“Reverse axillary mapping in early stage breast cancer Is it oncologically safe? A feasibity study

Balasubramanian V MCh, Sridevi, S. Vathulru, Asish Jakhetiya
{"title":"“Reverse axillary mapping in early stage breast cancer Is it oncologically safe? A feasibity study","authors":"Balasubramanian V MCh, Sridevi, S. Vathulru, Asish Jakhetiya","doi":"10.9790/0853-160701110115","DOIUrl":null,"url":null,"abstract":"Background: Arm lymphatics draining through the axilla are frequently disrupted during surgery for carcinoma breast leading to lymphedema. Techniques for differential identification of arm lymphatics might enable their preservation, and probable reduction in lymphedema. Aims: To evaluate the efficacy and oncological safety of reverse axillary mapping (RAM) in patients with early stage breast carcinoma and to correlate with post operative pathological nodal status. Methods and Material: It is a prospective pilot study, conducted at a tertiary care cancer speciality hospital, among patients with early stage breast cancer ( cT1/T2 cN1M0) planned for straight surgery, consenting to be part of the study. Patients were subjected to injection of blue dye (total 1 ml) at the time of surgery. During axillary dissection, lymphnodes taking up blue dye, were identified, dissected out and sent separately for pathological assessment . Results: RAM technique with blue dye identified arm lymphatic in ipsilateral axilla in 72.22%. Blue lymph nodes were identified in 61.11%. Postoperatively 13 out of 18 patients were staged as pN0, two as pN1, and three as pN3. RAM identified arm lymph nodes were free of diseases in all the patients with pN0,pN1 patients, only one of the three pN3 patients showed metastatic involvement . ( all pN3 patients could be identified as suspicious of having high nodal disease intraoperatively) Conclusions: Reverse axillary mapping can be used to identify the arm lymphatics in the ipsilateral axilla and these nodes are found to be free of metastatic disease in early stage breast cancer. I. Background Lymphatic drainage of the breast and ipsilateral upper limb is through the axilla. Majority of the cases, the two lymphatic pathways are different[1] Technique, that can differentially identify the upper limb lymphatic in the axilla can help preventing disruption of arm lymphatics at the time of axillary dissection for breast cancer. This may help reduce lymphedema, the most significant morbidity associated with surgical management of breast cancer. Reverse axillary mapping (RAM) technique, is a recent development, aimed at identifying the arm lymphatics in axilla at the time of axillary surgery for carcinoma breast. Various techniques have been described for the same using blue dye ,radioisotope or fluorescence imaging[2–5]. Although arm and breast lymphatics have been postulated to have differential drainage crossover has been documented in 2-18% [1,5–7] with pathologically proven involvement of nodes draining the arm by metastatic carcinoma from breast in 043%[5,7–11]. Most common complication associated with this procedure has been local tattoing lasting from few weeks to as long as 6 months. We aim to evaluate the efficacy of identification of arm lymphatic using low volume methylene blue injection (1-1.5 ml) and the degree of involvement of RAM identified nodes by metastatic disease among women with early stage breast cancer. II. Methods The study was conducted as a prospective non randomised study. It was conducted in the Division of breast oncology, Department of Surgical oncology at our tertiary care centre. Subjects Female patients with early stage breast cancer (cT1/T2) satisfying the exclusion criteria, with soft clinically palpable node (cN1) after routine metastatic work up , consenting to be a part of study were included in the study. Written informed consent , explaining the procedure and possible complications were taken from the patients in