NucMed > Musculoskeletal > Lymph

Lymphoscintigraphy

Chemistry and Pharmacology

Tc-Antimony trisulfide colloid was previously the agent of choice for nuclear lymphoscintigraphy, but this agent is no longer commercially available. Other radiocolloids are therefore used and include Tc-sulfur micro- or nanocolloid (which is Tc-Sulfur colloid filtered through a millipore filter to eliminate all particles larger than 0.22 microns in diameter) or Tc-human serum albumin (HSA). The permeability of lymphatics to colloidal particles is maximal for particles less than 50 nm. Larger particles remain mostly at the injection site.

An inherent limitation of lymphoscintigraphy is its poor visualization of the deep lymphatic system. Web space injections highlight the superficial system only. Deep lymphatic channels originating posterior to the malleoli and coursing to the popliteal nodes and then along the superficial femoral vein are usually not identified.

Micropore filtered Tc-SC in susupended in 0.1 ml of saline and 1 mCi (37 MBq) is injected intradermally in the web interspaces of the extremities to be evaluated [20]. Tc-sulfur colloid requires an acidic pH to remain stable and this can cause the patient to experience burning at the injection site [23]. The area of injection is massaged for 2 minutes immediately after injection [20]. A resolution collimator is used and images are acquired sequentially over the extremities. A transmission scan should also be recorded to permit anatomic localization of the visualized areas [23]. In patients with normal lymphatics, a predictable sequence of tracer activity should be identified. In the lower extremities, activity normally appears in the lymphatic bundle along the anteromedial aspect of the leg. Several channels may be identified in the calf, but only one (or two) vessel(s) is seen in the thigh [20]. Bilateral visualization of the inguinal lymphatics should be seen within one hour [20], but activity can appear within the pelvic nodes within 10 minutes due to the small size of the particles. Typically one to three popliteal nodes and two to ten inguinal nodes are visualized [20]. Muscular exercise (walking) is used to enhance lymphatic flow. Abnormal findings include interruption of lymphatic flow, collateral lymph vessels, dermal backflow, delayed flow, delayed asymmetric visualization or non-visualization of lymph nodes, a reduced number of lymph nodes, dilated lymphatics, or no visualization of lymphatic channels [20].

Lymphedema:

Lymphedema results from the progressive accumulation of protein rich fluid in the interstitial spaces secondary to an anatomic or functional obstruction of the lymphatic system. Patients with lymphedema experience extremity swelling, decreased mobility, and secondary infections [20]. There is both a superficial and deep lymphatic system which drain at very different rates. The superficial system is the primary route for lymphatic drainage [23]. Deep lymphatic transport is less than 10% of the superficial transport system [23].

Primary Lymphedema:

Primary lymphedema is the result of congenital aplastic or hypoplastic lymphatics. If familial it is referred to as Noone-Milroy's disease, but this is a rare disorder and non-familial primary lymphedema is much more common. Primary lymphedema is classified by the age of onset- congenital, or praecox (prior to) and tarda (over the age of 35, respectively). The onset is usually spontaneous without history of trauma, surgery, or radiation [20]. The disorder is slowly progressive, tends to affect females (4:1 predominance) with a peak incidence at puberty, and a lower limb is involved in the majority of cases.

In patients with congenital lymphatic aplasia, scintigraphy typically demonstrates little to no removal of tracer from the injection site, no lymphatic channels, and no regional nodal activity. A decreased number and or caliber of lymphatic vessels is seen in patients with hypoplasia.

Secondary Lymphedema:

Secondary lymphedema occurs when there has been some type of insult to the normal lymphatic channels (surgery, trauma, neoplasm, or inflammation). The disorder can present months to years after the initial injury [20]. Worldwide, the most common cause is filariasis due to Wuchereria bancrofti infection. Post-surgical lymphedema is also common following axillary node dissection (5-30%) and pelvic cancer surgery (10-49%) [23]. Microangiolymphatic surgery is usually more successful in secondary lymphedema than in primary lymphedema. Scintigraphy typically demonstrates delayed transport of tracer from the injection site with dermal back flow, large collateral channels, and fewer visualized lymph nodes. Cross-over of activity from the contra-lateral normal side to pelvic nodes on the affected may also be seen and care should be taken to ensure that this finding is not misinterpreted as normal.
 

