ADENOMYOEPITHELIOMA WITH CARCINOMA; EPITHELIAL-MYOEPITHELIAL CARCINOMA WITH EARLY PULMONARY METASTASIS.

Muhammad Umair Khan
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Abstract

Adenomyoepithelioma (AME) is a rare variant of breast neoplasm. It is a biphasic tumour characterized by small epithelial-lined spaces with inner luminal cells and outer of abluminal (myoepithelial) cells. Either - or both - of these two cells may rarely undergo malignant transformation. We present a case of a 61-year-old lady who arbored a mass in her right breast. She presented with few left sided pulmonary nodules as well and was initially diagnosed with extensive DCIS on core biopsy. Lung biopsy of nodule was diagnosed as epithelial myoepithelial neoplasm. Ultimately, modified radical mastectomy and pneumonectomy was performed. The final histopathological diagnosis turned out to be malignant. Adenomyoepithelioma with carcinoma; epithelial-myoepithelial carcinoma of breast with pulmonary metastasis. The malignant transformation of adenomyoepithelioma has been documented in only a limited number of cases. Benign AME often undergoes treatment through wide local excision, given its rare local recurrence. In contrast, the approach to malignant AME typically involves a mastectomy, with or without a lymph node biopsy. Metastases may manifest several years' post-primary diagnosis, even in cases of AMEs lacking atypical histological features. However, in our case metastasis was seen with in first four months of clinical presentation. Adenomyoepithelioma with carcinoma is an exceptionally rare neoplasm that may present with early metastasis, challenging the conventional findings of late metastasis as reported in studies. Consequently, the behaviour and prognosis of this entity remains a grey area, necessitating further exploration with a substantial sample size.

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腺肌瘤伴癌;上皮-肌上皮癌伴早期肺转移。
腺肌瘤(AME)是一种罕见的乳腺肿瘤。它是一种双期肿瘤,其特征是小的上皮排列空间,内腔细胞和外腔(肌上皮)细胞。这两种细胞中的任何一种或两者很少发生恶性转化。我们报告一位61岁的女士,右乳房有肿块。她也表现出很少的左侧肺结节,最初在核心活检中被诊断为广泛的DCIS。肺活检结节诊断为上皮性肌上皮性肿瘤。最终行改良乳房根治术和全肺切除术。最后的组织病理学诊断结果为恶性。腺肌瘤伴癌;乳腺上皮-肌上皮癌伴肺转移。腺肌瘤的恶性转化仅在少数病例中有文献记载。鉴于其罕见的局部复发,良性AME通常通过广泛的局部切除来治疗。相反,恶性AME的治疗方法通常包括乳房切除术,伴或不伴淋巴结活检。即使在没有非典型组织学特征的AMEs病例中,转移也可能在原发诊断后几年出现。然而,在我们的病例中,在临床表现的前四个月就出现了转移。腺肌瘤伴癌是一种非常罕见的肿瘤,可能出现早期转移,挑战了研究报道的晚期转移的传统发现。因此,该实体的行为和预后仍然是一个灰色地带,需要进一步进行大量样本量的探索。
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