Gonadoblastoma screening: Difference between revisions
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Created page with "__NOTOC__ {{Gonadoblastoma}} {{CMG}}; {{AE}} ==Overview== There is insufficient evidence to recommend routine screening for [disease/malignancy]. OR According to the [gu..." |
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{{Gonadoblastoma}} | {{Gonadoblastoma}} | ||
{{CMG}}; {{AE}} | {{CMG}}; {{AE}} {{Sahar}} | ||
==Overview== | ==Overview== | ||
There is insufficient evidence to recommend routine screening for gonadoblastoma. However, patients with XY gonadal abnormalities should be followed using sonography starting at age 2, every six months, until gonad can be removed. | |||
There is insufficient evidence to recommend routine screening for | |||
==Screening== | ==Screening== | ||
There is insufficient evidence to recommend routine screening for | *There is insufficient evidence to recommend routine screening for gonadoblastoma. However, patients with XY gonadal abnormalities should be followed using sonography starting at age 2, every six months, until gonad can be removed. <ref name="urlYen & Jaffes Reproductive Endocrinology | ScienceDirect">{{cite web |url=https://www.sciencedirect.com/book/9781455727582/yen-and-jaffes-reproductive-endocrinology |title=Yen & Jaffe's Reproductive Endocrinology | ScienceDirect |format= |work= |accessdate=}}</ref><ref name="pmid10226831">{{cite journal |vauthors=Hatano T, Yoshino Y, Kawashima Y, Shirai H, Iizuka N, Miyazawa Y, Sakata A, Onishi T |title=Case of gonadoblastoma in a 9-year-old boy without physical abnormalities |journal=Int. J. Urol. |volume=6 |issue=3 |pages=164–6 |date=March 1999 |pmid=10226831 |doi= |url=}}</ref> | ||
*Although very uncommon, gonadoblastoma can develop in phenotypically and genotypically normal individuals. In these individuals, the affected gonads must be removed due to the risk of gonadoblastoma conversion to dysgerminoma. Close monitoring with imaging studies also recommended for the contralateral gonads if it is preserved. | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 18:11, 13 February 2019
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Gonadoblastoma Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Gonadoblastoma screening On the Web |
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American Roentgen Ray Society Images of Gonadoblastoma screening |
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Risk calculators and risk factors for Gonadoblastoma screening |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[2]
Overview
There is insufficient evidence to recommend routine screening for gonadoblastoma. However, patients with XY gonadal abnormalities should be followed using sonography starting at age 2, every six months, until gonad can be removed.
Screening
- There is insufficient evidence to recommend routine screening for gonadoblastoma. However, patients with XY gonadal abnormalities should be followed using sonography starting at age 2, every six months, until gonad can be removed. [1][2]
- Although very uncommon, gonadoblastoma can develop in phenotypically and genotypically normal individuals. In these individuals, the affected gonads must be removed due to the risk of gonadoblastoma conversion to dysgerminoma. Close monitoring with imaging studies also recommended for the contralateral gonads if it is preserved.
References
- ↑ "Yen & Jaffe's Reproductive Endocrinology | ScienceDirect".
- ↑ Hatano T, Yoshino Y, Kawashima Y, Shirai H, Iizuka N, Miyazawa Y, Sakata A, Onishi T (March 1999). "Case of gonadoblastoma in a 9-year-old boy without physical abnormalities". Int. J. Urol. 6 (3): 164–6. PMID 10226831.