What should be avoided in the diet for neuroblastoma?

Written by Chen Yu Fei
Neurosurgery
Updated on September 10, 2024
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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
Neurosurgery
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How to avoid neuroblastoma

To avoid neuroblastoma, it is recommended to develop good living habits in daily life, including maintaining over 30 minutes of aerobic exercise each day to keep physically healthy. Additionally, it is advisable to consume more fruits rich in vitamin C, which contain abundant vitamins that can effectively serve as antioxidants. Keeping good sleep habits, going to bed early and waking up early, avoiding staying up late and long durations of using mobile phones or computers to minimize excessive exposure to electromagnetic radiation. In daily life, one should also learn self-protection, avoid contact with carcinogenic chemicals, and avoid excessive exposure to radioactive pollution. All these measures can effectively prevent the condition.

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Written by Chen Yu Fei
Neurosurgery
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Early symptoms of neuroblastoma

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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Neuroblastoma treatment

Neuroblastoma is relatively considered a malignant tumor, and its growth rate is quite rapid. It often adheres to surrounding tissues in the early stages, which makes it very difficult to completely remove surgically. However, even so, it is still advisable to opt for surgical treatment once neuroblastoma is detected. The tumor should be completely removed surgically, and a small amount of tumor tissue should be retained for pathological examination after removal. Based on the results of the pathological examination, it will be determined whether additional treatments such as radiotherapy or chemotherapy are needed. Furthermore, since some neuroblastomas are sensitive to radiotherapy, it is recommended to promptly take the patient to a local hospital for treatment after surgery.

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Written by Chen Yu Fei
Neurosurgery
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How to check for neuroblastoma?

For the examination of neuroblastoma, we generally recommend a neurological examination to help determine whether there are any clear positive signs, as well as to inquire about medical history and family history to judge if there are any cases of neuroblastoma among family members. Additionally, detailed laboratory tests, routine blood tests, routine urine tests, and biochemical tests, including tumor-related diagnostics, can help in making assessments. Of course, the most accurate and crucial examinations are CT or MRI scans of the head. If necessary, an enhanced MRI scan of the head can be conducted to further evaluate the location, nature, severity of the tumor, and its relationship with the surrounding neural and vascular tissues, which helps provide a basis for further surgical treatment.

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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.