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Paper |

Sonographic Hematoma-Guided vs Wire-Localized Lumpectomy for Breast Cancer:  A Comparison of Margins and Volume of Resection FREE

Rakhshanda Layeequr Rahman, MD; Elaine Iuanow, MD; Sybil Crawford, MS; Robert Quinlan, MD
[+] Author Affiliations

Departments of Surgery (Drs Layeequr Rahman and Quinlan), Radiology (Dr Iuanow), and Behavioral Sciences (Ms Crawford), UMass Memorial Health Care, Worcester, Mass.


Arch Surg. 2007;142(4):343-346. doi:10.1001/archsurg.142.4.343.
Text Size: A A A
Published online

Hypothesis  Sonographic hematoma-guided (SHG) lumpectomy achieves better margin clearance with a smaller volume of resection compared with wire-localized (WL) lumpectomy.

Design  Retrospective study.

Setting  University Comprehensive Breast Center.

Patients  Consecutive patients treated over 6 months at the breast center with stereotactic biopsy–proven cancers that were not visualized on ultrasonography. The SHG and WL techniques were compared.

Main Outcome Measures  The matching variables were age, mammographic abnormality, tumor size and type, and lymph node status. The outcome variables were the closest margin of resection, volume of resection, resection index (resection volume divided by tumor volume), and rate of margin revision.

Results  Twenty-nine patients had SHG lumpectomy and 34 had WL lumpectomy. The SHG and WL groups were similar in age, mammographic abnormality, tumor size and type, and lymph node status. The median (interquartile range) closest margin was 5.0 (5-8) mm in the SHG group vs 3.5 (1-7) mm in the WL group ( = .01). The median (interquartile range) resection volume was 85.0 (60-128) cm3 in the SHG group vs 143.4 (54-229) cm3 in the WL group ( = .048). The median (interquartile range) resection index was 77.1 (51-220) in the SHG group vs 315.9 (89-3025) in the WL group ( = .003). The margin was revised in 1 (3.4%) of the patients who underwent SHG lumpectomy vs 5 (14.7%) of the patients who underwent WL lumpectomy ( = .20).

Conclusions  Sonographic hematoma-guided lumpectomy is superior to WL lumpectomy in obtaining adequate margins while minimizing the volume of resection.

Screening mammography and advanced imaging techniques have increased the rate of detection of nonpalpable cancers in the breast that are amenable to conservation therapy. The goal of breast conservation in the treatment of cancer is to achieve an oncologic resection with adequate margins while maintaining cosmesis. This poses significant challenges in the case of nonpalpable lesions and requires image-guided localization to effect resection. The current standard technique of operative guidance is preoperative wire localization (WL), which is associated with several limitations. First, the ideal entry site for the radiologist is often distant from the ideal incision site for the surgeon. Second, surgeons depend on 2-dimensional postlocalization radiographs to estimate the 3-dimensional position of the lesion in relation to the wire, which results in positive margins in up to 62% of patients.13 Third, up to 10% of patients have vasovagal episodes during wire placement.4,5 Fourth, complications such as wire transection6 and displacement have been described.7,8 Last but not least are the logistic issues that arise between surgical and radiological scheduling systems.

These disadvantages have led to the quest for better alternatives to WL. Intraoperative ultrasonography has proven to be superior to WL in all of the aforementioned aspects for lesions that are visible on ultrasonography.912 Unfortunately, 60% to 70% of mammographic lesions are not visible on ultrasonography and the onus of acceptable oncoplastic resection continues to fall on WL.

Smith et al13 described the use of the sonographically visible hematoma (induced iatrogenically by stereotactic biopsy) as a localizing device with intraoperative ultrasonography. Postbiopsy hematoma is a naturally occurring localizing device that is visible on ultrasonography without the need for another invasive procedure. We hypothesized that sonographic hematoma-guided (SHG) lumpectomy for breast cancer effects better resection margins by providing all dimensions of the lesion and results in better cosmetic outcome by ensuring a lower volume of resection.

PATIENTS

Sixty-three consecutive patients treated with breast conservation at the Comprehensive Breast Center between October 1, 2005, and March 31, 2006, for stereotactic biopsy–proven small unifocal cancers that were not visualized on ultrasonography were studied. Patients with extensive lesions requiring bracketing wires were excluded. UMass Memorial Health Center, Worcester, Mass, is a university-based practice that has a multispecialty-based Comprehensive Breast Center with 3 breast surgeons. Two surgeons (R.M.Q. and Anne Larkin, MD) use WL for lumpectomies and 1 surgeon (R.L.R.) performs SHG resection for breast cancer. The rest of the management protocols are similar across the entire practice.

