J Breast Cancer.  2016 Jun;19(2):191-198. 10.4048/jbc.2016.19.2.191.

Breast Magnetic Resonance Imaging for Assessment of Internal Mammary Lymph Node Status in Breast Cancer

Affiliations
  • 1Division of Radiology, Seoul St. Mary's Hospital, The Catholic University of Korea College of Medicine, Seoul, Korea. rad-ksh@catholic.ac.kr

Abstract

PURPOSE
The purpose of this study was to assess magnetic resonance imaging (MRI) features of malignant internal mammary lymph nodes (IMLNs) and benign IMLNs in breast cancer patients.
METHODS
From 2009 to 2014, the records of 85 patients with IMLNs were archived using MRI report data; 26 patients with small size (long axis diameter <5 mm) nodes were subsequently excluded. The current study evaluated internal mammary lymph nodes in 59 patients who underwent breast MRI for breast cancer staging and for posttherapy follow-up. All MRI findings were retrospectively evaluated. Malignancy was determined based on pathologic examination and positron emission tomography computed tomography findings. Independent t-tests, Mann-Whitney U tests, chi-square tests, and receiver operating characteristics (ROC) curve analysis were used.
RESULTS
Among MRI features, there were statistically significant differences between benign and malignant IMLN groups, in short axis length (3.6±1.3 vs. 8.2±2.9 mm, respectively), long axis length (8.1±2.4 vs. 14.5±4.8 mm, respectively), short/long axis ratio (0.45±0.10 vs. 0.59±0.17, respectively), absent fatty hilum (mean, 0% vs. 95%, respectively), and restricted diffusion (15.8% vs. 85.0%, respectively) (p<0.050). Multiplicity and location of intercostal spaces was not different between the two groups. Short axis length was the most discriminative variable for predicting metastatic nodes (area under the ROC curve, 0.951; threshold, 4 mm; sensitivity, 92.5%; specificity, 84.2%).
CONCLUSION
Conventional MRI and diffusion-weighted MRI are helpful to detect metastasis of internal mammary lymph nodes in breast cancer.

Keyword

Breast neoplasms; Lymph nodes; Magnetic resonance imaging; Neoplasm metastasis

MeSH Terms

Breast Neoplasms*
Breast*
Diffusion
Follow-Up Studies
Humans
Lymph Nodes*
Magnetic Resonance Imaging*
Neoplasm Metastasis
Positron-Emission Tomography
Retrospective Studies
ROC Curve
Sensitivity and Specificity

Figure

  • Figure 1 A 41-year-old woman with invasive ductal carcinoma in the left breast and malignant lymph node confirmed by core needle biopsy. (A) Axial fat suppressed contrast enhanced T1-weighted image reveals an internal mammary lymph node in the first intercostal space with short axis of 15 mm, long axis of 17 mm and loss of fatty hilum. (B) Diffusion weighted imaging shows a high-signal-intensity of lymph node (arrow). (C) Apparent diffusion coefficient map shows a low-signal-intensity (arrow). (D) Positron emission tomography computed tomography reveals presence of focal fluorodeoxyglucose uptake in the same location of left internal mammary lymph node with a maximum standardized uptake value of 5.6 (arrow).

  • Figure 2 A 48-year-old woman with invasive ductal carcinoma in the left breast and malignant lymph node classified due to increased fluorodeoxyglucose (FDG) uptake on positron emission tomography computed tomography (PET/CT). (A) Axial fat suppressed T1-weighted image reveals an internal mammary lymph node (arrow) in the third intercostal space with loss of fatty hilum. (B) Axial fat suppressed contrast enhanced T1-weighted image, the size of lymph node is short axis of 9 mm and long axis of 15 mm. (C) Diffusion weighted imaging shows a high-signal-intensity of lymph node (arrow). (D) Apparent diffusion coefficient map shows a low-signal-intensity (arrow). (E) Initial PET/CT reveals presence of focal FDG uptake in the same location of left internal mammary lymph node with a maximum standardized uptake value of 1.5 (arrow). (F) Four months later, there is a marked increased FDG uptake from 1.5 to 7.8 (arrow).

