Lamichhane Nirmal, Pradhan Manohar, Neupane Prakash Raj, Shrestha Bhakta Man, Dhakal Hari Prasad, Thakur Binay Kumar, Cox Charles Evandor
Department of Surgical Oncology, B P Koirala Memorial Cancer Hospital, Bharatpur, Nepal.
Nepal Med Coll J. 2007 Mar;9(1):22-6.
To evaluate the performance and feasibility of sentinel lymph node biopsy in early breast cancer patients using patent blue dye. From March 2004, we are consecutively enrolling breast cancer patients with tumor size less than 5 cm with no clinically palpable axillary lymph nodes in this feasibility study. So far, 21 patients underwent sentinel lymph node biopsy using 1.0% patent blue dye injection around the tumor followed by axillary dissection. Sentinel lymph node biopsy was compared with axillary dissection for its ability to accurately reflect the final pathological status of the axillary nodes. Age of patients ranged form 32-67 years old with mean age of 46.72 years. Fifty seven percent of patients were postmenopausal. Patients with T1 lesions were 8 and T2 were 13. The sentinel lymph node/s were successfully identified in 20 out of 21 patients (95.0%). The number of sentinel lymph nodes ranged from 1 to 5 (average 2.0) and non-sentinel nodes ranged from 5-22 (average 12.0). Infiltrating ductal carcinoma was diagnosed in 15 patients, DCIS with early invasion in 4 patients, invasive lobular carcinoma in 1 and medullary carcinoma in 1 patient. Of the 20 patients in whom sentinel lymph nodes were successfully identified, nodes were positive in 35.0% (7/20) of patients. All the positive nodes were detected in group with T2 lesions. SLNs were the only positive nodes in 2 patients. There were no false negative patients, yielding an accuracy of 100.0%. Lymphatic mapping using patent blue dye alone is technically feasible for patients with small (T1 or T2) palpable breast tumors. The sentinel node can be reliably identified in the majority of these patients, and its histology reflects that of the axilla with a high degree of accuracy. This method is very useful in economically backward countries as it involves less expensive material.
评估使用专利蓝染料对早期乳腺癌患者进行前哨淋巴结活检的性能和可行性。自2004年3月起,在这项可行性研究中,我们连续纳入肿瘤大小小于5 cm且临床上未触及腋窝淋巴结的乳腺癌患者。到目前为止,21例患者接受了前哨淋巴结活检,方法是在肿瘤周围注射1.0%的专利蓝染料,随后进行腋窝淋巴结清扫。将前哨淋巴结活检与腋窝淋巴结清扫在准确反映腋窝淋巴结最终病理状态的能力方面进行比较。患者年龄在32至67岁之间,平均年龄为46.72岁。57%的患者为绝经后。T1期病变患者8例,T2期患者13例。21例患者中有20例(95.0%)成功识别出前哨淋巴结。前哨淋巴结数量为1至5个(平均2.0个),非前哨淋巴结数量为5至22个(平均12.0个)。15例患者诊断为浸润性导管癌,4例患者诊断为伴有早期浸润的导管原位癌,1例患者诊断为浸润性小叶癌,1例患者诊断为髓样癌。在成功识别出前哨淋巴结的20例患者中,35.0%(7/20)的患者淋巴结为阳性。所有阳性淋巴结均在T2期病变组中检测到。前哨淋巴结是2例患者唯一的阳性淋巴结。没有假阴性患者,准确率为100.0%。对于可触及的小(T1或T2)乳腺肿瘤患者,仅使用专利蓝染料进行淋巴绘图在技术上是可行的。在大多数这些患者中可以可靠地识别出前哨淋巴结,并且其组织学高度准确地反映腋窝的情况。这种方法在经济落后国家非常有用,因为它涉及成本较低的材料。