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A Primitive Neuroectodermal Tumor and Social Security

Cancer is far more than a single disease. Cancer is a large group of disorders. These diseases are evidenced by cells that are invasive (they invade and destroy adjacent tissue), aggressive (they divide and grow without respect to normal limits) and sometimes metastatic (they move to other areas of the body). There are many different forms of cancer. They are usually named by where they start in your body. For example, pancreatic cancer begins in your pancreas. Esophageal cancer originates in your esophagus. Cancer may often spread to other places in your body, but it is still called by where it started. Cancer is also classified by the type of cell that the tumor looks like. Some examples of this are lymphoma, carcinoma, blastic tumor, sarcoma and germ cell tumor. A primitive neuroectodermal tumor is one of a group of cancers that shares certain genetic and biochemical features and arises from the same kind of early cells as a family of cancers that are known as Ewing’s sarcoma. Ewing’s sarcoma usually originates in your bone, while a primitive neuroectodermal tumor usually begins in your soft tissue. If you have been diagnosed with a primitive neuroectodermal tumor, this may enable you to receive social security disability benefits like SSDI or SSI. A wise decision is to consult the social security attorneys at disabilitycasereview.com to find out the options that are available to you. The social security attorneys at disabilitycasereview.com are experienced in matters involving disability benefits. Go to disabilitycasereview.com, today. In many instances, a primitive neuroectodermal tumor will develop in your central nervous system and brain. In other cases, a primitive neuroectodermal tumor may take place in areas outside of your brain, such as your chest wall, pelvis or limbs. Fortunately, a primitive neuroectodermal tumor is rare in the United States. A primitive neuroectodermal tumor is responsible for somewhere around 25% of the brain tumors that take place in children. Around 8 out of every 1 million children are affected by a primitive neuroectodermal tumor each year in the United States. Most of the time, this tumor takes place in children or adults who are under the age of 25. A primitive neuroectodermal tumor is brought about by cells that mutate and begin to multiply and grow out of control. However, no one has yet discovered why this starts to take place. It is believed by researchers that genetics may play a significant role is leading to this form of cancer. There are several different signs and symptoms that may be produced by a primitive neuroectodermal tumor. Some of the possible signs and symptoms are:
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