Gonadoblastoma natural history, complications and prognosis: Difference between revisions
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Latest revision as of 21:54, 29 July 2020
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Gonadoblastoma Microchapters |
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Treatment |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[2]
Overview
Gonadoblastoma per se is a benign tumor, however, it has the capacity to convert to dysgerminoma or other more malignant germ cell tumors and produce steroids with resultant virilization. Prognosis is generally excellent after removing the tumor.
Natural History, Complications, and Prognosis
Natural History
- Gonadoblastoma usually develops in the first and second decades of life.[1]
- If complicated by an invasive germ cell tumor, then prognosis depends on the staging of the tumor.[2]
- It is usually diagnosed during a workup for sex organ developmental disorders, primary amenorrhea, and/or virilization.
Complications
- Common complications of gonadoblastoma include:[1]
- Dysgerminoma
- Seminoma
- Other gonadal malignancies
Prognosis
- Prognosis is generally excellent if the tumor is diagnosed and removed early.[3]
- Depending on the presence of the coexisting germinal tumors at the time of diagnosis, the prognosis may vary.
References
- ↑ 1.0 1.1 Sperling, M (2014). Pediatric endocrinology. Philadelphia, PA: Elsevier/Saunders. ISBN 978-1-4557-4858-7.
- ↑ Saia, Philip (2018). Clinical gynecologic oncology. Philadelphia, PA: Elsevier. ISBN 978-0-323-40067-1.
- ↑ "Pediatric Endocrinology | ScienceDirect".