File:Histopathology of androgen insensitivity.jpg
Histopathology_of_androgen_insensitivity.jpg (364 × 273 pixels, file size: 50 KB, MIME type: image/jpeg)
Summary[edit]
| Description |
Histopathology of testicular tissue showing immature germ cells and spermatagonia with decreased tubular diameter. Scattered groups of Leydig cells appearing immature. |
|---|---|
| Source |
Nichols JL, Bieber EJ, Gell JS. Case of sisters with complete androgen insensitivity syndrome and discordant Müllerian remnants. Fertil Steril. 2009;91:932e15-e18. |
| Article | |
| Portion used |
Single image from an article in a medical journal. |
| Low resolution? |
Resolution of this image will not affect journal subscriptions (i.e. revenue). |
| Purpose of use |
This image illustrates the effects of androgen insensitivity on the cellular level. Individuals with PAIS are at a 50% germ cell malignancy risk because of these abnormalities, and must undergo surgical intervention (i.e. gonadectomy) to prevent metastatic cancer. |
| Replaceable? |
AIS is a very rare disorder, affecting approximately 1 in 100,000 births. Images of this kind (histopathology illustrated by slide of testicular cells) from this population are not likely to exist outside of the medical literature, and thus the image is unlikely to be replaced by one from a free source. |
| Other information |
A source that describes the incidence of germ cell malignancy among individuals with PAIS is Hughes IA, Houk C, Ahmed SF, Lee PA, LWPES Consensus Group, ESPE Consensus Gruop. Consensus statement on management of intersex disorders. Arch Dis Child. 2006;91:554-63. Sources that describe PAIS and its rarity include: (1:) Quigley CA, De Bellis A, Marschke KB, El-Awady MK, Wilson EM, French FS. Androgen receptor defects: historical, clinical, and molecular perspectives. Endocr Rev. 1995;16:271–321. (2:)Mazen I, El-Ruby M, Kamal R, El-Nekhely I, El-Ghandour M, Tantawy S, El-Gammal M. Screening of Genital Anomalies in Newborns and Infants in Two Egyptian Governorates. Horm Res Paediatr. 2010;73:438-442. |
| Fair useFair use of copyrighted material in the context of Androgen insensitivity syndrome//en.wikipedia.org/wiki/File:Histopathology_of_androgen_insensitivity.jpgtrue | |
| Description |
Histopathology of testicular tissue showing immature germ cells and spermatagonia with decreased tubular diameter. Scattered groups of Leydig cells appearing immature. |
|---|---|
| Source |
Nichols JL, Bieber EJ, Gell JS. Case of sisters with complete androgen insensitivity syndrome and discordant Müllerian remnants. Fertil Steril. 2009;91:932e15-e18. |
| Article | |
| Portion used |
Single image from an article in a medical journal. |
| Low resolution? |
Resolution of this image will not affect journal subscriptions (i.e. revenue). |
| Purpose of use |
This image illustrates the effects of androgen insensitivity on the cellular level. Individuals with PAIS are at a 50% germ cell malignancy risk because of these abnormalities, and must undergo surgical intervention (i.e. gonadectomy) to prevent metastatic cancer. |
| Replaceable? |
MAIS is a very rare disorder, affecting fewer than 1 in 100,000 births. Images of this kind (histopathology illustrated by slide of testicular cells) from this population are not likely to exist outside of the medical literature, and thus the image is unlikely to be replaced by one from a free source. |
| Other information |
A source that describes the incidence of germ cell malignancy among individuals with PAIS is Hughes IA, Houk C, Ahmed SF, Lee PA, LWPES Consensus Group, ESPE Consensus Gruop. Consensus statement on management of intersex disorders. Arch Dis Child. 2006;91:554-63. Sources that describe PAIS and its rarity include: (1:) Quigley CA, De Bellis A, Marschke KB, El-Awady MK, Wilson EM, French FS. Androgen receptor defects: historical, clinical, and molecular perspectives. Endocr Rev. 1995;16:271–321. (2:)Mazen I, El-Ruby M, Kamal R, El-Nekhely I, El-Ghandour M, Tantawy S, El-Gammal M. Screening of Genital Anomalies in Newborns and Infants in Two Egyptian Governorates. Horm Res Paediatr. 2010;73:438-442. |
| Fair useFair use of copyrighted material in the context of Mild androgen insensitivity syndrome//en.wikipedia.org/wiki/File:Histopathology_of_androgen_insensitivity.jpgtrue | |
| Description |
Histopathology of testicular tissue showing immature germ cells and spermatagonia with decreased tubular diameter. Scattered groups of Leydig cells appearing immature. |
|---|---|
| Source |
Nichols JL, Bieber EJ, Gell JS. Case of sisters with complete androgen insensitivity syndrome and discordant Müllerian remnants. Fertil Steril. 2009;91:932e15-e18. |
| Article | |
| Portion used |
Single image from an article in a medical journal. |
| Low resolution? |
Resolution of this image will not affect journal subscriptions (i.e. revenue). |
| Purpose of use |
