J Neurol Surg B Skull Base 2018; 79(03): 282-288
DOI: 10.1055/s-0037-1607288
Original Article
Georg Thieme Verlag KG Stuttgart · New York

Rates and Locations of Regional Metastases in Sinonasal Malignancies: The Mayo Clinic Experience

Brandon W. Peck
1   Department of Otorhinolaryngology, Mayo Clinic, Rochester, Minnesota, United States
,
Kathryn M. Van Abel
1   Department of Otorhinolaryngology, Mayo Clinic, Rochester, Minnesota, United States
,
Eric J. Moore
1   Department of Otorhinolaryngology, Mayo Clinic, Rochester, Minnesota, United States
,
Daniel L. Price
1   Department of Otorhinolaryngology, Mayo Clinic, Rochester, Minnesota, United States
› Author Affiliations
Further Information

Publication History

28 February 2017

04 September 2017

Publication Date:
01 November 2017 (online)

Abstract

Objectives The objective of this study was to identify factors that may influence the rate and location of regional metastasis in sinonasal malignancies (SNMs).

Design This is a retrospective review.

Setting This study was set at the single-institution tertiary referral center.

Participants A total of 299 patients were treated for SNMs from 1994 to 2014.

Main Outcome Measures The main outcome measures were incidence and distribution of regional metastases.

Results Several histologic subtypes were treated, with squamous cell carcinoma (28.4%), esthesioneuroblastoma (18.1%), and mucosal melanoma (12.4%) being the most common. Of the 299 patients, 59 (19.7%) developed a regional metastasis, either at presentation or during follow-up. Higher cumulative incidence of regional metastases was significantly associated with histologic type (p ≤0.001) and invasion of the dura (p = 0.005), infratemporal fossa (p = 0.036), orbit (p = 0.020), or palate (p = 0.016). Ipsilateral level II lymph nodes were the most commonly involved nodes. Contralateral regional metastases were associated with higher risk histologic types (p = 0.005) and dural invasion (p = 0.008). Parotid metastases were associated with invasion of the facial soft tissue (p = 0.028), and retropharyngeal metastases were associated with invasion of the pterygoid plates and musculature (p = 0.030).

Conclusion Histologic type of SNM appears to be the most important factor in predicting the rate of regional metastases. Histologic type and invasion of certain neighboring structures may help define which lymphatic basins are at highest risk for metastasis.

Level of Evidence

The level of evidence is Level IV—retrospective case series.


Financial Support

This research was supported by departmental funding.


 
  • References

  • 1 Turner JH, Reh DD. Incidence and survival in patients with sinonasal cancer: a historical analysis of population-based data. Head Neck 2012; 34 (06) 877-885
  • 2 Dutta R, Dubal PM, Svider PF, Liu JK, Baredes S, Eloy JA. Sinonasal malignancies: a population-based analysis of site-specific incidence and survival. Laryngoscope 2015; 125 (11) 2491-2497
  • 3 Dulguerov P, Jacobsen MS, Allal AS, Lehmann W, Calcaterra T. Nasal and paranasal sinus carcinoma: are we making progress? A series of 220 patients and a systematic review. Cancer 2001; 92 (12) 3012-3029
  • 4 Dubal PM, Bhojwani A, Patel TD. , et al. Squamous cell carcinoma of the maxillary sinus: a population-based analysis. Laryngoscope 2016; 126 (02) 399-404
  • 5 Guan X, Wang X, Liu Y, Hu C, Zhu G. Lymph node metastasis in sinonasal squamous cell carcinoma treated with IMRT/3D-CRT. Oral Oncol 2013; 49 (01) 60-65
  • 6 Mirghani H, Hartl D, Mortuaire G. , et al. Nodal recurrence of sinonasal cancer: does the risk of cervical relapse justify a prophylactic neck treatment?. Oral Oncol 2013; 49 (04) 374-380
  • 7 Jiang GL, Ang KK, Peters LJ, Wendt CD, Oswald MJ, Goepfert H. Maxillary sinus carcinomas: natural history and results of postoperative radiotherapy. Radiother Oncol 1991; 21 (03) 193-200
  • 8 Kim GE, Chung EJ, Lim JJ. , et al. Clinical significance of neck node metastasis in squamous cell carcinoma of the maxillary antrum. Am J Otolaryngol 1999; 20 (06) 383-390
  • 9 Gooley TA, Leisenring W, Crowley J, Storer BE. Estimation of failure probabilities in the presence of competing risks: new representations of old estimators. Stat Med 1999; 18 (06) 695-706
  • 10 Gray RJ. A class of K-sample tests for comparing the cumulative incidence of a competing risk. Ann Stat 1988; 16 (03) 1141-1154
  • 11 Cantù G, Bimbi G, Miceli R. , et al. Lymph node metastases in malignant tumors of the paranasal sinuses: prognostic value and treatment. Arch Otolaryngol Head Neck Surg 2008; 134 (02) 170-177
  • 12 Unsal AA, Dubal PM, Patel TD. , et al. Squamous cell carcinoma of the nasal cavity: a population-based analysis. Laryngoscope 2016; 126 (03) 560-565
  • 13 Aspelund A, Antila S, Proulx ST. , et al. A dural lymphatic vascular system that drains brain interstitial fluid and macromolecules. J Exp Med 2015; 212 (07) 991-999
  • 14 Louveau A, Smirnov I, Keyes TJ. , et al. Structural and functional features of central nervous system lymphatic vessels. Nature 2015; 523 (7560): 337-341
  • 15 Rouviere H. Anatomie Des Lymphatiques de L'homme. Paris: Masson et cie; 1932
  • 16 Fernández JM, Santaolalla F, Del Rey AS, Martínez-Ibargüen A, González A, Iriarte MR. Preliminary study of the lymphatic drainage system of the nose and paranasal sinuses and its role in detection of sentinel metastatic nodes. Acta Otolaryngol 2005; 125 (05) 566-570
  • 17 Shidnia H, Hornback NB, Saghafi N, Sayoc E, Lingeman R, Hamaker R. The role of radiation therapy in the treatment of malignant tumors of the paranasal sinuses. Laryngoscope 1984; 94 (01) 102-106
  • 18 Katz TS, Mendenhall WM, Morris CG, Amdur RJ, Hinerman RW, Villaret DB. Malignant tumors of the nasal cavity and paranasal sinuses. Head Neck 2002; 24 (09) 821-829