A CASE OF MIXED GONADAL DYSGENESIS ACCIDENTALLY DETECTED DURING TREATMENT FOR INGUINAL HERNIA
Mixed gonadal dysgenesis has a chromosomal aberration mainly due to 45X/46XY chromosomal mosaic, so the lateral gonad may be a testis and the contralateral a linear gonad with Müllerian duct rests including an undifferentiated vagina, uterus, and oviduct. Mixed gonadal dysgenesis is also associated...
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Published in | Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association) Vol. 65; no. 8; pp. 2210 - 2215 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Japan Surgical Association
2004
|
Online Access | Get full text |
ISSN | 1345-2843 1882-5133 |
DOI | 10.3919/jjsa.65.2210 |
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Abstract | Mixed gonadal dysgenesis has a chromosomal aberration mainly due to 45X/46XY chromosomal mosaic, so the lateral gonad may be a testis and the contralateral a linear gonad with Müllerian duct rests including an undifferentiated vagina, uterus, and oviduct. Mixed gonadal dysgenesis is also associated with certain physical features. Although it is principally treated by pediatric physicians and surgeons, we found it accidently in a 45-year-old patient being treated for inguinal hernia. After getting sufficiently informed consent, we successfully removed the linear gonad and Müllerian duct. |
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AbstractList | Mixed gonadal dysgenesis has a chromosomal aberration mainly due to 45X/46XY chromosomal mosaic, so the lateral gonad may be a testis and the contralateral a linear gonad with Müllerian duct rests including an undifferentiated vagina, uterus, and oviduct. Mixed gonadal dysgenesis is also associated with certain physical features. Although it is principally treated by pediatric physicians and surgeons, we found it accidently in a 45-year-old patient being treated for inguinal hernia. After getting sufficiently informed consent, we successfully removed the linear gonad and Müllerian duct. |
Author | YASUOKA, Rie KADOTANI, Yoichi MIYAGAKI, Takuya NAKAMURA, Ryuichi KITAO, Yoshitaka |
Author_xml | – sequence: 1 fullname: KITAO, Yoshitaka organization: Department of Surgery, Kyoto Nishijin Hospital – sequence: 1 fullname: NAKAMURA, Ryuichi organization: Department of Surgery, Kyoto Nishijin Hospital – sequence: 1 fullname: MIYAGAKI, Takuya organization: Department of Surgery, Kyoto Nishijin Hospital – sequence: 1 fullname: YASUOKA, Rie organization: Department of Surgery, Akashi City Hospital – sequence: 1 fullname: KADOTANI, Yoichi organization: Department of Surgery, Akashi City Hospital |
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References | 10) Sohval AR: “Mixed” gonadal dysgenesis: A variety of hermoaphroditism. Am J Hum Genet 15: 155-158, 1962 5) Siiteri PK, Wilson JD: Testosterone formation and metabolism during male sexual differentiation in the human embryo. J Clin Endocrinol Metab 38: 113-125, 1974 8) 梅原次男,熊本悦明,丸田 浩 他:尿道下裂及び男性半陰陽におけるvaginal rest (残存膣)の形態学的検討.日泌会誌 76: 635-644, 1985 4) Berta P, Hawkins JR, Sinclair AH, et al: Genetic evidence equating SRY and the testis-determining factor. Nature 348: 448-450, 1990 3) 岩動孝一郎:男性仮性半陰陽.日泌会誌 85: 1189-1212, 1994 11) Mendez JP, Ulloa-Aguirre A, Kofman-Alfaro S, et al: Mixed gonadal dysgenesis: Clinical, cytogenetic, endocrinolo gical, and histopathological findings in 16patients. Amer J Med Genet 46: 263-267, 1993 7) 榊原尚行,野々村克也,小柳知彦 他:尿道下裂の臨床的,内分泌学的検討.日泌会誌 76: 716-722, 1985 13) 鞁嶋有紀,花木啓一,澤田宏志 他: Y染色体成分を含んだ性腺形成不全の2例.小児臨 53: 1623-1626, 2000 2) 島 博基,生駒文彦: Müller管退縮物質について.日泌会誌 84: 1747-1758, 1993 14) 島本良子,大隅 昇,石川 正:仮性半陰陽2例に対する治療経験.形成外科 42: 39-49, 1999 6) 小柳知彦,野々村克也:尿道下裂.日泌会誌 81: 1609-1617, 1990 1) 藤本昌敏:卒後教育シリーズ 第4回 性分化異常の診断と治療.小児診療 50: 164-171, 1987 9) 福谷恵子:男性仮性半陰陽.日臨 55: 120-124, 1997 12) 服部重人,高橋洋子,三宅 浩他: 45, X/46, XY性腺形成不全症の3例.ホルモンと臨 48: 1033-1037, 2000 |
References_xml | – reference: 8) 梅原次男,熊本悦明,丸田 浩 他:尿道下裂及び男性半陰陽におけるvaginal rest (残存膣)の形態学的検討.日泌会誌 76: 635-644, 1985 – reference: 3) 岩動孝一郎:男性仮性半陰陽.日泌会誌 85: 1189-1212, 1994 – reference: 9) 福谷恵子:男性仮性半陰陽.日臨 55: 120-124, 1997 – reference: 5) Siiteri PK, Wilson JD: Testosterone formation and metabolism during male sexual differentiation in the human embryo. J Clin Endocrinol Metab 38: 113-125, 1974 – reference: 6) 小柳知彦,野々村克也:尿道下裂.日泌会誌 81: 1609-1617, 1990 – reference: 1) 藤本昌敏:卒後教育シリーズ 第4回 性分化異常の診断と治療.小児診療 50: 164-171, 1987 – reference: 11) Mendez JP, Ulloa-Aguirre A, Kofman-Alfaro S, et al: Mixed gonadal dysgenesis: Clinical, cytogenetic, endocrinolo gical, and histopathological findings in 16patients. Amer J Med Genet 46: 263-267, 1993 – reference: 12) 服部重人,高橋洋子,三宅 浩他: 45, X/46, XY性腺形成不全症の3例.ホルモンと臨 48: 1033-1037, 2000 – reference: 10) Sohval AR: “Mixed” gonadal dysgenesis: A variety of hermoaphroditism. Am J Hum Genet 15: 155-158, 1962 – reference: 14) 島本良子,大隅 昇,石川 正:仮性半陰陽2例に対する治療経験.形成外科 42: 39-49, 1999 – reference: 2) 島 博基,生駒文彦: Müller管退縮物質について.日泌会誌 84: 1747-1758, 1993 – reference: 7) 榊原尚行,野々村克也,小柳知彦 他:尿道下裂の臨床的,内分泌学的検討.日泌会誌 76: 716-722, 1985 – reference: 13) 鞁嶋有紀,花木啓一,澤田宏志 他: Y染色体成分を含んだ性腺形成不全の2例.小児臨 53: 1623-1626, 2000 – reference: 4) Berta P, Hawkins JR, Sinclair AH, et al: Genetic evidence equating SRY and the testis-determining factor. Nature 348: 448-450, 1990 |
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Title | A CASE OF MIXED GONADAL DYSGENESIS ACCIDENTALLY DETECTED DURING TREATMENT FOR INGUINAL HERNIA |
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