Sentinel Node Detection:

Melanoma:

Clinical: The prevalence of malignant melanoma has rapidly increased and the lifetime risk for melanoma in the United States will exceed 1% in the near future [4]. Melanoma can be cured by surgery alone when the disease is localized [21]. However, up to 20% of patients that present with melanoma and no clinical evidence of metastases harbor occult lymph node metastases. Patients at greatest risk for lymph node metastases are those with a lesion depth of more than 1 mm Breslow thickness. The incidence of sentinel lymph node metastasis is approximately 5% for melanomas between 0.76 and 1.5 mm in thickness, but increases to almost 20% for melanomas between 1.5 and 4 mm [21]. The presence of regional lymph node metastases is a very important predictor of patient 5 year survival [3,21]. Prophylactic elective lymph node dissection can result in a 50% 5 year survival rate when micrometastases are found (as compared to a 25% survival rate when patients subsequently present with enlarged lymph nodes) [3]. Unfortunately, morbidity from lymph node dissection is high. Lymphoscintigraphy with lymph node mapping can be used to better delineate the lymphatic drainage from the primary lesion. The procedure is based on the hypothesis that melanoma metastasizes to regional lymph nodes via a defined connection of dermal lymphatics which can be followed to the first or "sentinel" lymph nodes in the regional basin. The absence of tumor in the sentinal node is felt to be strongly indicative of the absence of metastases to other nodes in the regional basin (skip metastases to second or third tier lymph nodes with sparing of the sentinel node occurs in less than 2% of patients [21]). Thus, the patient could be spared extensive node dissection surgery if the sentinel nodes are negative. If the sentinel nodes are positive for tumor, then the patient would undergo a complete lymph node dissection [2]. The success rate of lymphoscintigraphy for sentinel node identification in approximately 98% [21].

Procedure: Filtered Tc-sulfur colloid (1 mCi) is injected intradermally in 4 to 6 equal doses of 0.1 to 0.2 mL about the lesion or surgical site (about 0.5 to 1 cm from the lesion) [4,21]. Small injected volumes should be used to decrease the risk of collapsing local lymphatics [21]. Only about 5-8% of the injected dose will migrate from the injection site [5]. Imaging is started immediately after injection using a large field of view detector with a parallel hole collimator, a 10% window centered on the 140-keV technetium energy peak, and a 128 x 128 matrix [4]. Dynamic images are obtained at 20-30 seconds per frame for 30 to 45 minutes to demonstrate lymphatic flow and regional drainage. Lateral or oblique static images are also acquired for 300 seconds using a 256 x 256 matrix to better depict the nodal findings [21]. An outline of the patients body should be obtained using a radioactive flood source to aid in image orientation [4]. Delayed static images at 1, 2, and 4 hours can be performed with static 5-10 minute images to evaluate all regions that could possibly drain the primary melanoma (a transmission source on the delayed images helps to highlight the body outline) [5]. Activity from the injection site may occasionally mask the regional nodes if they are located very near to each other. Shielding may be required. The sentinal node is usually evident as the primary lymphatic channel will drain to this node. More than one primary lymphatic channel may be identified and therefore, patients can have more than one sentinal node. Another benefit of lymphoscinitgraphy is that unanticipated patterns of lymphatic drainage can be identified and aid in directing surgical node dissection. Between 7.5-15% of melanoma patients can have dual drainage patterns [2]. For the procedure, the surgeon utilizes a hand-held gamma probe to identify radioactive nodes. Blue dye is also generally injected intradermally just prior to the procedure [3]. The count rate is higher in sentinal nodes and the first node in the line is usually the most radioactive [1]. Generally a count rate at least 3 times that of background [3] or a node with a count rate of at least 20% of the count rate in the hottest node is considered positive. Blue staining of the node helps to confirm that the node is the sentinel node [3]. After a positive sentinel node is identified, complete lymphadenectomy of the lymphatic basin should be performed [21]. Lymphadenectomy alone has improved the 5 year survival rate from 27% to 48% [21].

