This article has Open Peer Review reports available.
How we do it: a method of neck dissection for histopathological analysis
© Upile et al; licensee BioMed Central Ltd. 2007
Received: 25 June 2007
Accepted: 31 October 2007
Published: 31 October 2007
Dissection of the lymphatic structures in the neck is an integral part of the management of many head and neck cancers.
We describe a technique of surgical dissection, preparing the tissue for more precise histological analysis while also reducing operative time and complexity.
When dissected, each level is excised between lymph nodes groups and put into a separate pot of formalin taking care to avoid rupture of any obvious pathological nodes.
This makes for a simpler dissection as the surgeon progresses, as a larger more cumbersome specimen is avoided and manipulation of involved nodes is actually reduced with a reduced risk of tumour spillage.
We feel that our technique provides several advantages for the histopathologist as well as the surgeon. As the dissection of the specimen into the relevant levels has already been performed, time is saved in orientating and then dissecting the specimen. Accuracy of dissection is also improved and each piece of tissue is a more manageable size for processing and analysis.
This technique may also have several surgical advantages when compared with the commonly practiced techniques e.g. with reducing in-vivo specimen manipulation, hence reducing the risk of inadvertent injury to important structures and tumour spillage.
A neck dissection specimen when removed "en bloc" (radical neck dissection) and preserved in formalin may be unrecognisable when processed by the histopathology laboratory. Even when labelled or pinned on cork board (orientation plate), the boundaries of the levels of lymph nodes within the neck are surgical boundaries not easy to delineated in the resected specimen. Considering that up to 30% formalin-related post-excision shrinkage may occur, any labelling technique has to be able to withstand the vagaries of processing.
This is more so with the increasing use of the modified radical (selective) neck dissection were preservation of the internal jugular vein and the sternocleidomastiod (SCM) and functional neck dissection further increase the difficulty of orientating the specimen.
Correct and accurate analysis of the lymph nodes surgically excised in a head and neck cancer case is extremely important for the prognostic, diagnostic and treatment information it provides. In the situation of an occult primary, the level of lymph node metastasis will give a clue to the site of origin of disease. Also as increasing levels or more distant levels are affected by disease, so prognosis worsens [1, 2].
In a study involving 20 cadaver neck dissections, a quantification of lymph nodes in selective neck dissection took place. The average number of lymph nodes removed for levels I–V was 24, with 13 for levels I–III and 19 for levels II–IV, when compared to other clinical reviews; Friedman et al. concluded that the number of lymph nodes removed in selective neck dissection should be comparable to that of the corresponding levels in radical neck dissection, provided that strict adherence to surgical boundaries is maintained .
We describe a technique of level-specific neck dissection in which each level of lymph nodes are dissected separately, and sent for histological analysis separately. This improves the accuracy of the resection as the boundaries of the levels are seen and used at surgery and not arbitrarily taken in the lab. It also shortens the resection time.
Methods and Results
Surgical Levels of the head & Neck
Lower border of the body of the mandible superiorly, posterior belly of the diagastric muscle posteriorly, hyoid bone inferiorly and the midline medially
Base of skull superiorly, lateral limit of the sternohyoid muscle anteriorly, posterior border of the sternocleidomastoid muscle posteriorly, and level of the hyoid bone inferiorly
Level of the hyoid bone superiorly, lateral limit of the sternohyoid muscle anteriorly, the posterior border of sternocleidomastoid muscle posteriorly, and the omohyoid tendon inferiorly
Omohyoid tendon superiorly, lateral limit of the sternohyoid muscle anteriorly, posterior border of the sternocleidomastoid muscle posteriorly, and clavicle inferiorly
Posterior border of sternocleidomastoid muscle anteriorly, anterior border of the trapezius muscle posteriorly, and clavicle inferiorly
In the laboratory the Pathologist cuts the tissue from each pot into pieces that will fit into the cassettes used routinely for histological processing into paraffin wax blocks. Often one tissue piece is bisected and processed in two blocks. This means one lymph node may cut in half and each half processed in a separate block. The block details are recorded so that one lymph node is not counted twice. Individual lymph nodes are not separated out from surrounding connective tissue but are identified at microscopy. Usually all of the tissue is processed from levels 3–5 however, salivary gland tissue often present in levels 1 & 2 tissue may be dissected and sampled and not all processed. Fibro-fatty tissue which often contains lymph nodes is all processed where possible. Sections 3–4 microns thick are cut from the paraffin blocks and usually one section per tissue block processed on a slide. Where the tissue blocks are small, more that one section may be present on a slide. Serial sections at different levels through the block are not routinely requested as this workload would not be sustainable in the routine laboratory. The sections are stained with haematoxylin and eosin. Immunostains for cytokeratin to detect micrometastases are not routinely requested.
