Early symptoms of neuroblastoma

Written by Chen Yu Fei
Neurosurgery
Updated on January 09, 2025
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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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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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Written by Chen Yu Fei
Neurosurgery
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Can neuroblastoma be treated?

Neuroblastoma is the most common tumor in childhood, and it is also the most common in infants and toddlers. Typically, neuroblastoma is a type of neuroendocrine tumor, clinically found often in the adrenal glands or in nervous tissues such as the neck, chest, and abdomen. Currently, neuroblastoma can be effectively classified according to its level of risk into low-risk, intermediate-risk, or high-risk groups. For patients in the low-risk group, surgical treatment can achieve satisfactory results; for patients in the intermediate-risk or high-risk groups, treatment often involves a combination of methods, yet still may not achieve satisfactory results.

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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.

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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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Early symptoms of neuroblastoma

For patients with neuroblastoma, in the early stages, due to the small size of the tumor, there generally lacks clear clinical signs or symptoms. Most patients experience mild headaches, dizziness, nausea, and vomiting, accompanied by a certain degree of vertigo. However, in most cases, these symptoms can be tolerated. Patients often have episodic attacks, with a persistent worsening condition. Later, as the tumor grows further, it may lead to an exacerbation of existing symptoms such as headaches, dizziness, nausea, and vomiting. Some patients may also experience abnormalities in the sensation of one side of the body, manifested as numbness, pain, and a tingling sensation.