Outcome: Lymphatic mapping with sentinel node dissection has been demonstrated to be equivalent [2] and possibly superior [21] to elective lymph node dissection. The procedure can provide prognostic information based upon the presence or absence of regional lymph node metastases [3,21]. Although the procedure reduces the morbidity associated with elective lymph node dissection, lymphoscintigraphy and sentinel node dissection has not been show to result in overall disease-free survival [2]. The rate of regional lymph node recurrences is also similar between the two procedures [2]. Additionally, there is controversy about the procedure due to the lack of elective adjuvant therapy once sentinel node metastases have been identified [21].

REFERENCES:
(1) J Nucl Med 1997; Kapteijn BA, et al. Validation of gamma probe detection of the sentinal node in melanoma. 38: 362-366

(2) Ann Surg Oncol 1999; Essner R, et al. Efficacy of lymphatic mapping, sentinel node lymphadenectomy, and selective complete lymph node dissection as a therapeutic procedure for early-stage melanoma. 6: 442-449

(3) Cancer 2001; Statius Muller MG, et al. The sentinel lymph node status is an important factor for predicting clinical outcome in patients with stage I or II cutaneous melanoma. 91: 2401-08

(4) Radiographics 2002; Lymphoscintigraphy in cutaneous melanoma: a total body atlas of sentinel node mapping. 22: 491-502

(5) J Nucl Med 2003; Uren RF, et al. Patterns od lymphatic drainage from the skin in patients with melanoma. 44: 570-582

Sentinel Node Detection

Breast Cancer:

Background:

Axillary node status is required to properly stage breast cancer [3]. The presence or absence of axillary node metastases carries important prognostic information [3] and guides adjuvant therapy [18]. There is a 20-30% likelihood for the presence of axillary nodal metastases in very early breast cancers (T1a-b, tumor size less than or equal to 1 cm), and this rises to 30-40% for T1c lesions (size 1-2 cm) [18]. Clinical exam has a poor predictive value for the determination of nodal involvement and therefore histologic examination of the axillary nodes is important for the identification of metastatic disease [18]. Conventional axillary lymph node dissection involves extensive dissection of most of level I, II, and III nodes [28]. Unfortunately, conventional axillary node dissection surgery suffers from sampling error and can be complicated by significant patient morbidity (particularly lymphedema and sensory-motor disturbances in the ipsilateral arm) [3,18].

The "sentinel node" is the first lymph node encountered by lymphatic vessels draining a tumor [18]. The absence of tumor in the sentinal node (SLN) is felt to be strongly indicative of the absence of metastatic disease to other nodes in the regional basin. Thus, patients could be spared extensive node dissection surgery if the sentinel node could be identified, examined, and found to be free of tumor. Further axillary dissection could be performed only in patients with positive findings for malignancy in the sentinal node or in whom the sentinel node could not be localized. Sentinel node biopsy would represent a significant advantage as a minimally invasive procedure, considering that, after surgery, about 70% of patients with clinically N0 disease are found to be free from metastatic disease [18].

Lymphoscintigraphy has been used in the detection of the sentinal node in patients with breast cancer. The axillary sentinal node can be properly identified in 90 to 100% of patients with use of an intraoperative gamma detecting probe and blue dye [2,10,11]. The technical success rate for the exam has been reported to be between 66% to 100%. The exam has a reported sensitivity of 83-100% (roughly 95-97%), specificity of 100%, positive predictive value of 100%, negative predictive value of 92-100%, and an accuracy of 95-100% [4,18]. The exam has been shown to be highly reproducible [25], accurate [30], and associated with less morbidity compared to axillary node dissection [30].

