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男性乳腺肌纤维母细胞瘤:一例报告及文献复习

Mammary myofibroblastoma of the male breast: a case report and literature review.

作者信息

Elayyan R, Rizk M, Shah C, Price R, Garg N

机构信息

King's College Hospital NHS Foundation Trust, UK.

出版信息

Ann R Coll Surg Engl. 2024 Oct 22. doi: 10.1308/rcsann.2024.0076.

DOI:10.1308/rcsann.2024.0076
PMID:39435535
Abstract

Mammary myofibroblastoma (MFB) is a rare benign spindle cell tumour predominantly affecting males, but also observed in postmenopausal females. Its diagnosis remains challenging owing to overlapping histological features with malignant lesions and limited tissue sampling in core biopsies. We present a case of incidentally discovered mammary MFB in a 63-year-old man and review its clinical, radiological and histopathological characteristics. The patient, who had a history of distal pancreatectomy and splenectomy, presented with an incidental left anterior chest wall nodule discovered on computed tomography scan. Clinical examination revealed a benign left retroareolar lump, confirmed by breast ultrasound and mammography. Ultrasound-guided core biopsy demonstrated characteristic spindle cells, prompting immunohistochemical staining confirming the diagnosis of MFB. The lesion was surgically excised with clear margins. Mammary MFB is commonly seen in postmenopausal women and older men, presenting as painless, mobile breast lumps. Imaging findings are nonspecific, resembling fibroadenomas or fat necrosis. Histologically, MFB lacks mammary ducts or lobules and displays characteristic spindle cells with collagenous stroma. Immunohistochemistry aids in differentiating it from other spindle cell tumours. Surgical excision is curative, with no reported cases with recurrence. Mammary MFB should be considered in the differential diagnosis of breast masses in males and postmenopausal women. Despite the challenges in diagnosis, its benign nature and favourable prognosis warrant timely recognition and appropriate management through surgical excision. Further research is needed to establish clear management guidelines and explore its underlying pathogenesis.

摘要

乳腺肌纤维母细胞瘤(MFB)是一种罕见的良性梭形细胞瘤,主要影响男性,但也见于绝经后女性。由于其组织学特征与恶性病变重叠且在粗针活检中组织取样有限,其诊断仍然具有挑战性。我们报告一例63岁男性偶然发现的乳腺MFB病例,并回顾其临床、放射学和组织病理学特征。该患者有远端胰腺切除术和脾切除术史,因计算机断层扫描偶然发现左前胸壁结节。临床检查发现左侧乳晕后有一个良性肿块,经乳腺超声和乳腺X线摄影证实。超声引导下粗针活检显示特征性梭形细胞,经免疫组化染色确诊为MFB。病变手术切除,切缘清晰。乳腺MFB常见于绝经后女性和老年男性,表现为无痛、可移动的乳腺肿块。影像学表现无特异性,类似纤维腺瘤或脂肪坏死。组织学上,MFB缺乏乳腺导管或小叶,显示特征性梭形细胞和胶原性间质。免疫组化有助于将其与其他梭形细胞瘤鉴别。手术切除可治愈,尚无复发报道。在男性和绝经后女性乳腺肿块的鉴别诊断中应考虑乳腺MFB。尽管诊断存在挑战,但其良性性质和良好预后值得通过手术切除及时识别和适当处理。需要进一步研究以建立明确的管理指南并探索其潜在发病机制。

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