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  • 曲 人保, 線崎 敦哉, 山際 健司, 田中 智之, 新家 俊明
    日本泌尿器科学会雑誌
    1991年 82 巻 12 号 1959-1963
    発行日: 1991/12/20
    公開日: 2010/07/23
    ジャーナル フリー
    症例は15歳, 戸籍上男性. 女性化乳房を主訴に当科を紹介された. 血中 testosterone 1.6ng/mlと低値を示し, prolactin 23ng/ml と高値を示した. 血液型ではA型血球とB型血球の混在が見られ, 末梢血リンパ球による染色体分析では46, XX/46, XYのモザイクを示した. 精査中, 右陰嚢内容の腫大と疼痛を訴え, 救急受診した. 手術所見: 右陰嚢内には多量の血性貯留液がみられ, 陰嚢底部に単角子宮, 卵管および卵管釆を認め, さらに陰嚢上部には一部に出血と亀裂を伴う拇指頭大の性腺を認めた. 左陰嚢内には上極部に硬結を伴った性腺を認めた. 組織学的所見では右性腺は卵巣, 左性腺は精巣で硬結部は卵巣組織であった. 右性腺内には詳細な検索によっても精巣組織は確認できなかったが, 同側に精管が認められた. 以上の所見より本症例は, 右側に単角子宮ヘルニアを伴う卵巣と, 左側に卵精巣を認める46, XX/46, XYキメラ真性
    半陰陽
    と診断された. 右側卵巣の陰嚢内への下降と右精管の発生は胎生期に左側精巣より分泌された testosterone が関与したものと考えられた.
  • 安岡 利恵, 宮垣 拓也, 北尾 善孝, 門谷 洋一, 中村 隆一
    日本臨床外科学会雑誌
    2004年 65 巻 8 号 2210-2215
    発行日: 2004/08/25
    公開日: 2009/03/31
    ジャーナル フリー
    混合型性腺異常発生症では,染色体異常が主に45X/46XYなどのmosaicであるために,一側性腺が精巣で他側が線状性腺を持ち,未分化な膣,子宮,卵管などMüller管の遺残を認めることがある.また,混合型性腺異常発生症は様々な身体学的特徴を有する.本症は主に小児科医,小児外科医が関わる疾患であるが,今回われわれは45歳にして成人鼠径ヘルニア治療時に偶然混合型性腺異常発生症を発見し,十分なインフォームドコンセントのもと,線状性腺とMüller管遺残を摘出した興味深い症例を経験したので,これを報告する.
  • 三宅 宗悦
    人類學雜誌
    1937年 52 巻 7 号 225-258
    発行日: 1937/07/15
    公開日: 2008/02/26
    ジャーナル フリー
  • 田中 義雄
    順天堂医学
    1895年 M28 巻 194 号 78-81
    発行日: 1895/01/31
    公開日: 2015/06/17
    ジャーナル フリー
  • 森田 敏弘, 鷲見 靖彦, 須原 貴志, 山田 慎, 堅田 昌弘
    日本臨床外科学会雑誌
    1998年 59 巻 10 号 2690-2694
    発行日: 1998/10/25
    公開日: 2009/01/22
    ジャーナル フリー
    男性
    半陰陽
    における鼠径部子宮ヘルニアは稀で,本邦では54例の報告をみるにすぎない.今回われわれは52歳の男性に鼠径部子宮ヘルニアを認めた症例を経験したので報告する.患者は鼠径部から陰嚢に及ぶ有痛性腫瘤を主訴に来院した.腹部CT, MRIにて鼠径部から陰嚢に及ぶ腫瘤陰影と腸管ガス像を認めた.腸管の鼠径ヘルニア嵌頓と診断し,手術を施行した.ヘルニア嚢内にはS状結腸が嵌頓しており,ヘルニア根治術を施行した.右鼠径管内にはさらに, 2個の卵巣・卵管様構造物と子宮様構造物が認められた.病理組織学的に卵巣様構造物は精巣であり,子宮様構造物は子宮であった.患者の染色体,ホルモン学的検査は正常であった.