The rationale for sentinel lymph node mapping using scintigraphy is based on the fact that under normal circumstances the breast (the mammary gland and the overlying skin) can be considered a single biological unit with a common centrifugal lymphatic pathway [29]. Lymph flows from the superficial to the deep layers and then towards regional lymph nodes through lymph channels that originate in the interlobular spaces and along lactifierous ducts [29]. The lymphatic vessels of the breast tend to accompany the routes of blood supply- mainly the axillary and internal mammary vessels [18]. Most of the lymph drains to the axillary lymph nodes [29]. About 3% drains to the internal mammary chain nodes (usually from the medial portion of the breast), and a very small percentage drains to the posterior intercostal nodes [18,29]. Part of the lower portion of the breast can drain to the lymphatic system of the upper abdominal wall, and part of the upper portion can drain to the apical axillary nodes and deep cervical nodes [18]. Thus, the pattern of lymphatic drainage can be variable and it is impossible to predict the route of drainage of a tumor based upon its location within the breast [18]. Although the presence of "skip" metastases (axillary node metastases to second-tier nodes or elsewhere with no evidence of metastases at level I) has been reported to be between 4-12% [4,18]. These "skip" lesions likely represent sentinal nodes outside level I and such nodes can be readily identified by lymphoscintigraphy [4].

Lymphoscintigraphy can provide information regarding primary lymphatic drainage to sites other than the axilla such as the inaccessible internal mammary (IM) chain (which occurs in 6-17% of cases [3,10,19,26]). Although internal mammary (IM) node drainage is more commonly seen with tumors located in the inner quadrants [19], it is important to note that up to 46% of tumors with drainage to IM nodes can be located within the outer part of the breast [10]. Drainage to sentinel nodes is more likely to be identified when peritumoral tracers injections are performed [27]. Patients with IM and axillary node metastases have a significantly worse prognosis than patients with isolated axillary node disease [19]. Despite this fact, pursuit of sentinel nodes outside the axilla is not performed at all institutions. This is because the treatment of IM nodal disease remains controversial [24]. Surgical resection of IM nodes may not reduce local-regional recurrence or improve survival [24], although aggressive radiation therapy may provide some benefit [19]. Lymphoscintigraphy does permit evaluation of IM nodes and may enable more accurate staging and spare patients unnecessary axillary node dissections [17]. 

Indications/Contraindications:

Patients who are being considered for axillary node dissection and who do not have clinically involved nodes by exam or high tumor grade (T3 or T4, tumor larger than 4 cm) are candidates for lymphoscinitgraphy. Patients with nodes that are felt to be involved by tumor on clinical exam are not candidates for lymphscinitgraphy as lymphatic flow to a node that is replaced by tumor may be obstructed and the node may not be identified (ie: incorrect localization of the sentinel node) [12,14,18]. Patients with multifocal or multicentric cancers are also generally not candidates for lymphoscintigraphy as the procedure may not reflect all possible sentinel nodes from different lesions [18,22]. However, at least one study has shown very good sensitivity and negative predictive value in this subgroup of patients [22]. Surgical biopsy can disrupt lymphatic pathways and may affect exam results [4], although other authors have found no difference in sentinel node localization following prior surgical biopsy [10,11,15]. Patients who have undergone prior surgical procedures in the axilla can have altered patterns of regional lymphatic drainage and should be evaluated on a case-by-case basis [18]. Patients that have received pre-operative chemotherapy are also not good candidates for lymphoscintigraphy as up to 33% of patients can have a false-negative result [23].

Agent/Procedure:

Tc99m-sulfur colloid (Tc-SC) is the agent most commonly used for sentinel node localization. Unfortunately, there is no standardized technique for sentinel node localization. Wide variations exist regarding particle size, timing of injection, volume and placement of the injection, use of pre-operative imaging, and operative techniques [11]. It is important to avoid skin contamination during the injection [28]. Methods to decrease skin contamination include applying negative pressure to the syringe during needle withdrawal and immediately dabbing the injection site with a gauze pad [28].