local language. A total of 18 patients were included in the study. “Reverse axillary mapping in early stage breast cancer Is it oncologically safe ? A feasibity study” DOI: 10.9790/0853-160701110115 ww.iosrjournals.org 111 | Page Exclusion criteria: Age < 18 yrs and more than 70 years Patients medically unfit for surgery Patients not consenting to be a part of the study Patients with history of previous surgery to ipsilateral axilla or arm. Patients with clinically N2/N3 nodes Technique Reverse axillary mapping protocol: Patients included in the study were subjected to injection of methylene blue to a total volume of 1-1.5 ml (a combination of intradermal and subcutaneous injection) , given under general anaesthesia , prior to commencement of surgery . Intradermal injection was given using an insulin syringe, and subcutaneous injection using 2 ml syringe with 26 gauze needle. All injections were given at the intermuscular groove in the medial aspect at the junction upper and middle third of the arm. Time from injection to the time of axillary dissection was noted. Careful and meticulous search for blue lymphatics were done at the start of axillary dissection to identify arm lymphatics. The position of the lymphatics/nodes were documented in relation to axillary vein, thoraco dorsal pedicle and intercostobrachial nerve. Blue nodes were dissected out and separately sent for histopathological analysis and routine axillary dissection was done to include levels 1,2 and 3, limiting dissection to tissue below the axillary vein. Intraoperative assessment of the extent of axillary nodal disease was done to identify extensive disease and was correlated with post operative histopathology. Postoperative morbidity associated with the procedure was recorded . Patients were stratified based on the postoperative nodal status and degree of involvement of arm lymph nodes by metastatic disease assessed for each category (pNO,pN1,pN2,pN3). Statistical Analysis: Statistical analysis was performed using the SPSS Statistical Software (version 17). III. Results The median age of patients included was 51.44 years (34-60 years). Three of the 18 patients had underwent excision biopsy outside. Thirteen patients has clinically T2 lesion and 3 patients had clinically T1 lesions. Based on location of the primary tumour, upper outer quadrant (11) was the most common location, followed by upper inner quadrant (4), lower outer quadrant (1), lower inner quadrant(1) and central sector(1). Preoperative diagnosis of malignancy was available for all the patients (fine aspiration cytology (4), core needle biopsy (11) and slide review (3)). Intra ductal carcinoma NOS was the most common histology, one with neuroendocrine differentiation one with poorly differentiated carcinoma with neuro endocrine differentiation. Sixteen patients had grade 3 tumours, 2 patients with grade 2 tumours (Table 1). Modified radical mastectomy was performed in 15 of 18 patients, breast conservation surgery in 2 patients and axillary lymph node dissection(ALND) alone in one patient . Mean time from injection to axillary dissection was 41.07 minutes. Mean lymph node yield was 17.9 (range 11-32). Five patients had positive nodes in axilla on final histopathological assessment [pN1 in two ( one and two nodes positive ), pN3 in 3 patients(10,12 and 16 nodes positive)].All the three patients with pN3 could be identified intra operatively as suspicious of having high nodal involvement. Blue lymphatics(RAM lymphatics) were identified in 13 out of 18 patients (72.22%) and blue lymphnodes were identified in 11 of 18 patients (61.11%).Mean duration between the injection and start of axillary dissection was41.27 minutes. The blue nodes/lymphatics were most commonly located within a centimetre below the axillary vein , just lateral to thoracodorsal pedicle (9/11 patients) , anterior to the axillary vein(1) and just inferior to the vein (1).