  • 有馬 七五郎
    應用獸醫學雑誌
    1943年 16 巻 7 号 425-426_1
    発行日: 1943/07/20
    公開日: 2008/10/24
    ジャーナル フリー
  • 菊池 滋
    應用獸醫學雑誌
    1940年 13 巻 11 号 746-753_1
    発行日: 1940/11/20
    公開日: 2008/10/24
    ジャーナル フリー
  • 森 義則, 水谷 修太郎
    日本泌尿器科學會雑誌
    1968年 59 巻 10 号 857-864
    発行日: 1968/10/20
    公開日: 2010/07/23
    ジャーナル フリー
    Two cases of true hermaphroditism were experienced in two-year- and three-year-old siblings. Exploratory laparotomy and histological examination revealed that each sibling had ovary on the left side and ovotestis on the right side and that each had a fallopian tube on the ovarian side and maldeveloped spermatic cord on the ovotesticular side. They were both sex chromatin positive and their sex chromosomes consisted of XX. Their external genitalia were quite similar to each other.
  • 浦野 悦郎
    日本泌尿器科學會雑誌
    1960年 51 巻 1 号 78-97
    発行日: 1960年
    公開日: 2010/07/23
    ジャーナル フリー
  • 石田 肇
    日本泌尿器科學會雑誌
    1979年 70 巻 6 号 655-667
    発行日: 1979年
    公開日: 2010/07/23
    ジャーナル フリー
    Pituitary-gonadal endocrine function was studied by measuring serum LH, FSH and testosterone (T) levels under various conditions using radioimmunoassay methods in 18 patients with various types of male hermaphroditism. Among them, 11 patients were classified as group A1 (;male hermaphroditism with no breast development and rudimentary or no mullerian structures), 3 patients as group A2 (;male hermaphroditism with well formed mullerian structures) and 2 patients as group B2 (;male hermaphroditism with breast development and ambiguous external genitalia) according to the classification modified from that proposed by Jones. In the other 2 patients, it was not determined whether they belonged to group A1 or group B2 because of their prepubertal age.
    In addition, 4 patients with true hermaphroditism and 3 patients with gonadal dysgenesis were studied for comparison. The pubertal and postpubertal patients with male hermaphroditism excluding those of group B2 showed strikingly elevated levels of both serum LH and FSH. The levels of serum LH and FSH were further elevated by LH-RH administration. Serum T levels in them were widely ranged from subnormal to normal adult male levels, and hCG stimulation test revealed a poor Leydig cell reserve capacity in some cases.
    In the pubertal and postpubertal patients with male hermaphroditism of group B2, serum FSH values were in the upper limit of normal adult male range, but the levels of serum LH were abnormally elevated despite their normal or high levels of serum T. Serum gonadotropin levels in two patients with male hermaphroditism of group A2 were studied along with usual course of clinical treatment. It was observed that further increased levels of serum gonadotropins after castration were suppressed to almost undetectable levels by estrogen replacement therapy. The serum gonadotropin levels in one of the patients with male hermaphroditism of group B2 were not suppressed by single administration of testosterone depot 100mg.
    In contrast to these abnormally elevated levels of serum gonadotropins in adult patients with male hermaphroditism, the prepubertal cases showed normal age-matched male levels of serum gonadotropins.
    Four patients were studied longitudinally for 3 or 5 years and abrupt rises of serum gonadotropin levels to the abnormally high range were observed with the onset of puberty. These pubertal rises of serum gonadotropin levels from the normal range to an abnormally high range were also observed in the studies on patients with true hermaphroditism.
    Meanwhile, the patients with gonadal dysgenesis of prepubertal age showed somewhat elevated levels of serum gonadotropins. It is concluded that development of puberty causes abnormal changes in pituitary gonadal endocrine function in patients with male hermaphroditism. The aspects of these abnormalities are thought to be compatible in some cases with those of primary gonadal failure and in some cases with those of androgen insensitivity in target organs.
    Possible mechanism was discussed for these abnormal alterations in pituitary gonadal endocrine axis during puberty in patients with male hermaphroditism.
  • 森田 迪夫, 天野 武, 北川 久
    日本獣医師会雑誌
    1966年 19 巻 3 号 119-122
    発行日: 1966/03/20
    公開日: 2011/06/17
    ジャーナル フリー
    Two cases, A and B, of hermaphroditism were found among Landrace swine kept at the prefectural experiment stations of Kagawa and Okayama, respectively. Case A was the testicular type of hermaphroditism and case B the bi-gonadal type.
    The testis, with no scrotum, was relatively well developed in both cases. The ovary was present restrictedly on one side of the testis in case A. The uterus was almost as large as the normal one in case A, with yellow turbid fluid in its cavity. It was hardly developed in case B. The oviduct was not formed on the right side of case A, where the uterine horn became a blind end. It was present on the left side of case A and both sides of case B, running along the epididymis.
