Skip to main content

Advertisement

Log in

Discordance in Histopathologic Evaluation of Melanoma Sentinel Lymph Node Biopsy with Clinical Follow-Up: Results from a Prospectively Collected Database

  • Melanomas
  • Published:
Annals of Surgical Oncology Aims and scope Submit manuscript

Abstract

Background

Sentinel lymph node (SLN) status currently represents the single most important prognostic factor in clinically localized melanoma and is widely used in patients with melanoma at significant risk for nodal micrometastasis. Although several studies have looked at the rates and implications of inaccuracies in the histopathologic diagnosis of melanocytic lesions, accuracy in the histologic interpretation of the SLN in melanoma has not been addressed. The goal of this study was to determine the rates of discordance in the histopathologic evaluation of the SLN and the potential clinical impact on patients referred to a comprehensive melanoma center.

Methods

A prospectively collected database was queried for melanoma patients who had SLN biopsies performed at outside institutions before referral to the University of Michigan Multidisciplinary Melanoma Program between 2006 and 2009. These cases were reviewed and clinical follow-up obtained.

Results

After internal review of the SLN material, 13 (8 %) of 167 cases had major discrepancies in diagnosis that impacted patient management and prognosis. The disease of five patients was subsequently downstaged and the disease of eight patients was upstaged after internal review of the SLNs and reversal in diagnoses.

Conclusions

There appears to be a small yet significant rate of discordance in diagnosis of the SLN for melanoma after expert histopathologic review. The implications of this discordance and revision of diagnosis is substantial. Expert histopathologic review of the SLN warrants consideration to provide the most accurate prognostic information and optimal patient care.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Balch CM, Gershenwald JE, Soong SJ, et al. Final version of 2009 AJCC melanoma staging and classification. J Clin Oncol. 2009;27:6199–206.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Balch CM, Gershenwald JE, Soong SJ, et al. Multivariate analysis of prognostic factors among 2,313 patients with stage III melanoma: comparison of nodal micrometastases versus macrometastases. J Clin Oncol. 2010;28:2452–9.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Balch CM, Gershenwald JE, Soong SJ, Thompson JF. Update on the melanoma staging system: the importance of sentinel node staging and primary tumor mitotic rate. J Surg Oncol. 2011;104:379–85.

    Article  PubMed  Google Scholar 

  4. Wong SL, Balch CM, Hurley P, et al. Sentinel lymph node biopsy for melanoma: American Society of Clinical Oncology and Society of Surgical Oncology joint clinical practice guideline. Ann Surg Oncol. 2012;19:3313–24.

    Article  PubMed  Google Scholar 

  5. Lodha S, Saggar S, Celebi JT, Silvers DN. Discordance in the histopathologic diagnosis of difficult melanocytic neoplasms in the clinical setting. J Cutan Pathol. 2008;35:349–52.

    Article  PubMed  Google Scholar 

  6. Scolyer RA, Shaw HM, Thompson JF, et al. Interobserver reproducibility of histopathologic prognostic variables in primary cutaneous melanomas. Am J Surg Pathol. 2003;27:1571–6.

    Article  PubMed  Google Scholar 

  7. van Dijk MC, Aben KK, van Hees F, et al. Expert review remains important in the histopathological diagnosis of cutaneous melanocytic lesions. Histopathology. 2008;52:139–46.

    Article  PubMed  Google Scholar 

  8. McGinnis KS, Lessin SR, Elder DE, et al. Pathology review of cases presenting to a multidisciplinary pigmented lesion clinic. Arch Dermatol. 2002;138:617–21.

    PubMed  Google Scholar 

  9. Santillan AA, Messina JL, Marzban SS, Crespo G, Sondak VK, Zager JS. Pathology review of thin melanoma and melanoma in situ in a multidisciplinary melanoma clinic: impact on treatment decisions. J Clin Oncol. 2010;28:481–6.

    Article  PubMed  Google Scholar 

  10. Shoo BA, Sagebiel RW, Kashani-Sabet M. Discordance in the histopathologic diagnosis of melanoma at a melanoma referral center. J Am Acad Dermatol. 2010;62:751–6.

    Article  PubMed  Google Scholar 

  11. Hawryluk EB, Sober AJ, Piris A, et al. Histologically challenging melanocytic tumors referred to a tertiary care pigmented lesion clinic. J Am Acad Dermatol. 2012;67:727–35.

    Article  PubMed  Google Scholar 

  12. Urist MM, Maddox WA, Kennedy JE, Balch CM. Patient risk factors and surgical morbidity after regional lymphadenectomy in 204 melanoma patients. Cancer. 1983;51:2152–6.

    Article  PubMed  CAS  Google Scholar 

  13. Murali R, Cochran AJ, Cook MG, et al. Interobserver reproducibility of histologic parameters of melanoma deposits in sentinel lymph nodes: implications for management of patients with melanoma. Cancer. 2009;115:5026–37.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Wong SL. Micrometastases in sentinel lymph nodes: not getting lost in translation. Ann Surg Oncol. 2012;19:1056–7.