Particle size: Radiocolloids are cleared by lymphatic drainage with a speed that is inversely proportional to the particle size [18]. A particle size between 100-200 nm is probably the best compromise between the need for efficient and fast lymphatic drainage and nodal retention of the particle [18]. Particles larger than 300 nm migrate too slowly (although they are retained for a greater period of time within the sentinel node), while particles less than 50 nm progress to second or third-tier nodes too quickly [18]. The Tc-SC particle size can be reduced to aid in lymphatic uptake of the tracer. A reduction in particle size is accomplished by filtering the agent through a 200 nm millipore filter, use of shortened boiling times during preparation or by using Tc-pertechnetate of longer ingrowth [3]. Not all centers use filtered colloid as they feel there is improved/prolonged retention of the agent in the sentinal nodes when the colloid is not filtered [4,9,11]. 

pH: Some centers adjust the pH of the injected agent to neutral with sodium bicarbonate [5].

Injection site: Peri-tumoral, intradermal, or intra-lesional injection can be performed. Injection into a biopsy cavity, seroma, or hematoma may result in poor or no migration [3] and is not recommended. Prior to surgical biopsy, 1% isosulfan blue dye is also commonly injected around the margins of the tumor (intraparenchymal) in order to aid in SLN localization. The combination of isotope and blue dye have a complementary effect in sentinel node localization [10-12,14,18].

1- Intraparenchymal/peritumoral injection: It would seem logical that a peri-tumoral injection of the tracer would most accurately reflect the lymphatic drainage of the lesion [11]. Approximately 0.5 - 1.0 mCi of the agent in a total volume of 3 to 7 ml is injected in 4 to 6 deposits around the periphery of the tumor [3,18]. If the lesion is not palpable, a single injection can be performed through a localizing wire introducing needle [5] or using ultrasound guidance. A peri-tumoral injection will generally have slower tracer clearance than an intradermal exam- especially in patients with large breasts or post-menopausal women (possibly due to reduced lympahtic flow in the aging breast parenchyma) [18]. Images are usually obtained 45 minutes to 1-2 hours after injection [28]. A gentle massage for 2-3 minutes after the injection may aid clearance [18]. Due to the several injections made with this technique, there may be a "blooming" of the tracer activity which can obscure the axilla or internal mammary node area on imaging [11]. Some authors also report a decrease in SLN identification with this technique compared to an intradermal injection [11,17], however, there is a high rate of visualization of internal mammary sentinel nodes [18]. If visualization of internal mammary lymph nodes is deemed important, then a peritormal injection should be performed [28]. Some sentinel nodes can also be identified in the breast parenchyma, in between the pectoralis muscles, and in the supraclavicular fossa [18].

2- Intra/subdermal injection: Because of its embryologic origin in the ectoderm, the mammary gland is an organ of the skin and its lymphatic drainage mostly parallels lymph flow from the overlying skin [18]. For the dermal injection technique, a single injection of the tracer is made in the skin directly overlying the tumor [18]. Dermal injections are generally performed using a smaller dose and volume (0.1 to 0.6 mCi in 0.15 to 0.5 mL) [9,18]. The lower injected activity is associated with less "blooming" and the technique is easier to perform than peri-tumoral injections [11,14]. Tracer migration is also faster using a dermal injection with visualization of the sentinel node as early as 20-30 minutes following injection [16,18]. Localization of the SLN with this technique is excellent [10,11,14] and a dermal injection may actually be superior to a peri-tumoral injection for SLN identification [11,15]. A potential drawback of dermal injections is that they may be less likely to drain toward the deep fascial lymphatic channels and have a lower detection of intramammary nodes (i.e.: non-axillary sentinel nodes) [16-18]. The incidence of metastatic involvement of internal mammary nodes in patients with T1 (up to 2 cm diameter) breast cancer has been reported to be as high as 15%, but a much lower value has also been reported (about 3%) [18]. A reasonable approach might be to inject the radiocolloid intradermally when evaluating a T1a-b tumor (less than or equal to 1 cm in diameter) located superficially in the breast, and inject peritumorally in the case of larger tumors or tumors located deep within the breast [18]. A combination of peritumoral and intradermal injections can also be performed [28].

