Precursors to neuroblastoma recurrence

Written by Chen Yu Fei
Neurosurgery
Updated on September 28, 2024
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For neuroblastoma, if recurrence occurs, the patient may show symptoms like recurrent headaches, dizziness, nausea, and vomiting. Additionally, if the optic nerve is involved, there may be a decrease in vision and visual field defects. Even the possibility exists that the tumor could recur, increase in size, and compress surrounding important blood vessels and nerves, leading to an increase in intracranial pressure, which manifests as worsening of the original symptoms of headaches and dizziness. Once such symptoms occur, it generally suggests a high likelihood of neuroblastoma recurrence. If it causes symptoms such as hemiplegia and aphasia, it can generally be confirmed.

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Written by Chen Yu Fei
Neurosurgery
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Neuroblastoma is what disease

Neuroblastoma is a highly malignant epithelial neurocyte tissue tumor, which is relatively aggressive. Often in the early stages of the disease, the tumor tissue adheres to surrounding brain tissue, nerves, and blood vessels, making it impossible to completely remove it surgically. The residual tumor cells quickly recur over time. As a result, most neuroblastoma patients have a poor prognosis and short survival time, even with effective surgical treatment, including postoperative radiotherapy and chemotherapy. Therefore, it is recommended that those diagnosed with neuroblastoma undergo early further examinations and treatments.

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Written by Chen Yu Fei
Neurosurgery
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Can neuroblastoma be cured?

Neuroblastoma is a malignant tumor that often grows rapidly. In the early stages of the disease, it can easily invade surrounding tissues and nerves, making it very difficult to completely remove the tumor through surgery. In most cases, even after surgical treatment, there is a high tendency for recurrence in children, making it difficult to achieve a clinical cure. For most patients with neuroblastoma, early post-surgical treatment involving high doses of radiotherapy and chemotherapy can effectively reduce the likelihood of tumor recurrence and appropriately prolong the patient’s lifespan. This helps in extending the lifespan and improving the quality of life to some extent, but generally, the final prognosis remains poor.

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Written by Chen Yu Fei
Neurosurgery
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Precursors to neuroblastoma recurrence

For neuroblastoma, if recurrence occurs, the patient may show symptoms like recurrent headaches, dizziness, nausea, and vomiting. Additionally, if the optic nerve is involved, there may be a decrease in vision and visual field defects. Even the possibility exists that the tumor could recur, increase in size, and compress surrounding important blood vessels and nerves, leading to an increase in intracranial pressure, which manifests as worsening of the original symptoms of headaches and dizziness. Once such symptoms occur, it generally suggests a high likelihood of neuroblastoma recurrence. If it causes symptoms such as hemiplegia and aphasia, it can generally be confirmed.

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home-news-image
Written by Chen Yu Fei
Neurosurgery
40sec home-news-image

Symptoms of neuroblastoma recurrence

For neuroblastoma, when the tumor recurs, the patient's original symptoms such as headaches, dizziness, nausea, and vomiting will reappear, occurring intermittently and worsening persistently. Most patients will experience significant increased intracranial pressure, and even frequent nausea and vomiting. Additionally, some neuroblastoma patients experience severe vertigo, especially when changing body positions, where the vertigo is particularly pronounced. For such patients, when the above symptoms and signs occur, they should go to a local hospital as soon as possible for a reassessment using cranial MRI to monitor changes in their condition.

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Written by Chen Yu Fei
Neurosurgery
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Age of onset of neuroblastoma

Neuroblastoma, typically arises from primitive neural crest cells, is more commonly found in the sympathetic ganglia and adrenal medulla. There is no specific age for the onset of neuroblastoma, but research indicates that it is more commonly diagnosed in children. The exact causative factors of neuroblastoma are not yet fully understood, but it is widely believed to involve congenital genetic factors, including acquired genetic mutations. Clinically, the presentation largely depends on the location of the tumor, the age at diagnosis, and the degree of malignancy of the tumor. In most cases, the tumor originates in the abdominal cavity, with a higher occurrence in the adrenal glands in children.