This image illustrates the effects of androgen insensitivity on the cellular level. Individuals with PAIS are at a 50% germ cell malignancy risk because of these abnormalities, and must undergo surgical intervention (i.e. gonadectomy) to prevent metastatic cancer. |
| Replaceable? |
PAIS is a very rare disorder, affecting approximately 1 in 100,000 births. Images of this kind (histopathology illustrated by slide of testicular cells) from this population are not likely to exist outside of the medical literature, and thus the image is unlikely to be replaced by one from a free source. |
| Other information |
A source that describes the incidence of germ cell malignancy among individuals with PAIS is Hughes IA, Houk C, Ahmed SF, Lee PA, LWPES Consensus Group, ESPE Consensus Gruop. Consensus statement on management of intersex disorders. Arch Dis Child. 2006;91:554-63. Sources that describe PAIS and its rarity include: (1:) Quigley CA, De Bellis A, Marschke KB, El-Awady MK, Wilson EM, French FS. Androgen receptor defects: historical, clinical, and molecular perspectives. Endocr Rev. 1995;16:271–321. (2:)Mazen I, El-Ruby M, Kamal R, El-Nekhely I, El-Ghandour M, Tantawy S, El-Gammal M. Screening of Genital Anomalies in Newborns and Infants in Two Egyptian Governorates. Horm Res Paediatr. 2010;73:438-442. |
| Fair useFair use of copyrighted material in the context of Partial androgen insensitivity syndrome//en.wikipedia.org/wiki/File:Histopathology_of_androgen_insensitivity.jpgtrue | |
| Description |
Histopathology of testicular tissue showing immature germ cells and spermatagonia with decreased tubular diameter. Scattered groups of Leydig cells appearing immature. |
|---|---|
| Source |
Nichols JL, Bieber EJ, Gell JS. Case of sisters with complete androgen insensitivity syndrome and discordant Müllerian remnants. Fertil Steril. 2009;91:932e15-e18. |
| Article | |
| Portion used |
Single image from an article in a medical journal. |
| Low resolution? |
Resolution of this image will not affect journal subscriptions (i.e. revenue). |
| Purpose of use |
This image illustrates the effects of androgen insensitivity on the cellular level. Individuals with PAIS are at a 50% germ cell malignancy risk because of these abnormalities, and must undergo surgical intervention (i.e. gonadectomy) to prevent metastatic cancer. |
| Replaceable? |
CAIS is a very rare disorder, affecting approximately 1 in 20,000 births. Images of this kind (histopathology illustrated by slide of testicular cells) from this population are not likely to exist outside of the medical literature, and thus the image is unlikely to be replaced by one from a free source. |
| Other information |
A source that describes the incidence of germ cell malignancy among individuals with PAIS is Hughes IA, Houk C, Ahmed SF, Lee PA, LWPES Consensus Group, ESPE Consensus Gruop. Consensus statement on management of intersex disorders. Arch Dis Child. 2006;91:554-63. Sources that describe PAIS and its rarity include: (1:) Quigley CA, De Bellis A, Marschke KB, El-Awady MK, Wilson EM, French FS. Androgen receptor defects: historical, clinical, and molecular perspectives. Endocr Rev. 1995;16:271–321. (2:)Mazen I, El-Ruby M, Kamal R, El-Nekhely I, El-Ghandour M, Tantawy S, El-Gammal M. Screening of Genital Anomalies in Newborns and Infants in Two Egyptian Governorates. Horm Res Paediatr. 2010;73:438-442. |
| Fair useFair use of copyrighted material in the context of Complete androgen insensitivity syndrome//en.wikipedia.org/wiki/File:Histopathology_of_androgen_insensitivity.jpgtrue | |
Licensing[edit]
 | This image is a scan of a newspaper page or article, and the copyright for it is most likely held by either the publisher of the newspaper or the individual contributors who worked on the articles or images depicted. It is believed that the use of low-resolution images of newspaper pages
qualifies as fair use under the copyright law of the United States. Any other uses of this image, on Wikipedia or elsewhere, may be copyright infringement. See Wikipedia:Non-free content for more information. Note: If the image depicts a person or persons on the cover, it is not acceptable to use the image in the article of the person or persons depicted on the cover, unless used to directly illustrate a point about the publication of the image. Use of the image merely to depict a person or persons in the image will be removed. |
File history
Click on a date/time to view the file as it appeared at that time.
| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 06:34, 29 November 2017 | | 364 × 273 (50 KB) | Theo's Little Bot (talk | contribs) | Reduce size of non-free image (BOT - disable) |
| 23:10, 19 September 2010 | No thumbnail | 438 × 329 (208 KB) | Jonathan.Marcus (talk | contribs) | {{Non-free use rationale |Article = Androgen insensitivity syndrome |Description = Histopathology of testicular tissue showing immature germ cells and spermatagonia with decreased tubular diameter. Scattered groups of Leydig cells appea |
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