How to diagnose neuroblastoma?

Written by Chen Yu Fei
Neurosurgery
Updated on January 22, 2025
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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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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 Gao Yi Shen
Neurosurgery
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Is neuroblastoma hereditary?

Neuroblastoma has a partial genetic predisposition, but current research has not definitively determined the extent or probability of its heritability. For modern neuroblastoma, its origin is primarily associated with genetic mutations or chromosomal changes. Factors such as smoking, drinking, and drug use by the mother during pregnancy can severely harm the fetus and potentially lead to the development of neuroblastoma. Sometimes, excessive radiation or the misuse of certain drugs can also cause neuroblastoma. Therefore, while there is a certain genetic tendency for neuroblastoma, it is not the main factor.

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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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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.

doctor image
home-news-image
Written by Chen Yu Fei
Neurosurgery
50sec home-news-image

How does neuroblastoma heal itself?

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.