How does neuroblastoma heal itself?

Written by Chen Yu Fei
Neurosurgery
Updated on September 03, 2024
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Neuroblastoma cannot completely heal by itself. Once neuroblastoma is detected, patients should be promptly taken to local hospitals for treatment, be hospitalized, and undergo skull CT or MRI scans. If necessary, enhanced MRI scans can be conducted to clarify the current location of the tumor and its relationship with surrounding tissues, and to determine the surgical plan. The tumor should be completely removed through surgery. After the surgery, a small amount of tumor tissue should be kept for pathological slides to assess the need for radiotherapy, chemotherapy, or other related treatments based on the results of the pathological examination. For some elderly and frail patients who cannot tolerate surgery, Gamma Knife treatment can also be considered.

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Written by Chen Yu Fei
Neurosurgery
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Late-stage symptoms of neuroblastoma

For patients with neuroblastoma, they often experience significant symptoms such as headaches, dizziness, nausea, and vomiting. The intracranial pressure continuously rises, leading to noticeable optic atrophy, vision loss, and visual field defects. When the tumor volume further increases, it may also compress the surrounding tissues, causing apparent cranial nerve dysfunction. Moreover, in the late stages of the disease, the tumor can spread to other parts of the body via the bloodstream, forming metastases. Additionally, it is likely to disseminate through the cerebrospinal fluid.

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Written by Chen Yu Fei
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How is neuroblastoma diagnosed?

For patients with neuroblastoma, diagnosis is primarily through the symptoms, signs, detailed physical examinations, medical history inquiries, and most importantly, radiological data, which includes CT scans or MRI of the head. Definitive diagnosis requires surgical removal of the tumor. A small amount of tumor tissue is retained after excision and used for pathological examination to confirm the diagnosis. Neuroblastoma is categorized as an epithelial-like malignant tumor, indicative of a high degree of malignancy. In most cases, early in the disease, the tumor adheres to surrounding tissues, which greatly complicates complete surgical removal, and most patients have a poor prognosis.

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Causes of Neuroblastoma

Currently, there is no definitive conclusion about the specific causes of neuroblastoma, but most scholars believe that the occurrence of neuroblastoma is the result of congenital genetic factors combined with acquired factors. For patients with neuroblastoma, there is often a family history of genetic diseases showing a familial clustering tendency. In addition, poor living environments and habits, including exposure to radioactive contamination or prolonged exposure to electromagnetic radiation, may also contribute to the development of neuroblastoma.

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Early symptoms of neuroblastoma

For neuroblastoma, in the early stages of the disease, mild headaches, dizziness, nausea, and vomiting often occur, but the symptoms are relatively mild and most can be tolerated. As the disease gradually progresses and the tumor volume begins to increase, it compresses the surrounding brain tissue and cranial nerves, causing the patient to exhibit certain degrees of headache, dizziness, nausea, vomiting, and other clinical manifestations. As the tumor volume further increases and cerebral edema becomes apparent with elevated intracranial pressure, it may lead to cranial nerve dysfunction in patients. For instance, it might trigger epileptic seizures or cause patients to experience hemiplegia, aphasia, and other clinical manifestations. Once these symptoms occur, it is advisable to visit a local hospital early for treatment.

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Written by Chen Yu Fei
Neurosurgery
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Is neuroblastoma serious?

Neuroblastoma is relatively serious and is classified as a highly malignant tumor, one of the epithelial cell tumors. The disease often leads to severe intracranial pressure increases, manifesting as intense headaches, dizziness, nausea, vomiting, and even possible optic disc edema, vision loss, and visual field defects. The occurrence of neuroblastoma often indicates a poor prognosis for patients, with a short disease duration and reduced survival time. The five-year survival rate is decreased. Treatment primarily involves surgical intervention to completely remove the neuroblastoma, followed by postoperative radiotherapy, chemotherapy, and other related treatments.