    The ductus deferens took a remarkably winding course near the site where the uterine horn was attached to the ligamentum latum uteri. It ran parallel to that on the opposite side and opened at a site close to the orifice of the urethra. The prostate was observed in the submucocal tissue of the vagina in case A under the microscope. There was neither seminal vesicle nor bulbourethral gland.
    Histological examination revealed marked hyperplasia of interstitial cells, hypoplasia and adipose degeneration of epithelial cells of the seminiferous tubules in both cases. There were necrotic foci surrounded by a thick layer of granulation tissue in the testis, acute catarrhal endometritis, diffuse cellular infiltration of the prostate and formation of lymph follicles in case A. Hypoplasia and necrosis were noticed in the granular layer of the ovary in case B.
  • 田中 義雄
    順天堂医学
    1896年 M29 巻 238 号 1070-1072
    発行日: 1896/11/30
    公開日: 2015/06/17
    ジャーナル フリー
  • 小川
    應用獸醫學雑誌
    1932年 5 巻 10 号 816
    発行日: 1932/10/20
    公開日: 2008/10/24
    ジャーナル フリー
  • 落合 京一郎
    日本先天異常学会会報
    1964年 4 巻 2 号 56-58
    発行日: 1964/10/30
    公開日: 2019/02/01
    ジャーナル フリー
  • 松崎 茂, 牧野 駿一, 伊東 充宏, 内田 広夫, 野首 光弘, 松本 清一
    日本小児外科学会雑誌
    1995年 31 巻 5 号 809-813
    発行日: 1995/08/20
    公開日: 2017/01/01
    ジャーナル フリー
    不完全型精巣性女性化症候群を呈した男性仮性
    半陰陽
    の1例を経験した.主訴は,学童期になり気付かれた陰核肥大と鼠径部腫瘤であった.染色体は46, XY であった.内分泌検査では testosterone(T)と FSH が高値であった. dihydrotestosterone(DHT) はやや低値であった. T:DHT 比は22であった. hCG 負荷での反応は T, DHT 共に良好であり,T:DHT 比は17となった.女児として養育する方針とし手術を施行した.鼠径部腫瘤は精巣であり.これに連なる精巣上体と輸巣管も存在した、精巣,精巣上体,輸巣管を切除した、腹腔内検索では Muller 管由来の臓器や卵巣は存在しなかった.陰核には subtunical total reduction clitoroplasty を施行した、摘出精巣の病理学的検索では,精子形成細胞は存在せず, Sertoli 細胞と Leydig 細胞の増加がみられた.術後はホルモン補充療法を行なっている.
  • 性染色体構成と性腺および導管系の分化
    大島 博幸, 酒井 邦彦, 高木 健太郎, 池上 茂
    日本泌尿器科學會雑誌
    1974年 65 巻 11 号 732-740
    発行日: 1974/11/20
    公開日: 2010/07/23
    ジャーナル フリー
    Eleven cases of true hermaphrodites were investigated with special reference to the relationship between differentiation of gonads and development of sexual duct systems. On most of them were performed studies of the sex chromatin, fluorescent body and chromosomal analysis. Also, reported cases in Japan as well as in foreign countries were collected and reviewed.
    Chromosomal analysis on 9 cases revealed chromosomal constitutions of 46, XX in 3 cases, 46, XY in 4 and 46, XX/46, XY in 2.
    Four cases out of 5 patients with a testis at one side and an ovary at the opposite showed Y-bearing chromosomal constitutions. Most of reported cases with a similar type of gonadal developement as the above mentioned were proved to have Y chromosome in their stem cells.
    Analysis of chromosomes in myelocytes and lymphocytes from a patient with 46, XX/46, XY revealed an interesting result. Twenty-one myelocytes out of 24 had chromosomal constitution of 46, XY and only 3 had 46, XX, whereas almost all of lymphocytes investigated after culture of peripheral blood had 46, XX constitution. It may be suggested from the above finding that cell populations are different from one tissue to another and may influence the differentiation of the primordial gonad toward a testis or ovary. It was another interesting finding that the fluorescent body was observed in 19% of lymphocytes from the patient mentioned above. The observation indicates the importance of examining Barr body as well as fluorescent body on more than two kinds of tissues, because native cells without cell-culture can be utilized for the examinations.
