Ishida Mitsuaki, Umeda Tomoko, Abe Hajime, Tani Tohru, Okabe Hidetoshi
Department of Clinical Laboratory Medicine and Division of Diagnostic Pathology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Oncol Lett. 2012 Jul;4(1):29-32. doi: 10.3892/ol.2012.678. Epub 2012 Apr 12.
Neuroendocrine carcinoma (NEC) of the breast is a rare distinct clinicopathological entity, which, clinically, tends not to be aggressive. Mucinous carcinoma of the breast is also a rare distinct entity and is classified into types A (paucicellular) and B (hypercellular). It is well known that type B mucinous carcinoma frequently shows neuroendocrine differentiation. However, the coexistence of NEC and mucinous carcinoma within the same breast tumor is extremely rare. In the present study, we report a case of solid NEC of the breast with a mucinous carcinoma component and discuss the tumorigenesis of this extremely rare lesion. A 37-year-old Japanese female presented with a right breast tumor. Mastectomy and removal of the right axillary lymph nodes were performed. The resected breast tumor was composed of solid NEC (approximately 85% of the tumor) and type B mucinous carcinoma components. The right axillary lymph nodes had metastatic solid NEC. Three years later, local recurrence of mucinous carcinoma occurred in the operation scar of the right thoracic wall. In addition, seven years after the first surgery, metastatic solid NEC in the liver was observed. Recent molecular studies clearly revealed that no differences in gene expression are present between type B mucinous carcinoma and NEC. Therefore, the present case may represent solid NEC and type B mucinous carcinoma as part of a spectrum with the same genetic background. Moreover, the prognosis of solid NEC is thought to be good, and metastasis is extremely rare. However, metastasis of solid NEC of the breast may occur at a later stage. Therefore, long-term follow-up is required for patients with solid NEC of the breast.
乳腺神经内分泌癌(NEC)是一种罕见的独特临床病理实体,临床上往往侵袭性不强。乳腺黏液癌也是一种罕见的独特实体,分为A 型(少细胞型)和B 型(多细胞型)。众所周知,B 型黏液癌常显示神经内分泌分化。然而,同一乳腺肿瘤中NEC 和黏液癌并存极为罕见。在本研究中,我们报告了一例伴有黏液癌成分的乳腺实性NEC 病例,并讨论了这种极其罕见病变的肿瘤发生机制。一名37 岁的日本女性因右乳腺肿瘤就诊。行乳房切除术及右腋窝淋巴结清扫术。切除的乳腺肿瘤由实性NEC(约占肿瘤的85%)和B 型黏液癌成分组成。右腋窝淋巴结有转移性实性NEC。三年后,右胸壁手术瘢痕处发生黏液癌局部复发。此外,首次手术后七年,观察到肝脏有转移性实性NEC。最近的分子研究清楚地表明,B 型黏液癌和NEC 之间在基因表达上没有差异。因此,本病例可能代表具有相同遗传背景的一系列病变中的实性NEC 和B 型黏液癌。此外,实性NEC 的预后被认为良好,转移极为罕见。然而,乳腺实性NEC 的转移可能在后期发生。因此,乳腺实性NEC 患者需要长期随访。