Early symptoms of neuroblastoma

Written by Chen Yu Fei
Neurosurgery
Updated on September 25, 2024
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For patients with neuroblastoma, the early stages of the disease often manifest as mild headaches, dizziness, nausea, and vomiting. The symptoms are relatively mild and can be significantly alleviated by taking oral pain relief medications. Therefore, the condition often does not receive adequate attention, leading to missed diagnoses. As the tumor size increases, the original symptoms such as headaches and dizziness will significantly worsen. Some patients may even experience optic nerve atrophy, papilledema, reduced visual fields, and vision deficits. When such conditions occur, patients often undergo cranial CT or MRI scans to confirm the presence of neuroblastoma.

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Written by Chen Yu Fei
Neurosurgery
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What should be avoided in the diet for neuroblastoma?

Patients with neuroblastoma should be cautious with their diet and avoid foods that are overly greasy or spicy. It's also advisable to limit or avoid carbohydrate-rich or fried foods and those high in cholesterol. If the patient has allergies, they should avoid seafood products, which contain abundant animal proteins and can trigger allergic reactions, potentially leading to allergic dermatitis or allergic asthma. Additionally, some fruits, such as durian or mango, may also induce allergic reactions, so it is best to consume them sparingly or not at all.

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Written by Chen Yu Fei
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Causes of Neuroblastoma

Neuroblastoma is a highly malignant tumor. In most cases, it is seen in neuroepithelial cells. Currently, there is no consensus on the specific causes of neuroblastoma. It is generally believed that congenital genetic factors, as well as mutations, gene deletions, and changes in tumor suppressor genes in patients, are greatly related. Acquired factors should not be ignored either, such as poor lifestyle and dietary habits. In most cases, the prognosis for neuroblastoma is poor, with patients having a short survival period. Most patients, even after undergoing surgical treatment, often experience poor outcomes and ultimately die from multi-organ dysfunction and failure.

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Written by Chen Yu Fei
Neurosurgery
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How to diagnose neuroblastoma?

For neuroblastoma, the final diagnosis requires the patient to undergo surgical treatment. During the surgery, the neuroblastoma is completely excised, and a small amount of tumor tissue is retained for pathological sectioning. The diagnosis is determined based on the results of the pathological examination, which assesses the specific cells of the neuroblastoma, whether it is benign or malignant, and its level of malignancy. This also determines how the patient will receive subsequent treatments like radiotherapy and chemotherapy. In addition to relying on pathological examinations, most neuroblastoma patients can also undergo more thorough examinations. In most cases, elevated levels of catecholamines and their metabolites can be found in the blood or urine of neuroblastoma patients, significantly higher than that of the normal population.

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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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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.