(Fig 1) Mean yield of blue lymph node was 1.83 (range 1-3). The size of the blue lymphnode was variable ranging from 4 mm to 1.7 cm . Only one of the 11 patients in whom RAM lymph node was identified and removed, was positive for metastatic disease( had a high axillary nodal disease, pN3) (Fig 2) .Four of the 18 patients had minimal staining at the injection site, two patients complained of minimal pain at first review (2 weeks post surgery), one had a superficial epidermal loss and at the injection site . IV. Discussion Globally breast cancer is the most common cancer among women. The management of breast cancer has evolved over the years from most radical Halstead’s Radical mastectomy through breast conservation surgery to sentinel node biopsy (SLNB), with a significant reduction in the morbidity associated with the procedure. The status of axilla is one of the most important predictors of disease outcome. Most important morbidity associated with breast cancer surgery is ipsilateral lymphedema. Lymphedema incidence has a direct relationship to the extent of axillary lymph node dissection(ALND), varying from 58.4 % with radical mastectomy [12] to as low as 5 %with sentinel lymph node techniques[13].Though Z0011 trial showed that SLNB alone without ALND was not inferior in terms of local recurrence and survival [14], still the standard “Reverse axillary mapping in early stage breast cancer Is it oncologically safe ? A feasibity study” DOI: 10.9790/0853-160701110115 ww.iosrjournals.org 112 | Page practice is to perform an axillary dissection in women with positive SLNB. Cadaveric studies tracing the lymphatic of upper limb , has shown that there are two pathways, a superficial and deep pathway , most of which drain into a single sentry node in the axilla[15]. Post ALND, most of these pathways become fibrosed, impairing lymphatic drainage of he upper limb, with opening of new lymphatics in some patients[16]. Lymphatics from the ipsilateral upper limb and breast in breast cancer patients draining into the axilla, were found to be different in 86.7 % cases, in patients undergoing ALND[1]. A number of techniques have been described in literature for the identification of arm lymphatics in the axilla, using blue dye [4,6,8], radio isotope [9] and fluorescence[17]. Rate of Identification of arm lymphatics varies from 33.3% in initial studies to as high as 91% with use of radio isotopes, [8,9]. In our study, using methylene blue dye injection, at the start of surgery, blue lymphatics were identified ","PeriodicalId":14489,"journal":{"name":"IOSR Journal of Dental and Medical Sciences","volume":"65 1","pages":"110-115"},"PeriodicalIF":0.0000,"publicationDate":"2017-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IOSR Journal of Dental and Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9790/0853-160701110115","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Background: Arm lymphatics draining through the axilla are frequently disrupted during surgery for carcinoma breast leading to lymphedema. Techniques for differential identification of arm lymphatics might enable their preservation, and probable reduction in lymphedema. Aims: To evaluate the efficacy and oncological safety of reverse axillary mapping (RAM) in patients with early stage breast carcinoma and to correlate with post operative pathological nodal status. Methods and Material: It is a prospective pilot study, conducted at a tertiary care cancer speciality hospital, among patients with early stage breast cancer ( cT1/T2 cN1M0) planned for straight surgery, consenting to be part of the study. Patients were subjected to injection of blue dye (total 1 ml) at the time of surgery. During axillary dissection, lymphnodes taking up blue dye, were identified, dissected out and sent separately for pathological assessment . Results: RAM technique with blue dye identified arm lymphatic in ipsilateral axilla in 