Aricò Francesco Marcello, Portaluri Antonio, Catanzariti Francesca, Condorelli Elvira, Aricò Demetrio, Zagami Mariagiovanna, Magliolo Emilia, Monforte Sara, Marino Maria Adele
Diagnostic and Interventional Radiology Unit, BIOMORF Department, University Hospital "Policlinico G. Martino", 98124 Messina, Italy.
Department of Nuclear Medicine, Humanitas Oncological Centre of Catania, 95125 Catania, Italy.
Diagnostics (Basel). 2025 Mar 28;15(7):860. doi: 10.3390/diagnostics15070860.
Metastases to the breast from non-mammary malignancies are rare, accounting for 0.1-5% of all breast malignancies. Neuroendocrine tumors (NETs) rarely metastasize to the breast. PET-CT somatostatin receptor imaging plays a pivotal role in the staging and follow-up of NETs, leveraging tracers like 68Ga-DOTATOC that bind to somatostatin receptors (SSTRs) expressed on tumor cells. While both primary and metastatic NETs express SSTRs, primary breast tumors may also exhibit an uptake of 68Ga-somatostatin analogs, making the differential diagnosis between primary breast tumors and neuroendocrine metastases challenging. Additionally, imaging characteristics of breast metastases from NETs are poorly documented in the literature, posing a diagnostic challenge that extends to pathology, particularly when in the absence of clinical suspicion. Misdiagnosis in such cases can lead to inappropriate therapeutic interventions. We report the case of a 75-year-old female patient with a history of pancreatic NET who presented to our breast clinic for further evaluation of a breast mass after a PET-CT scan revealed moderate 68Ga-DOTATOC uptake. Multimodality breast examination, including mammography and multiparametric US with B-mode, Color Doppler, Strain Elastography (SE), Shear Wave Elastography (SWE), and contrast-enhanced US (CEUS), was performed. Following a core biopsy, the lesion underwent surgical excision, revealing the diagnosis of NET metastasis. This case highlights a rare instance of neuroendocrine tumor metastasis to the breast, assessed using various ultrasound techniques, with detailed imaging and quantitative analysis. The comprehensive multimodal assessment contributes to the limited body of literature and provides elements for the differential diagnosis of a rare breast lesion that should always be considered in the presence of a known primary NET.
非乳腺恶性肿瘤转移至乳腺的情况较为罕见,占所有乳腺恶性肿瘤的0.1 - 5%。神经内分泌肿瘤(NETs)很少转移至乳腺。PET - CT生长抑素受体成像在NETs的分期和随访中起着关键作用,利用如68Ga - DOTATOC等与肿瘤细胞上表达的生长抑素受体(SSTRs)结合的示踪剂。虽然原发性和转移性NETs均表达SSTRs,但原发性乳腺肿瘤也可能摄取68Ga - 生长抑素类似物,这使得原发性乳腺肿瘤与神经内分泌转移瘤的鉴别诊断具有挑战性。此外,NETs乳腺转移的影像学特征在文献中记载较少,这给诊断带来了挑战,在病理学方面也是如此,尤其是在缺乏临床怀疑的情况下。此类病例的误诊可能导致不恰当的治疗干预。我们报告一例75岁女性患者,有胰腺NET病史,在PET - CT扫描显示乳腺肿块有中度68Ga - DOTATOC摄取后,到我们的乳腺诊所进行进一步评估。进行了多模态乳腺检查,包括乳腺X线摄影以及采用B超、彩色多普勒、应变弹性成像(SE)、剪切波弹性成像(SWE)和超声造影(CEUS)的多参数超声检查。在进行粗针活检后,对病变进行了手术切除,确诊为NET转移。该病例突出了神经内分泌肿瘤转移至乳腺的罕见情况,使用了各种超声技术进行评估,并进行了详细的影像学和定量分析。全面的多模态评估为有限的文献资料做出了贡献,并为一种罕见乳腺病变的鉴别诊断提供了依据,在已知原发性NET存在时应始终考虑这种情况。