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一名80岁女性卵巢卵黄囊瘤的非典型表现:病例报告及文献复习

Atypical Presentation of an Ovarian Yolk Sac Tumor in an 80-Year-Old Woman: A Case Report and Review of the Literature.

作者信息

Maldonado Vanessa, Masvidal María, Morente Laguna Vanessa, Cimerman Jacqueline, Martinez Soriano Salvador

机构信息

Institut d'Oncologia de la Catalunya Sud, Hospital Universitari Sant Joan de Reus, Institut d'Investigació Sanitària Pere Virgili (IISPV), Universitat Rovira i Virgili, Tarragona, Spain.

出版信息

Case Rep Oncol. 2024 Dec 3;17(1):1342-1350. doi: 10.1159/000542244. eCollection 2024 Jan-Dec.

Abstract

INTRODUCTION

Ovarian yolk sac tumors after the menopause are very rare.

CASE PRESENTATION

We report an atypical case of yolk sac tumor in an octogenarian woman, who presented to the hospital with anasarca, ascites, toxic syndrome, and an abdominal mass. Serum alpha-fetoprotein (AFP) levels were highly increased (246,720 ng/mL), and malignant cells with positive AFP immunohistochemical expression were detected in a diagnostic paracentesis. The definitive diagnosis was established by histopathological examination of the surgical specimen and immunohistochemical detection of positivity for AFP, glypican 3, cytokeratin AE1/AE3, and focal positivity for SALL4 and CK7. Adjuvant chemotherapy was refused by the patient. Postoperative AFP values decreased to normal limits. One year after surgery, she remains in good clinical condition without evidence of tumor recurrence. In a review of the literature, 11 cases of yolk sac tumors in postmenopausal women were collected. The mean age of the patients was 63.4 years (range 58-82 years). Frequent findings were FIGO stage II, cytoreductive surgery, immunohistochemical analyses of a large panel of markers, postoperative chemotherapy, and no tumor recurrence (except in 1 patient who died), although the length of follow-up was relatively short or unclearly stated.

CONCLUSION

The present case report illustrates that yolk sac tumors in very old women may have a favorable clinical course without signs of recurrence even in the absence of radical surgical resection with curative intent and associated adjuvant chemotherapy.

摘要

引言

绝经后卵巢卵黄囊瘤非常罕见。

病例报告

我们报告一例非典型的卵黄囊瘤,患者为一位八旬女性,因全身水肿、腹水、中毒综合征及腹部肿块入院。血清甲胎蛋白(AFP)水平显著升高(246,720 ng/mL),诊断性腹腔穿刺抽出物中检测到AFP免疫组化表达阳性的恶性细胞。通过手术标本的组织病理学检查以及AFP、磷脂酰肌醇蛋白聚糖3、细胞角蛋白AE1/AE3免疫组化检测阳性,SALL4和CK7局灶阳性确诊。患者拒绝辅助化疗。术后AFP值降至正常范围。术后一年,她临床状况良好,无肿瘤复发迹象。在文献回顾中,收集到11例绝经后女性卵黄囊瘤病例。患者平均年龄63.4岁(范围58 - 82岁)。常见表现为国际妇产科联盟(FIGO)II期、肿瘤细胞减灭术、大量标志物的免疫组化分析、术后化疗且无肿瘤复发(1例死亡患者除外),尽管随访时间相对较短或表述不明确。

结论

本病例报告表明,高龄女性的卵黄囊瘤即使未进行根治性手术切除及相关辅助化疗,也可能有良好的临床病程且无复发迹象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35dd/11614451/862c2f947085/cro-2024-0017-0001-542244_F01.jpg

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