72.22%. Blue lymph nodes were identified in 61.11%. Postoperatively 13 out of 18 patients were staged as pN0, two as pN1, and three as pN3. RAM identified arm lymph nodes were free of diseases in all the patients with pN0,pN1 patients, only one of the three pN3 patients showed metastatic involvement . ( all pN3 patients could be identified as suspicious of having high nodal disease intraoperatively) Conclusions: Reverse axillary mapping can be used to identify the arm lymphatics in the ipsilateral axilla and these nodes are found to be free of metastatic disease in early stage breast cancer. I. Background Lymphatic drainage of the breast and ipsilateral upper limb is through the axilla. Majority of the cases, the two lymphatic pathways are different[1] Technique, that can differentially identify the upper limb lymphatic in the axilla can help preventing disruption of arm lymphatics at the time of axillary dissection for breast cancer. This may help reduce lymphedema, the most significant morbidity associated with surgical management of breast cancer. Reverse axillary mapping (RAM) technique, is a recent development, aimed at identifying the arm lymphatics in axilla at the time of axillary surgery for carcinoma breast. Various techniques have been described for the same using blue dye ,radioisotope or fluorescence imaging[2–5]. Although arm and breast lymphatics have been postulated to have differential drainage crossover has been documented in 2-18% [1,5–7] with pathologically proven involvement of nodes draining the arm by metastatic carcinoma from breast in 043%[5,7–11]. Most common complication associated with this procedure has been local tattoing lasting from few weeks to as long as 6 months. We aim to evaluate the efficacy of identification of arm lymphatic using low volume methylene blue injection (1-1.5 ml) and the degree of involvement of RAM identified nodes by metastatic disease among women with early stage breast cancer. II. Methods The study was conducted as a prospective non randomised study. It was conducted in the Division of breast oncology, Department of Surgical oncology at our tertiary care centre. Subjects Female patients with early stage breast cancer (cT1/T2) satisfying the exclusion criteria, with soft clinically palpable node (cN1) after routine metastatic work up , consenting to be a part of study were included in the study. Written informed consent , explaining the procedure and possible complications were taken from the patients in local language. A total of 18 patients were included in the study. “Reverse axillary mapping in early stage breast cancer Is it oncologically safe ? A feasibity study” DOI: 10.9790/0853-160701110115 ww.iosrjournals.org 111 | Page Exclusion criteria: Age < 18 yrs and more than 70 years Patients medically unfit for surgery Patients not consenting to be a part of the study Patients with history of previous surgery to ipsilateral axilla or arm. Patients with clinically N2/N3 nodes Technique Reverse axillary mapping protocol: Patients included in the study were subjected to injection of methylene blue to a total volume of 1-1.5 ml (a combination of intradermal and subcutaneous injection) , given under general anaesthesia , prior to commencement of surgery . Intradermal injection was given using an insulin syringe, and subcutaneous injection using 2 ml syringe with 26 gauze needle. All injections were given at the intermuscular groove in the medial aspect at the junction upper and middle third of the arm. Time from injection to the time of axillary dissection was noted. Careful and meticulous search for blue lymphatics were done at the start of axillary dissection to identify arm lymphatics. The position of the lymphatics/nodes were documented in relation to axillary vein, thoraco dorsal pedicle and intercostobrachial nerve. Blue nodes were dissected out and separately sent for histopathological analysis and routine axillary