3- A single intratumoral injection is an alternative method and is also a valid way to identify the lymphatic drainage from the lesion [6]. There are several drawbacks to an intratumoral injection. The tumor itself is intrinsically devoid of an organized lymphatic system and drainage is often very slow [18]. Even 18-24 hours after injection, a large fraction of the injected dose is retained within the tumor [18]. Scatter or shine-through associated with this retained activity can interfere with imaging and gamma-probe use during surgery [18]. Although rare, an intratumoral injection could also spread tumor cells along the needle track [18].

4- Periareolar region injection: In the breast, there is a rich subareolar lymphatic plexus (the plexus of Sappey) [29]. Injections are performed adjacent to the areola in the tumor quadrant [28]. Activity reaches the axilla at a similar or faster rate than for dermal injections [28]. However, with the use of periareolar injections, there is less "shine-though" of activity which can sometimes interfere with the exam- particularly when injections are made in the upper-outer quadrant of the breast [29]. The sentinel lymph node detection rate is about 98% [29]. As with other superficial injection techniques, detection of drainage to internal mammary lymph nodes is decreased when compared to peritumoral injections [29].

Imaging:

A large-field-of-view camera is useful to obtain the draining pattern of the entire lymphatic basin [18]. The energy setting of the camera should be centered on the 140-keV emission peak of Tc-99m, with a +/- 10% window. The use of a high-resolution collimator and an acquisition matrix of 256x256 is recommended [18]. Imaging should begin within a few minutes of injection, however, dynamic imaging is not required as it is for sentinel node localization in melanoma [16]. The patient should be placed in a supine/semirecumbent position with the ipsilateral shoulder elevated to about 45 degrees by a triangular foam wedge and the arm raised over the head. This position helps to separate injection activity from axillary node activity [7] and allows the head of the gamma camera to be placed as close as possible to the axilla [18]. In patients with large breasts, it is sometimes useful to move the breast to clear the axillary region and reduce the attenuation effect [18]. Imaging is started with an anterior projection, but can be changed to an oblique anterior view with some craniocaudal tilting as necessary to distinguish between injection and nodal activity [18]. At completion of the exam an anterior image is still useful to obtain for evaluation of activity in the internal mammary nodes [7]. Nodes located close to the injection site may sometimes be obscured by scatter radiation. Adjusting the energy window to sample only the high side of the technetium photopeak can assist in identifying these nodes (ie: use 15% energy window centered at 151 keV) [3]. Timing of the sequential spot images should be based upon the size of the colloid particles injected and the type of injection used (peritumoral vs intradermal) [18]. The mean time to visualization of the sentinel node is about 20 minutes [3], but imaging can take up to 2 hours. An outline of the patients silhouette traced with a Tc-99m point source (< 0.5 mCi) or with a Co-57 sheet source behind the patient aids in image interpretation [3,18].

Once identified, the sentinel node should be further localized and marked on the skin with an indelible marker using a hand-held probe with the patient in the same position that will be used in surgery (generally the arm should be abducted to 90 degrees [18]). Marking the approximate position of the sentinel node may assist the surgeon in reducing operating time and in keep the surgical incision to a minimum [18]. If imaging is delayed, multiple nodes may be seen and localization of the sentinel node may not be possible. If a sentinel node is not identified on scintigraphic imaging, a sentinel node can still often times be localized at surgery- either with a handheld probe or with blue dye [10]. However, in patients that fail to have a sentinel node identified during imaging, there is a higher rate of failure to identify a SLN at surgery (19% of patients with non-visualized SLN on imaging had no SLN identified at surgery, as compared to only 1% of patients with visualized SLN at imaging) [10]. Patients over the age of 50-60 years are also more likely to have failure to localize the sentinel node [10,11].