  • Figure 3 A 41-year-old woman with invasive ductal carcinoma in the left breast and benign lymph node confirmed by fine-needle aspiration and biopsy. (A) Axial fat suppressed T1-weighted image reveals an internal mammary lymph node (arrowheads) in the second intercostal space with preserved fatty hilum showing low-signal-intensity (arrow). (B) On axial fat suppressed contrast enhanced T1-weighted image, the size of lymph node is 4 mm (short axis) and 12 mm (long axis). (C) Diffusion weighted imaging shows a high-signal-intensity of lymph node (arrow). (D) Apparent diffusion coefficient map shows a iso-signal-intensity (arrow).

  • Figure 4 A 53-year-old woman with invasive ductal carcinoma in the left breast and benign lymph node (LN) classified due to no fluorodeoxyglucose (FDG) uptake on positron emission tomography computed tomography (PET/CT). (A) Axial fat suppressed contrast enhanced T1-weighted image reveals an internal mammary LN in the second intercostal space with short axis of 3 mm, long axis of 7 mm and preserved fatty hilum. (B) Diffusion weighted imaging shows a high-signal-intensity of LN (arrow). (C) Apparent diffusion coefficient map shows a low-signal-intensity (arrow). Initial (D) and after 1 year and 1 month (E) PET/CT reveals absence of focal FDG uptake in the same location of left internal mammary LN (arrow).

  • Figure 5 Receiver operating characteristic curves for the individual evaluated magnetic resonance imaging parameters of the internal mammary lymph node. The area under the receiver operating characteristics curve of short axis length, long axis length and short axis length/long axis length (S/L) ratio were 0.951, 0.906, and 0.756, respectively.