    Six true hermaphrodites investigated for both Barr and fluorescent bodies consisted of two of 46, XX, 46, XY and 46, XX/46, XY, respectively. Both bodies were positive in each case with mosaicism 46, XX/ 46, XY, although their frequencies were at lower percentage than normal female or male. On the other hand, only a few Barr or fluorescent bodies were recognized in each case of 46, XY or 46, XX, respectively. It is difficult to decide whether the above results were caused by an unrecognized mosaicism or not.
    From the observations of true hermaphrodites and XX-males, there has been raised an assumption that a sex-determining factor may locate on one of autosomes to which Y chromosome may affect as a regulating factor. This assumption, however, appears not sufficient to explain the differentiation of the ovarian tissue in the case of 46, XY.
    Testes in the foetus stimulate the differentiation and development of the Wolflian duct and suppress the Mullerian duct. The former function appears to be controlled by one of androgens secreted from the foetal testis. From the observation of clinical cases and animal experiments, the latter function seems to be closely related to the chromosomal constitution of cells composing the ductal tissue, while this function must be mediated by a chemical messenger produced from the foetal testis.
  • 七野 滋彦, 佐藤 太一郎, 浄土 魏, 神谷 武
    日本臨床外科医学会雑誌
    1964年 25 巻 3 号 224-228
    発行日: 1964/05/25
    公開日: 2009/03/31
    ジャーナル フリー
  • 高井 修道, 島村 昭吾, 疋田 政博
    日本泌尿器科學會雑誌
    1967年 58 巻 3 号 331-336
    発行日: 1967年
    公開日: 2010/07/23
    ジャーナル フリー
    A 12-year-old patient with ambiguous external genitalia was reported. The social sex of the patient was male. The external genitalia showed scrotal hypospadia with bifid scrotum and no left scrotal content. The urinary excretion of gonadotropin, 17-KS, 17-OHCS, estrogen, pregnanediol and pregnanetriol were under 8muu/day, 3.3-5.0mg/day, 1.3-2.1mg/day, 5.0-9.0μg/day, 0.90-1.18mg/day and 0.2-0.22mg/day, respectively. At laparotomy no left testis was found in retroperitoneal cavity from inguinal ring up to renal hilum region. At the region of lateral wall of pelvic cavity a small ovary-like body, measuring 2.0×1.0×0.6cm, fimbria and oviduct were found. At the middle point of retrovesical region the left oviduct fused with right seminal duct, making a small bicornate uterus which ended blindly at the perineal region. Histological examination of left gonad revealed an ovary with occasional primitive follicles and that of right gonad revealed relatively well developed testis. Chromosome examination showed a karyotype of 46/XY. From the results above mentioned it was notd that the diagnosis of this patient was a tune hermaphroditism with a karyotype of 46/XY.
  • 野村 紘一
    日本獣医師会雑誌
    1986年 39 巻 8 号 520-524
    発行日: 1986/08/20
    公開日: 2011/06/17
    ジャーナル フリー
    患犬は2年7カ月齢の四国犬で, 血統的には祖父母が同腹子であり, 本例との同腹子のなかにもう1頭の
    半陰陽
    犬が存在したという. 本犬の外陰部には陰嚢様陰唇と発育不全の陰茎骨を入れた肥大陰核を備えていた. 膣の発達はやや悪く, 陰裂も狭小であった. 内部生殖器は精巣, 精巣上体, 蔓状静脈叢, 輸精管, 精巣導帯ならびに子宮と膣から構成され, 両性が混在しているものの, 雄性が優勢であった. したがって, 本犬は形態学的には雄性傾向のきわめて強い雄性仮性
    半陰陽
    と診断された.
    いっぽう, 本犬の末梢血中白血球による染色体分析の結果, 染色体 (2n) の数は78, 性染色体はXX型を示し, さらに, 口腔粘膜上皮の性染色質検査の結果も雌型を示していた.
    このように, 本犬は表現形が雄性化の強い雄性仮性
    半陰陽
    であるにもかかわらず, 性染色体構成はXX型を示しているところから, 雄性決定因子を活性化したのはY染色体以外の要素であり, 発育不全の精巣から十分なミラー管抑制因子が産生されなかったか, あるいはミラー管のこれらに対する感受性が著しく低下していたことが想像される.
  • 成富 研二, 池田 琢哉, 八木 俊一, 角田 和之, 後藤 俊弘
    日本先天異常学会会報
    1977年 17 巻 3 号 413-414
    発行日: 1977/09/30
    公開日: 2019/02/01
    ジャーナル フリー
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