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浸润性导管乳腺癌中的破骨细胞样基质巨细胞:病例系列

Osteoclast-like stromal giant cells in invasive ductal breast cancer: A case series.

作者信息

Angellotti Giustina, Tomasicchio Giovanni, Montanaro Alda Elena, Telgrafo Michele, Mastropasqua Mauro Giuseppe, Punzo Clelia

机构信息

DETO, Department of Emergency and Organ Transplantations, Breast Care Unit, Aldo Moro University of Bari Medical School, Piazza Giulio Cesare 11, 70124 Bari, Italy.

DETO, Department of Emergency and Organ Transplantations, Breast Care Unit, Aldo Moro University of Bari Medical School, Piazza Giulio Cesare 11, 70124 Bari, Italy.

出版信息

Int J Surg Case Rep. 2022 Aug;97:107421. doi: 10.1016/j.ijscr.2022.107421. Epub 2022 Jul 16.

Abstract

INTRODUCTION

Breast Cancer with osteoclast-like stromal giant cells (OLGCs) is a rare pattern of invasive non-special type ductal carcinoma. The OLGCs are specific type of macrophage and are likely distinct from true osteoclasts. The aim of this case series was to describe the characteristics of this invasive ductal carcinoma rare histotype.

PRESENTATION OF CASES

The authors present the cases of two young women that, during national screening, discovered with mammography X-ray a breast lump suspected for malignancy. The core needle biopsy confirmed the malignancy of both nodule and in one patient the histological analysis revealed pre-operative OLGCs. In both cases the sentinel lymph node biopsy was negative therefore a quadrantectomy without axillary lymphadenectomy was done. The definitive histopathological examination was positive for invasive ductal carcinoma with OLGCs and CD 68 marker positivity. After surgery, patients underwent adjuvant therapy and multidisciplinary follow-up.

DISCUSSION

The origin and mechanism for developing osteoclast-like giant cells is unknown. The OLGCs directly descend from the precursors of the monocyte-macrophage. The rarity of this entity often promotes a misleading diagnosis, with >50 % of erroneous diagnosis of benign lesion. The prognostic significance of OLGCs in breast cancer is controversial, however it doesn't seem to influence the axillary lymph nodes spread. The presence of preoperative OLGCs didn't modify our surgical and oncological approach.

CONCLUSION

Breast Cancer with OLGCs is a rare tumour that has a similar prognosis to other carcinomas of identical grade and stage in most cases. The rarity and characteristics of this neoplasm require personalized treatments, discussed by a multidisciplinary team.

摘要

引言

伴有破骨细胞样基质巨细胞(OLGCs)的乳腺癌是浸润性非特殊类型导管癌的一种罕见模式。OLGCs是巨噬细胞的一种特殊类型,可能与真正的破骨细胞不同。本病例系列的目的是描述这种浸润性导管癌罕见组织学类型的特征。

病例介绍

作者介绍了两名年轻女性的病例,她们在国家筛查期间通过乳腺钼靶X线检查发现乳房肿块,怀疑为恶性。粗针活检证实两个结节均为恶性,其中一名患者的组织学分析显示术前存在OLGCs。在这两个病例中,前哨淋巴结活检均为阴性,因此进行了象限切除术,未进行腋窝淋巴结清扫。最终组织病理学检查显示浸润性导管癌伴OLGCs且CD 68标记阳性。手术后,患者接受了辅助治疗和多学科随访。

讨论

破骨细胞样巨细胞的起源和形成机制尚不清楚。OLGCs直接来源于单核细胞-巨噬细胞的前体。这种实体的罕见性常常导致误诊,超过50%的病例被误诊为良性病变。OLGCs在乳腺癌中的预后意义存在争议,但似乎不影响腋窝淋巴结转移。术前OLGCs的存在并未改变我们的手术和肿瘤治疗方法。

结论

伴有OLGCs的乳腺癌是一种罕见肿瘤,在大多数情况下,其预后与其他相同分级和分期的癌相似。这种肿瘤的罕见性和特征需要多学科团队讨论进行个性化治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed5/9403206/eaebe80fe29f/gr1.jpg

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