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36岁女性以乳腺浆细胞瘤为首发表现的多发性骨髓瘤

Breast Plasmacytoma as the Initial Manifestation of Multiple Myeloma in a 36-Year-Old Woman.

作者信息

Silva Maria João, Patel Janki, Huang Alice, Lo Gullo Roberto, Pinker-Domenig Katja

机构信息

Radiology, Unidade Local de Saúde de Trás-os-Montes e Alto Douro, Vila Real, PRT.

Breast Radiology, Columbia University Irving Medical Center, New York, USA.

出版信息

Cureus. 2025 Jul 14;17(7):e87929. doi: 10.7759/cureus.87929. eCollection 2025 Jul.

Abstract

Extramedullary plasmacytomas (EMPs) of the breast are extremely rare and may present as the initial manifestation of multiple myeloma (MM). We report the case of a 36-year-old woman who presented with a rapidly growing right breast mass. Mammography and ultrasound revealed an oval, circumscribed, heterogeneous, vascular mass, measuring up to 4.2 cm, categorized as Breast Imaging Reporting and Data System (BI-RADS) 4. Core needle biopsy revealed a plasmablastic/plasmacytic neoplasm with strong CD138 expression, lambda light chain restriction, high Ki-67 index, and negative Epstein-Barr virus early RNA in situ hybridization (EBER-ISH), consistent with plasmablastic plasmacytoma. Systemic staging confirmed the diagnosis of MM, and the patient underwent chemotherapy followed by autologous stem cell transplantation. This case illustrates how breast plasmacytoma (BP) can mimic primary breast malignancies on imaging, particularly triple-negative invasive ductal carcinoma, lymphoma, or malignant phyllodes tumor. Although rare, it should be considered in younger patients with atypical breast masses. Diagnosis relies on biopsy with histopathological and immunophenotypic confirmation. Early recognition and biopsy are key, as BP may mimic aggressive breast malignancies and carry prognostic significance in MM.

摘要

乳腺髓外浆细胞瘤(EMPs)极为罕见,可能是多发性骨髓瘤(MM)的初始表现。我们报告一例36岁女性,她因右乳肿块迅速增大前来就诊。乳房X线摄影和超声检查显示为一个椭圆形、边界清晰、不均匀、有血管的肿块,最大直径达4.2 cm,分类为乳腺影像报告和数据系统(BI-RADS)4类。粗针活检显示为浆母细胞/浆细胞性肿瘤,CD138表达强,λ轻链限制,Ki-67指数高,爱泼斯坦-巴尔病毒早期RNA原位杂交(EBER-ISH)阴性,符合浆母细胞性浆细胞瘤。全身分期确诊为MM,患者接受了化疗,随后进行了自体干细胞移植。该病例说明了乳腺浆细胞瘤(BP)在影像学上如何模仿原发性乳腺恶性肿瘤,特别是三阴性浸润性导管癌、淋巴瘤或恶性叶状肿瘤。虽然罕见,但在患有非典型乳腺肿块的年轻患者中应予以考虑。诊断依赖于活检及组织病理学和免疫表型确认。早期识别和活检是关键,因为BP可能模仿侵袭性乳腺恶性肿瘤,且在MM中具有预后意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1025/12351514/8327db6429d7/cureus-0017-00000087929-i01.jpg

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