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A tortuous proximal urethra in urorectal septum malformation sequence?

机译:尿道隔中畸形的曲折性近端尿道?

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We observed a newborn boy with urorectal septum malformation sequence. Anomalies of the genitalia and rectum were present. He expired on the first day of life, due to severe lung hypoplasia. Autopsy showed a colon that ended in a blind sac, an enlarged bladder with no grossly visible urethra, and dysplastic kidneys. A cone-shaped tissue at the usual site of the bladder outlet contained tortuous and slit-like lumina, suggesting an undeveloped proximal urethra. The urethral structure was lined by transitional epithelium with squamous metaplasia. Many small buds-lined with columnar epithelium-branched from the urethral structure. These ductal buds lined with columnar epithelium stained for prostatic acid phosphatase. Basal cells surrounding the ductal buds stained for p63 and high molecular weight cytokeratin-supporting an interpretation that the buds were early prostatic ducts with normal histology. To our knowledge, these are the first histological images of an undeveloped, obstructed urethra associated with the urorectal septum malformation sequence.
机译:我们观察到一个新生男孩,其尿道隔间隔畸形序列。存在生殖器和直肠异常。由于严重的肺发育不良,他在生命的第一天就死了。尸检显示结肠末端为盲囊,膀胱肿大,无明显尿道,肾脏发育不良。膀胱出口通常部位的圆锥形组织包含曲折的狭缝状腔腔,提示尿道近端未发育。尿道结构衬有鳞状化生的过渡上皮。许多小芽排成柱状上皮,从尿道结构分支。这些导管芽内衬有柱状上皮,并被前列腺酸性磷酸酶染色。导管芽周围的基底细胞染色为p63和高分子量细胞角蛋白,这支持了芽是具有正常组织学的早期前列腺导管的解释。据我们所知,这是与尿直肠中隔畸形序列相关的未发育,阻塞性尿道的第一批组织学图像。

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