But, in fact, one died, one developed a benign tumor and the two others showed permanent inflammation of tissues.

They first tested whether the tumours showed amplification of Mdm2.

In 95% of cases the tumor will not show any signs of growth after a 4 to 6 year period.

Treatment for most children whose tumors do not show these genetic changes includes surgery to remove the tumor when possible.

The authors further found once they performed survival analyses that tumors belonging to the various groups showed significantly different outcomes when treated uniformly.

These tumors tend to involve the entire extent of the nerve and show a strong autosomal dominant inheritance.

These tumours showed an exclusive or prominent enterochromaffin like cell population.

After this therapy, tumors showed an apparent growth delay.

However, irrespective of histologic type, these tumors almost never show necrosis or increased mitoses.

Nearly all tumors show short to more sweeping fascicles of spindled rhabdomyoblasts.