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淋巴细胞核型分析在条索状性腺原发性闭经中的诊断价值有限。

Limited diagnostic value of lymphocytic karyotype in primary amenorrhea with streak gonads.

作者信息

Surico N, Messina M, Ponzio G, Libanori E, Chiodo F, Milani P, Folpini E

机构信息

Istituto di Ginecologia e Ostetricia dell'Università di Torino, Turin, Italy.

出版信息

Eur J Obstet Gynecol Reprod Biol. 1987 Oct;26(2):145-50. doi: 10.1016/0028-2243(87)90049-9.

Abstract

Cytogenetic data represent a first line diagnostic aid in gonadal dysgenesis. Generally, the results of a peripheral blood examination reflect the genotypic alteration of the patient. Nevertheless, on occasion one may encounter cases in which clinical and hormonal evidence suggestive of dysgenesis is not accompanied by an anomalous chromosomal finding, upon cytogenetic analysis of the peripheral blood. In these cases, a cytogenetic alteration may be present in cellular components of the ovary and the cutis. In the light of the above, two patients presenting with primary hypergonadotropic amenorrhea, streak gonads and normal peripheral karyotype are described. In one patient presenting with phenotype alterations, ovarian wedge biopsy via laparotomy followed by cytogenetic analysis of ovarian tissue and tissue from the cutis revealed a 45,X/46,XX-type mosaicism. In the other patient, the ovarian cytogenetic findings were unremarkable. Extending chromosomal analysis to several tissues, beyond the peripheral level, in selected cases, is discussed.

摘要

细胞遗传学数据是性腺发育不全一线诊断的辅助手段。一般来说,外周血检查结果反映了患者的基因型改变。然而,有时在外周血细胞遗传学分析中,可能会遇到临床和激素证据提示发育不全但染色体检查结果正常的病例。在这些病例中,卵巢和皮肤的细胞成分中可能存在细胞遗传学改变。鉴于上述情况,本文描述了两名表现为原发性高促性腺激素性闭经、条索状性腺且外周核型正常的患者。其中一名有表型改变的患者,经剖腹手术进行卵巢楔形活检,随后对卵巢组织和皮肤组织进行细胞遗传学分析,发现了45,X/46,XX型嵌合体。另一名患者的卵巢细胞遗传学检查结果无异常。本文讨论了在特定病例中,除外周血外,将染色体分析扩展到多个组织的情况。

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Hormonal and cytogenetic studies in phenotypically female patients with gonadal dysgenesis.
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Familial ovarian dysgenesis in 46,XX females.46,XX女性的家族性卵巢发育不全
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