    Article  PubMed  Google Scholar 

  15. Murali R, DeSilva C, McCarthy SW, Thompson JF, Scolyer RA. Sentinel lymph nodes containing very small (<0.1 mm) deposits of metastatic melanoma cannot be safely regarded as tumor-negative. Ann Surg Oncol. 2012;19:1089–99.

    Article  PubMed  Google Scholar 

  16. Scheri RP, Essner R, Turner RR, Ye X, Morton DL. Isolated tumor cells in the sentinel node affect long-term prognosis of patients with melanoma. Ann Surg Oncol. 2007;14:2861–6.

    Article  PubMed  Google Scholar 

  17. Gibbs JF, Huang PP, Zhang PJ, Kraybill WG, Cheney R. Accuracy of pathologic techniques for the diagnosis of metastatic melanoma in sentinel lymph nodes. Ann Surg Oncol. 1999;6:699–704.

    PubMed  CAS  Google Scholar 

  18. Spanknebel K, Coit DG, Bieligk SC, Gonen M, Rosai J, Klimstra DS. Characterization of micrometastatic disease in melanoma sentinel lymph nodes by enhanced pathology: recommendations for standardizing pathologic analysis. Am J Surg Pathol. 2005;29:305–17.

    Article  PubMed  Google Scholar 

  19. Lobo AZ, Tanabe KK, Luo S, et al. The distribution of microscopic melanoma metastases in sentinel lymph nodes: implications for pathology protocols. Am J Surg Pathol. 2012;36:1841–8.

    Article  PubMed  Google Scholar 

  20. Karimipour DJ, Lowe L, Su L, et al. Standard immunostains for melanoma in sentinel lymph node specimens: which ones are most useful? J Am Acad Dermatol. 2004;50:759–64.

    Article  PubMed  Google Scholar 

  21. Lohmann CM, Iversen K, Jungbluth AA, Berwick M, Busam KJ. Expression of melanocyte differentiation antigens and Ki-67 in nodal nevi and comparison of Ki-67 expression with metastatic melanoma. Am J Surg Pathol. 2002;26:1351–7.

    Article  PubMed  Google Scholar 

  22. Gray MH, Talbert ML, Talbert WM, Bansal M, Hsu A. Changes seen in lymph nodes draining the sites of large joint prostheses. Am J Surg Pathol. 1981;13:1050–6.

    Article  Google Scholar 

  23. Anderson LL, Cardone JS, McCollough ML, Grabski WJ. Tattoo pigment mimicking metastatic malignant melanoma. Dermatol Surg. 1996;22:92–4.

    PubMed  CAS  Google Scholar 

  24. Gould E, Porto R, Albores-Saavedra J, Ibe MJ. Dermatopathic lymphadenitis: the spectrum and significance of its morphologic features. Arch Pathol Lab Med. 1988;112:1145–50.

    PubMed  CAS  Google Scholar 

  25. Moehrle M, Blaheta HJ, Ruck P. Tattoo pigment mimics positive sentinel lymph node in melanoma. Dermatology. 2001;203:342–4.

    Article  PubMed  CAS  Google Scholar 

  26. Johnson TM, Chang A, Redman B, et al. Management of melanoma with a multidisciplinary melanoma clinic model. J Am Acad Dermatol. 2000;42:820–6.

    Article  PubMed  CAS  Google Scholar 

  27. Haws B, St Romain P, Mammen J, Fraga GR. Secondary review of external histopathology on cutaneous oncology patients referred for sentinel lymph node biopsy: how often does it occur and is it worth it? J Cutan Pathol. 2012;39:844–9.

    Article  PubMed  Google Scholar 

  28. Newman EA, Guest AB, Helvie MA, et al. Changes in surgical management resulting from case review at a breast cancer multidisciplinary tumor board. Cancer. 2006;107:2346–51.

    Article  PubMed  Google Scholar 

  29. Stevens WB, van Krieken JH, Mus RD, et al. Centralised multidisciplinary re-evaluation of diagnostic procedures in patients with newly diagnosed Hodgkin lymphoma. Ann Oncol. 2012;23:2676–81.

    Article  PubMed  CAS  Google Scholar 

  30. Li L, Scolyer RA, Ka V, et al. Pathologic review of negative sentinel lymph nodes in melanoma patients with regional recurrence: a clinicopathologic study of 1152 patients undergoing sentinel lymph node biopsy. Am J Surg Pathol. 2003;27:1197–202.

    Article  PubMed  Google Scholar 

  31. Carlson GW, Page AS, Cohen C, et al. Regional recurrence after negative sentinel lymph node biopsy for melanoma. Ann Surg. 2008;248:378–86.

    PubMed  Google Scholar 

Download references

Acknowledgment

We thank Nisha Meireles, Clinical Research Specialist, Multidisciplinary Melanoma Program, for database and data management.

Conflict of interest

The authors declare no conflict of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Rajiv M. Patel MD.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Dandekar, M., Lowe, L., Fullen, D.R. et al. Discordance in Histopathologic Evaluation of Melanoma Sentinel Lymph Node Biopsy with Clinical Follow-Up: Results from a Prospectively Collected Database . Ann Surg Oncol 21, 3406–3411 (2014). https://doi.org/10.1245/s10434-014-3773-8

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1245/s10434-014-3773-8

Keywords

Navigation