Myoid hamartoma of breast: a rare case report with review of literature

Nimisha Dhankar, Nita Khurana, Jyoti Kumar, Sushanto Neogi
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Abstract

Myoid hamartomas of breast are extremely rare lesions with poorly defined pathogenesis. They are composed of differentiated mammary glandular and stromal structures with areas of smooth muscle differentiation. They are postulated to arise from walls of the blood vessels and/or muscularis mammillae of the areolae. They usual present as a well demarcated lump and it is difficult to diagnose them on clinical and radiological basis. Diagnosis requires demonstration of smooth muscle phenotype using immunohistochemistry by smooth muscle actin and desmin. Surgical resection is the curative treatment. We reported a case of myoid hamartoma in a 50-year-old postmenopausal lady with its clinical, radiological and histopathological discussion. The lesion presented as a painless lump and was initially reported as BIRADS 4a on mammography. Apart from the stroma showing spindle cell component with smooth muscle differentiation, the histopathology also showed epithelial changes including epithelial hyperplasia and columnar cell change.
乳房肌样错构瘤1例并文献复习
摘要乳房肌样错构瘤是极为罕见的病变,其发病机制不明确。它们由分化的乳腺和间质结构组成,并有平滑肌分化区。它们被认为起源于血管壁和/或乳晕的乳头肌层。它们通常表现为界限清楚的肿块,难以在临床和放射学基础上诊断。诊断需要使用平滑肌肌动蛋白和desmin的免疫组织化学来证明平滑肌表型。手术切除是根治性治疗。我们报告了一例50岁绝经后妇女的肌样错构瘤,并对其临床、影像学和组织病理学进行了讨论。病变表现为无痛性肿块,最初在乳房x光检查中报告为BIRADS 4a。除间质呈梭形细胞成分,平滑肌分化外,组织病理学还显示上皮增生和柱状细胞改变。
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