Early symptoms of neuroblastoma

Written by Chen Yu Fei
Neurosurgery
Updated on September 01, 2024
00:00
00:00

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.

Other Voices

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

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.

doctor image
home-news-image
Written by Chen Yu Fei
Neurosurgery
45sec home-news-image

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.

doctor image
home-news-image
Written by Chen Yu Fei
Neurosurgery
44sec home-news-image

How do you get neuroblastoma?

Currently, there is no consensus on the specific causes of neuroblastoma. In most cases, it is believed to be caused by the failure of primitive myeloid epithelial cells to continue differentiating, which is somewhat linked to congenital genetic factors. Additionally, poor lifestyle choices and exposure to certain chemical carcinogens, including long-term exposure to radiation, can potentially lead to neuroblastoma. Neuroblastoma is a highly malignant tumor that generally grows and develops rapidly. It often adheres to surrounding tissues in the early stages of the disease, making complete surgical removal quite difficult, and typically has a poor prognosis.

doctor image
home-news-image
Written by Chen Yu Fei
Neurosurgery
48sec home-news-image

Neuroblastoma examination items

For neuroblastoma, the examination items mainly include the patient's vital signs and physical examination, including detailed examinations to observe if there are any obvious pathological signs. Additionally, it is necessary to inquire about the patient’s medical history, especially past medical history and family history. Main examination items include laboratory tests, routine blood and urine tests, biochemistry, and tumor-related tests. Furthermore, examinations also involve using a cranial CT scan, MRI of the head, and if necessary, an enhanced MRI scan of the head, to further determine the presence of neuroblastoma, as well as its location, quantity, and the relationship between the surrounding tissues, blood vessels, and nerves.

doctor image
home-news-image
Written by Chen Yu Fei
Neurosurgery
44sec home-news-image

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.