Neuroblastoma examination items

Written by Chen Yu Fei
Neurosurgery
Updated on September 09, 2024
00:00
00:00

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.

Other Voices

doctor image
home-news-image
Written by Gao Yi Shen
Neurosurgery
43sec home-news-image

Is calcification of neuroblastoma good?

In clinical practice, although calcification is a relatively favorable phenomenon, the overall condition of neuroblastoma does not change significantly because of it. Therefore, it is still not a good sign. For neuroblastoma, whether calcification occurs or not, it remains a form of tumor. Only through early surgical treatment can the problem be fundamentally resolved, otherwise, there is a tendency for recurrence and metastasis to occur later on. Moreover, it is important to note that regardless of whether the tumor calcifies, its nature does not change. Only fundamental treatment can bring better hope, so calcification does not lead to very good outcomes.

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

Symptoms of neuroblastoma recurrence

For neuroblastoma, when the tumor recurs, the patient's original symptoms such as headaches, dizziness, nausea, and vomiting will reappear, occurring intermittently and worsening persistently. Most patients will experience significant increased intracranial pressure, and even frequent nausea and vomiting. Additionally, some neuroblastoma patients experience severe vertigo, especially when changing body positions, where the vertigo is particularly pronounced. For such patients, when the above symptoms and signs occur, they should go to a local hospital as soon as possible for a reassessment using cranial MRI to monitor changes in their condition.

doctor image
home-news-image
Written by Chen Yu Fei
Neurosurgery
33sec home-news-image

Causes of Neuroblastoma

Currently, there is no definitive conclusion about the specific causes of neuroblastoma, but most scholars believe that the occurrence of neuroblastoma is the result of congenital genetic factors combined with acquired factors. For patients with neuroblastoma, there is often a family history of genetic diseases showing a familial clustering tendency. In addition, poor living environments and habits, including exposure to radioactive contamination or prolonged exposure to electromagnetic radiation, may also contribute to the development of neuroblastoma.

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

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.

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.