Reference

1. Li Z, Gu X, Tong J, Liu B, Sun L, Gao X, et al. A meta-analysis of internal mammary lymph node metastasis in breast cancer patients. Onkologie. 2013; 36:747–752.
Article
2. Cody HS 3rd. Clinical significance and management of extra-axillary sentinel lymph nodes: worthwhile or irrelevant? Surg Oncol Clin N Am. 2010; 19:507–517.
Article
3. Veronesi U, Marubini E, Mariani L, Valagussa P, Zucali R. The dissection of internal mammary nodes does not improve the survival of breast cancer patients: 30-year results of a randomised trial. Eur J Cancer. 1999; 35:1320–1325.
Article
4. Cranenbroek S, van der Sangen MJ, Kuijt GP, Voogd AC. Diagnosis, treatment and prognosis of internal mammary lymph node recurrence in breast cancer patients. Breast Cancer Res Treat. 2005; 89:271–275.
5. Maalej M, Gargouri W, Kochbati L, Nasr C, Frikha H, Hentati D, et al. Internal mammary lymph node invasion in breast cancer: myth or reality? Tunis Med. 2009; 87:319–322.
6. Noguchi M. Internal mammary sentinel node biopsy for breast cancer: is it practicable and relevant? (Review). Oncol Rep. 2002; 9:461–468.
Article
7. An YY, Kim SH, Kang BJ, Lee AW. Comparisons of positron emission tomography/computed tomography and ultrasound imaging for detection of internal mammary lymph node metastases in patients with breast cancer and pathologic correlation by ultrasound-guided biopsy procedures. J Ultrasound Med. 2015; 34:1385–1394.
Article
8. Chen RC, Lin NU, Golshan M, Harris JR, Bellon JR. Internal mammary nodes in breast cancer: diagnosis and implications for patient management: a systematic review. J Clin Oncol. 2008; 26:4981–4989.
Article
9. Kinoshita T, Odagiri K, Andoh K, Doiuchi T, Sugimura K, Shiotani S, et al. Evaluation of small internal mammary lymph node metastases in breast cancer by MRI. Radiat Med. 1999; 17:189–193.
10. Seo MJ, Lee JJ, Kim HO, Chae SY, Park SH, Ryu JS, et al. Detection of internal mammary lymph node metastasis with (18)F-fluorodeoxyglucose positron emission tomography/computed tomography in patients with stage III breast cancer. Eur J Nucl Med Mol Imaging. 2014; 41:438–445.
Article
11. Kim EJ, Kim SH, Kang BJ, Choi BG, Song BJ, Choi JJ. Diagnostic value of breast MRI for predicting metastatic axillary lymph nodes in breast cancer patients: diffusion-weighted MRI and conventional MRI. Magn Reson Imaging. 2014; 32:1230–1236.
Article
12. Mack M, Chetlen A, Liao J. Incidental internal mammary lymph nodes visualized on screening breast MRI. AJR Am J Roentgenol. 2015; 205:209–214.
Article
13. Ray KM, Munir R, Wisner DJ, Azziz A, Holland BC, Kornak J, et al. Internal mammary lymph nodes as incidental findings at screening breast MRI. Clin Imaging. 2015; 39:791–793.
Article
14. He N, Xie C, Wei W, Pan C, Wang W, Lv N, et al. A new, preoperative, MRI-based scoring system for diagnosing malignant axillary lymph nodes in women evaluated for breast cancer. Eur J Radiol. 2012; 81:2602–2612.
Article
15. Yoshimura G, Sakurai T, Oura S, Suzuma T, Tamaki T, Umemura T, et al. Evaluation of axillary lymph node status in breast cancer with MRI. Breast Cancer. 1999; 6:249–258.
Article
16. Luciani A, Dao TH, Lapeyre M, Schwarzinger M, Debaecque C, Lantieri L, et al. Simultaneous bilateral breast and high-resolution axillary MRI of patients with breast cancer: preliminary results. AJR Am J Roentgenol. 2004; 182:1059–1067.
Article
17. Mortellaro VE, Marshall J, Singer L, Hochwald SN, Chang M, Copeland EM, et al. Magnetic resonance imaging for axillary staging in patients with breast cancer. J Magn Reson Imaging. 2009; 30:309–312.
Article
18. Fornasa F, Nesoti MV, Bovo C, Bonavina MG. Diffusion-weighted magnetic resonance imaging in the characterization of axillary lymph nodes in patients with breast cancer. J Magn Reson Imaging. 2012; 36:858–864.
Article
19. Junping W, Tongguo S, Yunting Z, Chunshui Y, Renju B. Discrimination of axillary metastatic from nonmetastatic lymph nodes with PROPELLER diffusion-weighted MR imaging in a metastatic breast cancer model and its correlation with cellularity. J Magn Reson Imaging. 2012; 36:624–631.
Article
20. Wang J, Liao Q, Zhang Y, Yu C, Bai R, Sun H. Differential diagnosis of axillary inflammatory and metastatic lymph nodes in rabbit models by using diffusion-weighted imaging: compared with conventional magnetic resonance imaging. Korean J Radiol. 2012; 13:458–466.
Article
21. Eubank WB, Mankoff DA, Takasugi J, Vesselle H, Eary JF, Shanley TJ, et al. 18Fluorodeoxyglucose positron emission tomography to detect mediastinal or internal mammary metastases in breast cancer. J Clin Oncol. 2001; 19:3516–3523.
Article
22. Segaert I, Mottaghy F, Ceyssens S, De Wever W, Stroobants S, Van Ongeval C, et al. Additional value of PET-CT in staging of clinical stage IIB and III breast cancer. Breast J. 2010; 16:617–624.
Article
23. Hindié E, Groheux D, Hennequin C, Zanotti-Fregonara P, Vercellino L, Berenger N, et al. Lymphoscintigraphy can select breast cancer patients for internal mammary chain radiotherapy. Int J Radiat Oncol Biol Phys. 2012; 83:1081–1088.
Article
24. van der Ent FW, Kengen RA, van der Pol HA, Povel JA, Stroeken HJ, Hoofwijk AG. Halsted revisited: internal mammary sentinel lymph node biopsy in breast cancer. Ann Surg. 2001; 234:79–84.
Article
25. Donegan WL. The influence of untreated internal mammary metastases upon the course of mammary cancer. Cancer. 1977; 39:533–538.
Article
26. Huang O, Wang L, Shen K, Lin H, Hu Z, Liu G, et al. Breast cancer subpopulation with high risk of internal mammary lymph nodes metastasis: analysis of 2,269 Chinese breast cancer patients treated with extended radical mastectomy. Breast Cancer Res Treat. 2008; 107:379–387.
Article
27. Lacour J, Bucalossi P, Cacers E, Jacobelli G, Koszarowski T, Le M, et al. Radical mastectomy versus radical mastectomy plus internal mammary dissection: five-year results of an international cooperative study. Cancer. 1976; 37:206–214.
Article
28. Livingston SF, Arlen M. The extended extrapleural radical mastectomy: its role in the treatment of carcinoma of the breast. Ann Surg. 1974; 179:260–265.
29. Coombs NJ, Boyages J, French JR, Ung OA. Internal mammary sentinel nodes: ignore, irradiate or operate? Eur J Cancer. 2009; 45:789–794.
Article
Full Text Links
  • JBC
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr