Gonadoblastoma: Difference between revisions
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== Gonadoblastoma == | |||
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Revision as of 01:10, 20 February 2025
Gonadoblastoma is a rare type of tumor that is often associated with gonadal dysgenesis and disorders of sex development. It is most commonly found in individuals with a Y chromosome, including those with Turner syndrome who have a Y chromosome mosaicism.
Etiology
The exact cause of gonadoblastoma is not known. However, it is believed to be related to the presence of the Y chromosome in the cells of the gonads. This is supported by the fact that the majority of cases are found in individuals with a Y chromosome, including those with Turner syndrome who have a Y chromosome mosaicism.
Symptoms
The symptoms of gonadoblastoma can vary depending on the size and location of the tumor. Some individuals may not have any symptoms, while others may experience abdominal pain, a palpable mass, or signs of hormone overproduction such as precocious puberty or virilization.
Diagnosis
The diagnosis of gonadoblastoma is typically made based on the results of imaging studies such as ultrasound, computed tomography (CT) scan, or magnetic resonance imaging (MRI). A biopsy of the tumor may also be performed to confirm the diagnosis.
Treatment
The treatment for gonadoblastoma usually involves surgery to remove the tumor. In some cases, chemotherapy or radiation therapy may also be used. Individuals with a Y chromosome are also typically advised to undergo gonadectomy to prevent the development of gonadoblastoma.
Prognosis
The prognosis for individuals with gonadoblastoma is generally good, especially if the tumor is detected and treated early. However, there is a risk of the tumor developing into a more aggressive type of cancer known as dysgerminoma.