SHG EXCISION TECHNIQUE

This technique involves using the iatrogenic hematoma as a localization device that is created during stereotactic biopsy of the mammographic lesion. Patients are evaluated in the office within 7 to 10 days of biopsy, where the sonographic visibility of the hematoma is documented by the surgeon with a focused ultrasonographic scan of the breast using triangulation based on the mammographic results. Surgery is performed ideally within 4 to 5 weeks of biopsy, lest the hematoma resolves. An intraoperative ultrasonographic scan of the documented area is performed by the surgeon, and skin markings are made at the site of hematoma as well as at a 1-cm margin from the edge to affect ultrasonography-guided excision. Specimen ultrasonography is performed to document the presence of the hematoma with adequate margins. Suspected close margins can be revised as additional shaved margins during the same surgery. The specimen is oriented and submitted for pathological analysis.

DATA COLLECTION

Data were collected from the medical records regarding patient age, mammographic abnormality, tumor size and type, and lymph node status for matching between the 2 groups. The closest margin, the volume of resection, the need for reexcision, and the cosmetic outcome score by the patient using a visual analog scale of 0 to 10 were recorded as outcome variables.

STATISTICAL ANALYSIS

Microsoft Excel software (Microsoft Corp, Redmond, Wash) was used to record the data. The differences in age, mammographic abnormality, tumor type, and tumor size were computed for matching between the WL and SHG groups. The tumor volume and the volume of resection were calculated from the 3 dimensions of the tumor and the specimen described in all of the reports of the pathological analysis; the resection index was computed as a ratio of resection volume and tumor volume such that the lower the index is, the better the cosmetic resection is. SigmaStat software version 2.0 (SPSS, Inc, Chicago, Ill) was used for statistical significance.

Sixty-three patients were treated for stereotactically diagnosed nonpalpable breast cancer that was not visible on ultrasonography during the study period. Thirty-four patients (54.0%) underwent WL lumpectomy and 29 (46.0%) were subjected to SHG resection. The 2 groups were similar in age, mammographic abnormality, and tumor characteristics (Table 1). The tumor volume was larger in the SHG group with borderline statistical significance ( = .07). The comparison of outcome variables between the 2 groups is depicted in Table 2. The median (interquartile range) closest margin was 5.0 (5-8) mm in the SHG group vs 3.5 (1-7) mm in the WL group ( = .01). The volume of resection was significantly larger in the WL group (median, 143.4 cm3) despite the smaller volume of the tumor. The median (interquartile range) resection index was 77.1 (51-220) in the SHG group vs 315.9 (89-3025) in the WL group ( = .003). The median (interquartile range) cosmetic outcome score was 6 (5-8) for the patients in WL group vs 9 (7-9) for the patients in the SHG group ( = .03). Only 1 patient (3.4%) needed margin revision in the SHG group as compared with 5 patients (14.7%) in the WL group who needed margin revision; however, this difference was not statistically significant ( = .20).

Table Graphic Jump LocationTable 1. Comparison of Baseline Characteristics Between Wire-Localized and Sonographic Hematoma-Guided Lumpectomy Groups
Table Graphic Jump LocationTable 2. Comparison of Main Outcome Measures Between Wire-Localized and Sonographic Hematoma-Guided Lumpectomy Groups

The ideal localization procedure for nonpalpable breast cancers would provide precise identification of the site of the lesion with adequate intraoperative assessment of margins such that the rate of reexcision is limited and the cosmetic outcome is acceptable. In addition, it would be painless and convenient for patients and would not hamper the surgical scheduling. The current standard of WL falls short on these criteria19; hence, the pursuit to develop alternative methods continues. The SHG technique is an immense improvement over WL to meet the mentioned criteria.

