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罕见的源于小的原发性肺腺癌的巨大卵巢转移瘤:一例报告

Rare giant ovarian metastasis arising from a small primary lung adenocarcinoma: a case report.

作者信息

Wang Baofeng, Jia Youjuan, Wang Jiang, Zhang Zhenjiang, Ding Yilin, Lu Hengxiao

机构信息

Department of Thoracic Surgery, The First Affiliated Hospital of Weifang Medical University (Weifang people's Hospital), School of Clinical Medicine, Weifang Medical University, Weifang, China.

Department of Gynecology, The First Affiliated Hospital of Weifang Medical University (Weifang people's Hospital), Weifang, China.

出版信息

Front Surg. 2023 Sep 12;10:1278076. doi: 10.3389/fsurg.2023.1278076. eCollection 2023.

Abstract

This intricate case report details an exceptionally rare incidence of ovarian metastasis originating from a primary lung adenocarcinoma (LUAD). The relative rarity of this metastatic pathway in medical literature indicates significant diagnostic challenges. This patient was initially found to have both the ovarian tumor and lung nodule and they were originally considered independent primary tumors, derived from radiological interpretations and biomarker profiling. Nevertheless, subsequent postoperative histopathological and immunohistochemical staining evaluations identified ovarian tumors as invasive adenocarcinoma metastasized from lung. The lung and ovary tumor both showed marked anaplastic lymphoma kinase gene (ALK) protein expression by immunohistochemistry. The molecular pathologic genetic testing for lung tumor also revealed ALK rearrangement positive. The complexity of this case underscores the essentiality of maintaining a high degree of diagnostic vigilance, particularly when confronting synchronous tumors. In addition, immunohistochemical staining plays an important role in diagnosing the ovarian neoplasm's metastatic nature and determining the primary site of metastatic adenocarcinoma. For lung cancer with ovary metastasis patients, the adopting an adaptable treatment approach responsive to evolving diagnostic evidence can improve the accuracy of diagnosis and avoid excessive treatment of patients.

摘要

这份详尽的病例报告详细描述了一例极为罕见的源自原发性肺腺癌(LUAD)的卵巢转移病例。医学文献中这种转移途径相对罕见,这表明存在重大的诊断挑战。该患者最初被发现同时患有卵巢肿瘤和肺结节,基于放射学解读和生物标志物分析,它们最初被认为是独立的原发性肿瘤。然而,随后的术后组织病理学和免疫组化染色评估确定卵巢肿瘤为源自肺部的浸润性腺癌转移灶。通过免疫组化,肺和卵巢肿瘤均显示出明显的间变性淋巴瘤激酶基因(ALK)蛋白表达。对肺肿瘤进行的分子病理基因检测也显示ALK重排呈阳性。该病例的复杂性凸显了保持高度诊断警惕性的必要性,尤其是在面对同时出现的肿瘤时。此外,免疫组化染色在诊断卵巢肿瘤的转移性质和确定转移性腺癌的原发部位方面发挥着重要作用。对于伴有卵巢转移的肺癌患者,采用一种能根据不断演变的诊断证据灵活调整的治疗方法,可以提高诊断准确性并避免对患者进行过度治疗。

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