The surgeon's responsibility does not end with just taking the excision specimen. A council of perfection would suggest that even before surgery a sampling strategy would be discussed with the pathologist including the location and possibility of any difficult areas and likely positive margins. The caveat is that further information may become available at surgery that may modify this strategy. Thus allowing adequate and appropriate resource allocation e.g. frozen section facility...etc.
In mitigation of a selective neck dissection, Muzaffar K conducted a retrospective, 25-year, study involving patients with untreated head and neck cancer who had squamous cell carcinoma (SCC) metastatic to cervical lymph nodes on histological examination and were treated with a selective, modified, or radical neck dissection. Evidence of recurrence was 3.3% in the selective neck dissection group and 5.2% in the radical and modified neck dissection group. Disease-free (2-year survival) was 80% in the selective neck dissection group and 64% in the radical and modified neck dissection group .
However, advanced nodal involvement can sometimes justify a more aggressive resection technique. Schiff et al. concluded that a selective neck dissection may be sufficient for many N+ patients with SCC, but some patients with extensive nodal disease may benefit from more aggressive treatment of the neck .
Jaehne et al. evaluated whether intra-operative macroscopic inspection of the sternocleidomastoid muscle in regard to tumour infiltration is sufficient to decide about muscle resection and whether there are prognostic differences between patients undergoing radical versus modified radical (selective) neck dissection. In a study involving 337 patients, they concluded that intraoperative inspection of the SCM constitutes a valid parameter for deciding whether tumour infiltration is present or not and there were no statistically significant prognostic differences (2-year, 5-year and 10-year-survival) between stage III and IV patients with oral cavity, oropharyngeal, hypopharyngeal and laryngeal carcinomas treated by either radical or selective neck dissection .
We have already discussed the erroneous assumption of the superiority of the naked eye "en-bloc" dissection over "selective" dissection between the nodes groups without node rupture . This is due in part upon the "en-bloc" enthusiasts mis-appreciation of true microscopic disease spread (via microlymphatics) and the tendency for many resections to reflect surgical ease or expediance despite their scope or duration . By answering this basic criticism of "selective" neck dissection we logically extend this rationale to histopathological sampling.
The problem we aim to resolve is that of perioperative co-registration of pathology with anatomy. Unfortunately, the classification of cervical lymph node levels also differ from those suggested by pre-operative radiological imaging, however this accuracy is related to neck level being imaged. This also has important implications for the anatomico-pathological accuracy of radiologically directed biopsy (Fine Needle Aspiration and if oncologically justified core biopsy). Since this may lead to errors in the pre-operative planning of the correct selective neck dissection carried out by the surgeon with consequent increase in locoregional recurrence or residual disease.
The presence of cervical nodal metastatses in head and neck cancer and the increasing number of levels involved worsens the prognosis . Determining the degree of nodal spread is important in firstly eradicating the disease and secondly in the decision regarding the use of postoperative treatment e.g. radiotherapy. With new techniques of delivery of radiotherapy such as intensity modulated radiotherapy , in which a radical treatment dose can be selectively applied to the involved nodal level, uninvolved levels and normal tissues can be spared reducing the associated morbidity of radical radiotherapy. It is imperative that there is accurate and reproducible co-registration of disease and in situ lymph node level. This is important considering the surgically directed brachytherapy treatment range (~1 cm) which spares more distant tissues from radiation toxicity. This ensures better dose delivery and may account for some of the variations in survival rates.
Bhattacharyya N found that the modified radical neck dissection and functional neck dissection, when compared with radical neck dissection, do not compromise the quantity of cervical nodes excised .
