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Amenorrhea secondary to a vismodegib-induced blockade of follicle-stimulating hormone-receptor activation

机译:vismodegib诱导的卵泡刺激激素受体激活受阻后继发闭经

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摘要

Objective To report a novel mechanism suggestive of early ovarian failure secondary to the anti-tumor hedgehog-pathway inhibitor vismodegib. Design Case report and literature review. Setting Academic and private dermatology and fertility practices. Patient(s) A 34-year-old nulliparous woman with locally advanced basal cell carcinomas who became amenorrheic while receiving oral therapy with vismodegib. Intervention(s) Physical examination and endocrine evaluation. Main Outcome Measure(s) Elevated follicle-stimulating hormone (FSH) and low estrogen in the setting of a normal anti-Müllerian hormone. Result(s) FSH was elevated; estrogen was low. Preantral follicles were detected and anti-Müllerian hormone activity was normal. Menses resumed 5 weeks after cessation of therapy. Conclusion(s) Vismodegib, a first-in-class inhibitor of the hedgehog signaling pathway is indicated for advanced basal cell carcinoma and is associated with amenorrhea. The mechanism is unknown; it has some features of ovarian failure but preserves ovarian potential through blockading of FSH-receptor-dependent signal transduction. This effect appears to be rapidly reversible upon cessation of therapy. Vismodegib and related compounds may have potential for a role in intervention for gynecologic and endocrine disorders and in therapy for other issues involving FSH-dependent function.
机译:目的报道一种新的机制,提示抗肿瘤的刺猬通路抑制剂vismodegib继发于早期卵巢衰竭。设计案例报告和文献审查。制定学术和私人皮肤病学与生育习惯。患者(s)一名34岁的未产妇,患有局部晚期基底细胞癌,在接受vismodegib口服治疗时出现闭经。干预措施身体检查和内分泌评估。主要观察指标在正常的抗苗勒氏激素环境中,促卵泡激素(FSH)升高且雌激素水平降低。结果FSH升高;雌激素低。检测到窦前卵泡,抗苗勒氏管激素活性正常。治疗停止后5周月经恢复。结论Vismodegib是一种刺猬信号通路的一流抑制剂,适用于晚期基底细胞癌,并与闭经有关。机制未知;它具有卵巢衰竭的某些特征,但通过阻断FSH受体依赖性信号转导来保留卵巢潜能。停止治疗后,这种作用似乎可以迅速逆转。 Vismodegib和相关化合物可能在干预妇科和内分泌疾病以及治疗涉及FSH依赖功能的其他问题中具有潜在作用。

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