A two day protocol has also been evaluated using unfiltered Tc-sulfurcolloid with results similar to the one day exam (sensitivity for sentinel node localization was 97%) [9]. This protocol permits greater flexibility for patients and operating room time is not wasted waiting for patients to arrive from lymphoscintigraphy [9]. A higher dose of Tc-sulfurcolloid is used (0.5 mCi or 18.5 MBq) to allow for radioactive decay of the agent.

Sentinel lymph node imaging: The lymphoscintigraphy exam below was performed using a peri-tumoral tracer injection. Images were performed at 5, 10, and 15 minutes after injection in a LAO projection with the left arm behind the patient's head. A lead shield was placed over the breast. The exam demonstrated rapid localization of the primary lymphatic drainage to the axilla. Following the procedure the patient went to the operating room for gamma probe localization of the sentinel node.

At surgery, a hand-held gamma probe is used to localize the sentinel node. The count rate in the sentinel node should be at least 3 to 5 times axillary background [5,9,15]. Often, surgeons will also pre-operatively (5 to 10 minutes before axillary dissection) inject 1% isosulfan blue dye around the tumor site to aid in the visual identification of the sentinel node and lymphatic drainage. Blue due localization is complementary to lymphoscintigraphy and can identify a small percentage of sentinel nodes (3.5-11%) not found by isotope localization [9,15]. Following removal of the sentinel node the operative site should be re-examined to ensure that the area of radioactivity has been removed and that a second node is not also active [18]. More than one sentinel node is found in a relevant number of patients (generally 1.5-1.8 per patient) [18]. All radioactive nodes should be excised until no areas of increased counts are found [18]. Gamma probe localization without lymphscinitgraphy imaging may be adequate for sentinal node localization [4,10]. However, images often help the surgeon by demonstrating the location and number of sentinel nodes, as well as unusual secondary routes of lymphatic drainage [24,26]. Additionally, visualization of sentinel lymph nodes at lymphoscintigraphy is predictive of a technically successful sentinel node biopsy procedure [24].

Failure to identify the sentinel node is an indication for standard axillary dissection [3] as lack of identification of this node does not exclude the presence of axillary metastases [10]. Meticulous intraoperative frozen section histopathologic analysis is performed on the node with the highest count rate, as well as on any additional lymph nodes with counting rates at least 20% of the count rate in the hottest node [18]. 

Dosimetry:

It is important to establish procedures for handling/processing specimens, monitoring personnel, and monitoring work areas for radiation for lymphoscintigraphic localizations [3]. The dose to the breast tissue is estimated to be approximately 45 rads per mCi of Tc-99m-sulfer colloid (1.2 cGy/MBq) assuming a distribution of the injected dose in 6 cc of tissue [3]. The estimate can vary by an order of magnitude depending on the volume of distribution and washout rate [3]. For peritumoral injections, resection of the breast tumor during surgery will help to decrease the radiation burden [3]. The amount of radioactivity actually retained in the sentinel node is about 1% of the injected dose (subdermal injection) [18]. The surgeon receives a hand dose of about 9.4 +/- 3.6 mrem per case [3]. The cumulative dose to personnel involved in the procedure (surgeons, nurses, pathologists) for 100 operations is at most about 1% (mean absorbed dose) or about 10% (mean effective dose) of the annual dose limits for the general population [18]. The radioactivity counted in the oeprating room material possibly contaminated during surgery is generally minimal and special handling procedures are not required [18]. The simple precaution of letting radioactivity decay for some hours is sufficient for tissue specimens in the pathology department [18],

Conclusion:

Sentinel node localization is a team effort that requires close coordination between the surgical team, radiology and nuclear medicine. The surgeon and nuclear medicine physician should have a clear understanding regarding the meaning of skin marks, patient position, and sources of artifacts [3]. The use of both a blue dye and radioscinitgraphy will give the benefit of visual cues and count-rate data for the surgeon [3,4]. A learning curve exists, and success improves with experience [4]. Each institution must set up a program with strict technical guidelines to confirm the accuracy of the examination [12]. The American Society of Breast Surgeons recommends that surgeons anticipating the use of sentinel node biopsy as their sole means of staging the axilla should first perform 30 validation cases with accurate identification of the sentinel node 85% of the time and a false-negative rate less than or equal to 5% [13].

