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一例伪装成原发性乳腺癌的转移性回肠神经内分泌肿瘤病例报告:诊断挑战与管理困境

A case report on metastatic ileal neuroendocrine neoplasm to the breast masquerading as primary breast cancer: A diagnostic challenge and management dilemma.

作者信息

Papalampros Alexandros, Mpaili Eustratia, Moris Demetrios, Sarlanis Helen, Tsoli Marina, Felekouras Evangelos, Trafalis Dimitrios T, Kontos Michael

机构信息

1st Department of Surgery, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.

Department of Surgery, Duke University Medical Center, Duke University, Durham, NC.

出版信息

Medicine (Baltimore). 2019 Apr;98(16):e14989. doi: 10.1097/MD.0000000000014989.

DOI:10.1097/MD.0000000000014989
PMID:31008928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6494217/
Abstract

RATIONALE

Metastatic neuroendocrine neoplasms (NENs) to the breast are very rare entities comprising only 1% to 2% of all metastatic breast tumors. In this article, we describe a case of a neuroendocrine ileal neoplasm metastatic to breast and liver, with breast metastatic tumor to be the initial manifestation of the disease.

PATIENT CONCERNS

We herein report a rare case of a female patient admitted to our department with a palpable painful mass on her left breast.

DIAGNOSIS

The surgical and histological investigation revealed a metastatic neuroendocrine neoplasm to the breast originated from terminal ileum.

INTERVENTIONS

A left lumpectomy, right hemicolectomy, cholecystectomy, left hepatectomy along with liver metastasectomies (V, VI, VIII) plus radiofrequency ablation of lesions to the right liver lobe plus standard lymphadenectomy was performed.

OUTCOMES

Considering the advanced stage of the disease, the patient received an adjuvant therapy of somatostatin analog plus everolimus. Under the guidance of oncological consultation, patients follow-up with CT and MRI scan and clinical re-evaluations in the first 3 and 6 months, substantiates no evidence of recurrence and she presents herself asymptomatic.

LESSONS

An appropriate level of suspicion and selective immunohistochemistry in these cases, particularly where no prior history of a known primary neuroendocrine neoplasm occurs, may help to diagnose a previously undetected neuroendocrine tumor elsewhere in the body and provide guidance for the appropriate treatment selection.

摘要

理论依据

转移性神经内分泌肿瘤(NENs)转移至乳腺是非常罕见的情况,仅占所有转移性乳腺肿瘤的1%至2%。在本文中,我们描述了一例神经内分泌性回肠肿瘤转移至乳腺和肝脏的病例,其中乳腺转移瘤是该疾病的首发表现。

患者情况

我们在此报告一例罕见病例,一名女性患者因左乳可触及疼痛性肿块入住我科。

诊断

手术及组织学检查显示,乳腺的转移性神经内分泌肿瘤起源于回肠末端。

干预措施

进行了左乳肿块切除术、右半结肠切除术、胆囊切除术、左肝切除术及肝转移瘤切除术(V、VI、VIII段),同时对右肝叶病变进行射频消融,并进行标准淋巴结清扫术。

结果

考虑到疾病的晚期阶段,患者接受了生长抑素类似物加依维莫司的辅助治疗。在肿瘤学会诊的指导下,患者在最初3个月和6个月进行了CT和MRI扫描及临床重新评估,结果显示无复发迹象,且患者无症状。

经验教训

在这些病例中,尤其是在没有已知原发性神经内分泌肿瘤既往史的情况下,保持适当的怀疑程度并进行选择性免疫组化,可能有助于诊断身体其他部位先前未被发现的神经内分泌肿瘤,并为适当的治疗选择提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee8d/6494217/ee289f2f1b3f/medi-98-e14989-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee8d/6494217/a8cea80a2f71/medi-98-e14989-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee8d/6494217/5ae1e01a28f3/medi-98-e14989-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee8d/6494217/ee289f2f1b3f/medi-98-e14989-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee8d/6494217/a8cea80a2f71/medi-98-e14989-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee8d/6494217/5ae1e01a28f3/medi-98-e14989-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee8d/6494217/ee289f2f1b3f/medi-98-e14989-g003.jpg

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Update on Surgical Management of Small Bowel Neuroendocrine Tumors.小肠神经内分泌肿瘤外科治疗的最新进展
Anticancer Res. 2018 Mar;38(3):1267-1278. doi: 10.21873/anticanres.12349.
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Neuroendocrine Neoplasms of the Appendix: A Review of the Literature.阑尾神经内分泌肿瘤:文献综述
Anticancer Res. 2018 Feb;38(2):601-611. doi: 10.21873/anticanres.12264.
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Metastatic carcinoid tumor to the breast: report of two cases and review of the literature.乳腺转移性类癌肿瘤:两例报告及文献复习
Clin Imaging. 2017 Mar-Apr;42:88-92. doi: 10.1016/j.clinimag.2016.10.011. Epub 2016 Oct 17.
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Occult Primary Neuroendocrine Tumor Metastasis to the Breast Detected on Screening Mammogram.筛查乳腺钼靶检查发现隐匿性原发性神经内分泌肿瘤转移至乳腺
J Clin Imaging Sci. 2016 Sep 29;6:41. doi: 10.4103/2156-7514.191439. eCollection 2016.
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