Van Hoeven K H, Drudis T, Cranor M L, Erlandson R A, Rosen P P
Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York 10021.
Am J Surg Pathol. 1993 Mar;17(3):248-58. doi: 10.1097/00000478-199303000-00005.
Low-grade adenosquamous carcinoma of the breast is an uncommon neoplasm of uncertain pathogenesis, clinical behavior, and malignant potential. This report describes the clinical and pathologic features of 32 cases of low-grade adenosquamous carcinoma. All patients presented with palpable tumors ranging from 0.6 to 8.6 cm (mean, 2.8 cm). Origin from an intraductal papillary tumor was found in 12 cases, including three with adenomyoepitheliomatous features. Electron microscopy disclosed glandular and squamous differentiation; the squamous cells often lined ducts that were structurally analogous to the acrosyringium of the eccrine sweat gland. Treatment consisted of mastectomy (13 patients) or excisional biopsy (19 patients). A single lymph node in one patient with a 3.5-cm primary carcinoma harbored metastatic adenocarcinoma. Axillary dissection revealed no metastases in 11 other patients. Another patient with an 8.0-cm breast tumor had metastatic adenosquamous carcinoma in the lung at initial diagnosis. After follow-up of 12 to 124 months, 20 of 25 patients had no recurrence. Five women treated by excisional biopsy had local recurrences in the breast. In one patient, the local recurrence was ultimately fatal due to invasion of the hemithorax. Estrogen and progesterone receptor studies were negative in 13 of 15 cases studied by biochemical analysis. The two tumors that were hormone-receptor positive were histologically associated with a papilloma and an adenomyoepithelioma, respectively. In the latter case, immunohistochemical studies showed the carcinoma to be hormone-receptor negative. Hormone receptor activity was limited to the adenomyoepitheliomatous component. This study confirms the largely indolent, but locally aggressive, clinical course of low-grade adenosquamous carcinoma of the breast. Although complete limited excision of small lesions may be curative, tumors greater than 3.0 cm may require more aggressive therapy.
乳腺低级别腺鳞癌是一种发病机制、临床行为及恶性潜能均不确定的罕见肿瘤。本报告描述了32例乳腺低级别腺鳞癌的临床和病理特征。所有患者均表现为可触及的肿瘤,大小为0.6至8.6厘米(平均2.8厘米)。12例起源于导管内乳头状瘤,其中3例具有腺肌上皮瘤样特征。电子显微镜检查显示有腺性和鳞状分化;鳞状细胞常衬于结构类似于小汗腺顶泌汗腺管的导管内。治疗方法包括乳房切除术(13例患者)或切除活检(19例患者)。1例原发性癌为3.5厘米的患者,其单个淋巴结有转移性腺癌。腋窝清扫显示其他11例患者无转移。另1例乳房肿瘤为8.0厘米的患者在初诊时肺部有转移性腺鳞癌。经过12至124个月的随访,25例患者中有20例无复发。5例接受切除活检治疗的女性乳房出现局部复发。1例患者因半侧胸腔受侵,局部复发最终导致死亡。15例经生化分析研究的病例中,13例雌激素和孕激素受体研究为阴性。2例激素受体阳性的肿瘤在组织学上分别与乳头状瘤和腺肌上皮瘤相关。在后一种情况下,免疫组化研究显示癌组织激素受体为阴性。激素受体活性仅限于腺肌上皮瘤样成分。本研究证实了乳腺低级别腺鳞癌在很大程度上呈惰性,但具有局部侵袭性的临床病程。虽然小病灶的完全局限性切除可能治愈,但大于3.0厘米的肿瘤可能需要更积极的治疗。