REFERENCES:
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(2) J Nucl Med 1998; De Cicco C, et al. Lymphoscintigraphy and radioguided biopsy of the sentinel axillary node in breast cancer. 39: 2080-2084

(3) Semin Nucl Med 1999; Glass EC, et al. Sentinel node localization in breast cancer. 29 (1): 57-68

(4) Radiology 1999; Liberman L, et al. Sentinel lymph node biopsy after percutaneous diagnosis of nonpalpable breast cancer. 211: 835-844

(5) Radiology 1999; Eary JF, et al. Sentinel lymph node mapping for breast cancer: Analysis in a diverse patient group. 213: 526-529

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(7) J Nucl Med 2000; Haigh PI, et al. Factors affecting sentinel node localization during preoperative breast lymphscintigraphy. 41: 1682-1688

(8) AJR 2001; Tuthill LL, et al. Biopsy of sentinel lymph nodes guided by lymphoscintigraphic mapping in patients with breast cancer. 176: 407-411

(9) J Nucl Med 2001; Yeung HW, et al. Lymphoscintigraphy and sentinel onde localization in breast cancer patients: A comparison between 1-day and 2-day protocol. 42: 420-423

(10) Radiology 2001; Birdwell RL, et al. Breast cancer. Variables affecting sentinel lymph node visualization at preoperative lymphscintigraphy. 220: 47-53

(11) Ann Surg Oncol 1999; Linehan DC, et al. Intradermal radiocolloid and intraparenchymal blue dye injection optimized sentinel node identification in breast cancer patients. 6: 450-454

(12) Ann Surg Oncol 2001; Grube BJ, Giuliano AE. Modification of the sentinel node technique: It was a hit in New York, but will it play in Poughkeepsie? 8: 3-6 (No abstract available)

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(14) Ann Surg Oncol 2001; Boolbol SK, et al. Intradermal isotope injection: A highly accurate method of lymphatic mapping in breast carcinoma. 8: 20-24

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(16) Society of Nuclear Medicine Annual Meeting Handout Book 2001; Keshtgar MRS, et al. The sentinel node in breast carcinoma- present controversies. 80-92 (No abstract available)

(17) Eur J Nucl Med 2001; Nieweg OE, et al. Summary of the second international sentinel node conference. 28: 646-649 (No abstract available)

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(19) Radiographics 2002; Eubank WB, et al. Detection of locoregional and distant recurrences in breast cancer patients using FDG PET. 22: 5-17

(20) AJR 2002; Moshiri M, et al. Using lymphoscintigraphy to evaluate suspected lymphedema of the extremities. 178: 405-412 (No abstract available)

(21) J Nucl Med 2002; Mariani G, et al. Radioguided sentinel lymph node biopsy in malignant cutaneous melanoma. 43: 811-827

(22) J Nucl Med 2003; Kumar R, et al. Retrospective analysis of sentinel node localization in multifocal, multicentric, palpable or nonpalpable breast cancer. 44: 7-10

(23) J Nucl Med 2003; Szuba A, et al. The third circulation: radionuclide lymphoscintigraphy in the evaluation of lymphedema. 44: 43-57

(24) Radiology 2003; Liberman L. Lymphoscintigraphy for lymphatic mapping breast carcinoma. 228: 313-315

(25) Radiology 2003; Tanis PJ, et al. Lymphatic mapping in patients with breast carcinoma: reproducibility of lymphoscintigraphic results. 228: 546-551

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