Cancer Society

Spindle cellsclerosing histology: Spindle cellsclerosing rhabdomyosarcoma has been proposed as a separate entity in the World Health Organization Classification of Tumors of Soft Tissue and Bone. This subtype has a more favorable clinical course and prognosis than usual embryonal rhabdomyosarcoma. The spindle cell variant of embryonal rhabdomyosarcoma is a rare and a better differentiated variant of embryonal rhabdomyosarcoma, having a better prognosis compared to other types of rhabdomyosarcomas. Sep 0 20Sclerosing and spindle cell rhabdomyosarcoma is a rare histologic subtype, designated in the latest WHO classification as a stand-alone pathologic entity. May present at any age Pathology Histologically this tumor can resemble a leiomyosarcoma.

Spindle cell rhabdomyosarcoma - Spindle cell rhabdomyosarcoma is a subtype of embryonal rhabdomyosarcoma first described by Cavazzana, Schmidt and Ninfo in 1992. American Cancer Society Common sites of RMS include: The head and neck (such as near the eye, inside the nasal sinuses or throat, or near the spine in the neck) Urinary and reproductive organs (bladder, prostate glan or any of the female organs) Arms and legs. A micro tear of muscle fibers or muscle inflammation causes moderate to severe pain.

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