dissection was done to include levels 1,2 and 3, limiting dissection to tissue below the axillary vein. Intraoperative assessment of the extent of axillary nodal disease was done to identify extensive disease and was correlated with post operative histopathology. Postoperative morbidity associated with the procedure was recorded . Patients were stratified based on the postoperative nodal status and degree of involvement of arm lymph nodes by metastatic disease assessed for each category (pNO,pN1,pN2,pN3). Statistical Analysis: Statistical analysis was performed using the SPSS Statistical Software (version 17). III. Results The median age of patients included was 51.44 years (34-60 years). Three of the 18 patients had underwent excision biopsy outside. Thirteen patients has clinically T2 lesion and 3 patients had clinically T1 lesions. Based on location of the primary tumour, upper outer quadrant (11) was the most common location, followed by upper inner quadrant (4), lower outer quadrant (1), lower inner quadrant(1) and central sector(1). Preoperative diagnosis of malignancy was available for all the patients (fine aspiration cytology (4), core needle biopsy (11) and slide review (3)). Intra ductal carcinoma NOS was the most common histology, one with neuroendocrine differentiation one with poorly differentiated carcinoma with neuro endocrine differentiation. Sixteen patients had grade 3 tumours, 2 patients with grade 2 tumours (Table 1). Modified radical mastectomy was performed in 15 of 18 patients, breast conservation surgery in 2 patients and axillary lymph node dissection(ALND) alone in one patient . Mean time from injection to axillary dissection was 41.07 minutes. Mean lymph node yield was 17.9 (range 11-32). Five patients had positive nodes in axilla on final histopathological assessment [pN1 in two ( one and two nodes positive ), pN3 in 3 patients(10,12 and 16 nodes positive)].All the three patients with pN3 could be identified intra operatively as suspicious of having high nodal involvement. Blue lymphatics(RAM lymphatics) were identified in 13 out of 18 patients (72.22%) and blue lymphnodes were identified in 11 of 18 patients (61.11%).Mean duration between the injection and start of axillary dissection was41.27 minutes. The blue nodes/lymphatics were most commonly located within a centimetre below the axillary vein , just lateral to thoracodorsal pedicle (9/11 patients) , anterior to the axillary vein(1) and just inferior to the vein (1).(Fig 1) Mean yield of blue lymph node was 1.83 (range 1-3). The size of the blue lymphnode was variable ranging from 4 mm to 1.7 cm . Only one of the 11 patients in whom RAM lymph node was identified and removed, was positive for metastatic disease( had a high axillary nodal disease, pN3) (Fig 2) .Four of the 18 patients had minimal staining at the injection site, two patients complained of minimal pain at first review (2 weeks post surgery), one had a superficial epidermal loss and at the injection site . IV. Discussion Globally breast cancer is the most common cancer among women. The management of breast cancer has evolved over the years from most radical Halstead’s Radical mastectomy through breast conservation surgery to sentinel node biopsy (SLNB), with a significant reduction in the morbidity associated with the procedure. The status of axilla is one of the most important predictors of disease outcome. Most important morbidity associated with breast cancer surgery is ipsilateral lymphedema. Lymphedema incidence has a direct relationship to the extent of axillary lymph node dissection(ALND), varying from 58.4 % with radical mastectomy [12] to as low as 5 %with sentinel lymph node techniques[13].Though Z0011 trial showed that SLNB alone without ALND was not inferior in terms of local recurrence and survival [14], still the standard “Reverse axillary mapping in early stage breast cancer Is it oncologically safe ? A