Accurate histological analysis of the resected specimen is therefore mandatory in managing these patients. Labelling techniques of neck dissection specimens have been described previously [10, 11], which can aid the histo-pathologist. However, we feel that our technique provides several advantages for the histo-pathologist as well as the surgeon. As the dissection of the specimen into the relevant levels has already been performed, time is saved in orientating and then dissecting the specimen. Accuracy of dissection is also improved and each piece of tissue is a more manageable size for processing and analysis.
This technique may have several surgical advantages when compared with the commonly practiced techniques. In a comprehensive neck dissection in which preservation of both the accessory nerve and internal jugular vein are goals, both of these structures are skeletonised and in doing this with a bulky cumbersome specimen which needs constant manipulation, there is increased risk of inadvertent injury to these structures and tumour spillage.
Furthermore, as illustrated in Figure 3 the actual three-dimensional bulk of the tumour cannot be encompassed by the standard two dimensional anatomical template upon which the neck dissection is secured. It is again the responsibility of the operating surgeon to take the knife and define the exact surgical borders of neck dissection levels rather than merely indicating a proxy.
- Kowalski LP, Bagietto R, Lara JR, Santos RL, Silva JF, Magrin J: Prognostic significance of the distribution of neck node metastasis from oral carcinoma. Head Neck. 2000, 22 (3): 207-14. 10.1002/(SICI)1097-0347(200005)22:3<207::AID-HED1>3.0.CO;2-9.View ArticlePubMedGoogle Scholar
- Upile T, Fisher C, Jerjes W, El Maaytah M, Searle A, Archer D, Michael's L, Rhys-Evans P, Hopper C, Howard D, Wright A: The uncertainty of the surgical margin in the treatment of head and neck cancer. Oral Oncol. 2007, 43 (4): 321-326. 10.1016/j.oraloncology.2006.08.002.View ArticlePubMedGoogle Scholar
- Friedman M, Lim JW, Dickey W, Tanyeri H, Kirshenbaum GL, Phadke DM, Caldarelli D: Quantification of lymph nodes in selective neck dissection. Laryngoscope. 1999, 109 (3): 368-70. 10.1097/00005537-199903000-00005.View ArticlePubMedGoogle Scholar
- Shaw H: A modification of the Mac Fee incisions for neck dissection. J Laryngol Otol. 1988, 102: 1124-1126.View ArticlePubMedGoogle Scholar
- Muzaffar K: Therapeutic selective neck dissection: a 25-year review. Laryngoscope. 2003, 113 (9): 1460-5. 10.1097/00005537-200309000-00005.View ArticlePubMedGoogle Scholar
- Schiff BA, Roberts DB, El-Naggar A, Garden AS, Myers JN: Selective vs modified radical neck dissection and postoperative radiotherapy vs observation in the treatment of squamous cell carcinoma of the oral tongue. Arch Otolaryngol Head Neck Surg. 2005, 131 (10): 874-8. 10.1001/archotol.131.10.874.View ArticlePubMedGoogle Scholar
- Jaehne M, Ussmuller J, Kehrl W: Resection of the sternocleidomastoid muscle during radical neck dissection. Eur Arch Otorhinolaryngol. 2001, 258 (4): 192-7. 10.1007/s004050100337.View ArticlePubMedGoogle Scholar
- Nutting C, Dearnaley DP, Webb S: Intensity modulated radiation therapy: a clinical review. Br J Radiol. 2000, 73: 459-469.View ArticlePubMedGoogle Scholar
- Bhattacharyya N: The effects of more conservative neck dissections and radiotherapy on nodal yields from the neck. Arch Otolaryngol Head Neck Surg. 1998, 124 (4): 412-6.View ArticlePubMedGoogle Scholar
- Rhys-Evans PH, Morgan D, Smallman L: Preservation of neck dissection for histological study. J Laryngol Otol. 1987, 101: 823-827.View ArticlePubMedGoogle Scholar
- Winter SC, Corbridge R, Shah K, Millard P, Cox GJ: Orientation and labelling: use of an acetate sheet to label tumour resection specimens. Ann R Coll Surg Eng. 2003, 85: 62-3. 10.1308/14736350360507415.View ArticleGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2482/7/21/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.