feasibity study” DOI: 10.9790/0853-160701110115 ww.iosrjournals.org 112 | Page practice is to perform an axillary dissection in women with positive SLNB. Cadaveric studies tracing the lymphatic of upper limb , has shown that there are two pathways, a superficial and deep pathway , most of which drain into a single sentry node in the axilla[15]. Post ALND, most of these pathways become fibrosed, impairing lymphatic drainage of he upper limb, with opening of new lymphatics in some patients[16]. Lymphatics from the ipsilateral upper limb and breast in breast cancer patients draining into the axilla, were found to be different in 86.7 % cases, in patients undergoing ALND[1]. A number of techniques have been described in literature for the identification of arm lymphatics in the axilla, using blue dye [4,6,8], radio isotope [9] and fluorescence[17]. Rate of Identification of arm lymphatics varies from 33.3% in initial studies to as high as 91% with use of radio isotopes, [8,9]. In our study, using methylene blue dye injection, at the start of surgery, blue lymphatics were identified
“早期乳腺癌的反向腋窝定位安全吗?”可行性研究
背景:在乳腺癌手术中,经腋窝引流的上臂淋巴管经常中断,导致淋巴水肿。鉴别手臂淋巴管的技术可能使其得以保存,并可能减少淋巴水肿。目的:探讨逆行腋窝定位(RAM)在早期乳腺癌患者中的疗效和肿瘤安全性,并与术后病理淋巴结状态的相关性。方法和材料:这是一项前瞻性试点研究,在一家三级护理癌症专科医院进行,患者为计划进行直接手术的早期乳腺癌(cT1/T2 cN1M0),同意成为研究的一部分。患者在手术时注射蓝色染料(共1ml)。腋窝清扫时,发现染有蓝色的淋巴结,分别清扫后送病理检查。结果:蓝染RAM技术对同侧腋窝淋巴的鉴别率为72.22%。蓝色淋巴结占61.11%。术后18例患者中13例为pN0型,2例为pN1型,3例为pN3型。在所有pN0和pN1患者中,RAM发现手臂淋巴结无病变,3例pN3患者中只有1例出现转移灶。(所有pN3患者术中均可发现疑似高淋巴结病变)结论:早期乳腺癌可采用腋窝逆测图识别同侧腋窝的上臂淋巴管,这些淋巴结无转移性。背景:乳房和同侧上肢的淋巴引流通过腋窝。多数情况下,两种淋巴通路不同[1]。鉴别腋窝内上肢淋巴的技术,有助于预防乳腺癌腋窝清扫时上肢淋巴的破坏。这可能有助于减少淋巴水肿,这是与乳腺癌手术治疗相关的最重要的发病率。逆腋窝定位(RAM)技术是近年来发展起来的一项技术,目的是在乳腺癌腋窝手术时识别腋窝内的上臂淋巴管。已经描述了使用蓝色染料、放射性同位素或荧光成像的各种技术[2-5]。虽然手臂和乳房淋巴管被认为有不同的引流交叉,但有2-18%的文献证明[1,5 - 7],病理证实043%的淋巴结被乳房转移癌累及[5,7 - 11]。这种手术最常见的并发症是局部纹身,持续时间从几周到长达6个月。我们的目的是评估使用小体积亚甲基蓝注射(1-1.5 ml)识别手臂淋巴的有效性,以及早期乳腺癌女性转移性疾病对RAM识别淋巴结的侵犯程度。2方法采用前瞻性非随机对照研究。它是在我们三级保健中心外科肿瘤科乳腺肿瘤科进行的。研究对象:符合排除标准的早期乳腺癌(cT1/T2)女性患者,经常规转移性检查后临床可触及软淋巴结(cN1),同意参与研究。用当地语言向患者索取书面知情同意书,说明手术过程和可能的并发症。研究共纳入18例患者。“早期乳腺癌的反向腋窝定位安全吗?”一项可行性研究“DOI: 10.9790/0853-160701110115”排除标准:年龄< 18岁和70岁以上医学上不适合手术的患者不同意成为研究的一部分既往有同侧腋下或手臂手术史的患者。临床N2/N3淋巴结患者技术腋窝反向定位方案:纳入研究的患者在手术开始前,在全身麻醉下注射亚甲基蓝,总体积为1-1.5 ml(皮内和皮下注射的组合)。胰岛素注射器皮内注射,26纱布针2 ml注射器皮下注射。所有注射均在臂上和中三分之一交界处内侧的肌间沟进行。记录注射至腋窝解剖时间。在腋窝清扫开始时仔细细致地寻找蓝色淋巴管,以确定上臂淋巴管。淋巴结的位置与腋窝静脉、胸背蒂和肋间臂神经有关。 切除蓝色淋巴结,分别送去做组织病理学分析,并进行常规腋窝清扫,包括1、2和3层,将清扫限制在腋窝静脉以下组织。术中对腋窝淋巴结病变的程度进行评估,以确定广泛的疾病,并与术后组织病理学相关。记录与手术相关的术后发病率。根据术后淋巴结状态和手臂淋巴结转移程度(pNO、pN1、pN2、pN3)对患者进行分层。统计分析:采用SPSS统计软件(version 17)进行统计分析。3结果患者中位年龄为51.44岁(34 ~ 60岁)。18例患者中有3例在室外进行了切除活检。临床T2病变13例,临床T1病变3例。根据原发肿瘤的位置,上外象限(11)是最常见的位置,其次是上内象限(4)、下外象限(1)、下内象限(1)和中央区(1)。所有患者术前均可获得恶性肿瘤诊断(细吸细胞学检查4例,穿刺活检11例,切片检查3例)。导管内癌以NOS最常见,1例伴神经内分泌分化,1例伴神经内分泌分化的低分化癌。16例为3级肿瘤,2例为2级肿瘤(表1)。18例患者中有15例行改良根治性乳房切除术,2例行保乳手术,1例单独行腋窝淋巴结清扫术(ALND)。从注射到腋窝清扫平均时间为41.07分钟。平均淋巴结清扫率为17.9(范围11-32)。5例患者在最终组织病理学评估中腋窝淋巴结阳性[2例pN1(1和2个淋巴结阳性),3例pN3(10、12和16个淋巴结阳性)]。所有3例pN3患者术中均被认为有高淋巴结受累的嫌疑。18例患者中有13例(72.22%)发现蓝色淋巴,11例(61.11%)发现蓝色淋巴结。注射至腋窝清扫开始的平均时间为41.27分钟。蓝色淋巴结/淋巴管最常位于腋窝静脉下方1厘米内,胸背蒂外侧(9/11),腋窝静脉前方(1)和静脉下方(1)。(图1)蓝色淋巴结的平均产率为1.83(范围1-3)。蓝色淋巴结的大小从4mm到1.7 cm不等。在11例发现并切除RAM淋巴结的患者中,只有1例转移性疾病阳性(有高腋窝淋巴结疾病,pN3)(图2)。18例患者中有4例在注射部位有轻微的染色,2例患者在第一次复查时(手术后2周)有轻微的疼痛,1例在注射部位有浅表表皮脱落。在全球范围内,乳腺癌是女性中最常见的癌症。多年来,乳腺癌的治疗已经从最根治性的Halstead根治性乳房切除术,到乳房保留手术,再到前哨淋巴结活检(SLNB),显著降低了与手术相关的发病率。腋窝的状态是疾病预后最重要的预测指标之一。与乳腺癌手术相关的最重要的发病率是同侧淋巴水肿。淋巴水肿的发生率与腋窝淋巴结清扫(ALND)的程度有直接关系,从根治性乳房切除术的58.4%[12]到前哨淋巴结清扫术的5%[13]不等。虽然Z0011试验显示单纯SLNB不加ALND在局部复发率和生存率方面并不差[14],但标准的“早期乳腺癌腋窝反向作图是否肿瘤安全?”一项可行性研究“DOI: 10.9790/0853-160701110115网址:iosrjournals.org 112 |页的做法是执行腋窝解剖的妇女积极SLNB。在尸体上追踪上肢淋巴的研究表明,淋巴有两条通路,浅层和深层,其中大部分流入腋窝的一个哨兵淋巴结[15]。ALND后,大多数这些通路纤维化,损害上肢的淋巴引流,在一些患者中出现新的淋巴管开放[16]。在接受ALND的乳腺癌患者中,86.7%的患者发现来自同侧上肢和乳房的淋巴管流入腋窝的情况不同[1]。文献中描述了许多技术用于鉴定腋下的手臂淋巴管,使用蓝色染料[4,6,8],放射性同位素[9]和荧光[17]。上臂淋巴管的鉴别率从33%不等。 在使用放射性同位素时,从最初的3%增加到高达91%,[8,9]。在我们的研究中,使用亚甲基蓝染料注射,在手术开始时,确定了蓝色淋巴管
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