First, the hematoma is a natural result of biopsy, thereby completely obviating the need for another localization procedure. This eliminates the patient's inconvenience associated with an invasive procedure without anesthesia, pain, and vasovagal episodes. Second, the position of the hematoma within the breast is always at the site of the lesion compared with the wire, which is placed at an approximated close location. This issue is further complicated in situations where the original lesion is completely excised during the biopsy and the wire is placed using the clip as a guide. Clip migration occurs in about half of the cases,14,15 adding to the challenge of localization. These factors are probably responsible for the high rate of positive margins after WL lumpectomy. Our data show the positive margin rate in the WL group to be 15%, which is much lower than that reported in the literature.16 In this group, clip migration occurred in only 3 patients and was not associated with positive margins. Although in this study both techniques had comparable margin clearance, the volume of resection was significantly larger in the WL group, which in turn may have contributed to the lower cosmetic outcome score. It is established that cosmetic outcome worsens as the resection volume increases.17 Taylor et al18 found that the resection volume of 100 cm3 is associated with cosmetic compromise irrespective of breast size. Our data show that SHG lumpectomy achieved good margins with a much smaller volume of resection compared with WL (median resection volume, 85.0 cm3 vs 143.4 cm3, respectively). Third, sonographic assessment in the operating room provides appropriate assessment of all margins to plan excision, and specimen ultrasonography can guide immediately if a margin revision is indicated.13 In our study, 2 margins were revised intraoperatively based on specimen ultrasonography. Finally, from a logistic standpoint, SHG excision obviates the need for radiology scheduling; moreover, specimen ultrasonography is much faster than specimen radiography, thereby enhancing efficiency in the operating room. Admittedly, the SHG technique is not without problems. There is a learning curve involved in the use of ultrasonography technology by the surgeons. In addition, localization is not possible if the diagnosis is established by fine-needle aspiration and may be compromised if the biopsy is associated with significant hemorrhage causing a large hematoma or if multiple needle insertions are performed. However, it is becoming increasingly clear that ultrasonography has become an indispensable tool for the breast surgeon in the office and the operating room setting. Several studies have shown the accuracy and convenience of surgeon-based breast ultrasonography19; our study demonstrates the effect of surgeon-performed intraoperative ultrasonography on the quality of breast cancer treatment in terms of adequate excision, patient friendliness, and cosmetic superiority with an added value of obviating the logistics of scheduling.

Other techniques for nonpalpable lesions involve radioisotope-guided excision with technetium Tc 99m–labeled colloid injection20,21 or radioactive seed placement.22 Although both of these approaches achieve better margins and superior cosmetic outcome, they have certain shortcomings. First, an extra procedure is required for localization after the diagnosis of cancer or a high-risk lesion is established. Scheduling issues between 2 departments are curtailed but still exist. Shine-through radioactivity can potentially compromise the sentinel node procedure in the case of technetium Tc 99m use, and the Compton effect has to be considered with the use of radioactivity. Last but not least, exposure to radioactivity is eventually going to limit the use of the procedure. With the current Occupational Safety and Health Administration guidelines23 and radioactivity exposure to the surgeons by the sentinel node biopsy procedure,24 surgeons can perform about 100 procedures per year; adding another procedure with radioactivity exposure is likely to limit the number of procedures each surgeon can perform per year without exceeding the recommended dose.

In conclusion, we believe that SHG resection for nonpalpable breast cancer is a simple, convenient (for patients and surgeons), and accurate technique for localization that ensures adequate margins while keeping the resection volume to a minimum.

Rakhshanda Layeequr Rahman, MD, Department of Surgery, UMass Memorial Health Care, 119 Belmont St, Worcester, MA 01605 (layeequr@ummhc.org).

November 1, 2006.

: Layeequr Rahman and Quinlan. : Layeequr Rahman and Iuanow. : Layeequr Rahman and Crawford. : Layeequr Rahman. : Layeequr Rahman, Iuanow, Crawford, and Quinlan. : Crawford. : Layeequr Rahman and Iuanow. : Quinlan.

None reported.

This paper was presented at the 87th Annual Meeting of the New England Surgical Society; September 16, 2006; Groton, Conn; and is published after peer review and revision. The discussions that follow this article are based on the originally submitted manuscript and not the revised manuscript.

Would there be any advantage to doing an ultrasound-guided needle localization so that you have something solid in there when you are cutting down vs just making some lines on the skin, which may move around afterwards?

I think it is a learning curve and comfort zone issue. Many surgeons would put a wire in to be able to feel something within the breast, but I think the wire is a thin structure so localization is good, but margins, still I would rely on staying 1 cm based on my image because the wire will not give me an idea about that.

Do you use any oncoplastic techniques, because the difference in volume resected may not be important if you know how to put things back together again. Ultrasound in the OR [operating room] may be out of the reach of many surgeons.

When we have to, if the volume of resection has to be high, we do employ oncoplastic techniques, but I think the idea would be you do not want to resect the tissue if you do not have to for a margin's sake but yes, of course, if you are bound to from an oncologic standpoint, then you would employ techniques to do that.

I enjoyed the paper. I wonder, is it the same surgeon doing a wire localization as is doing the hematoma localization?

No.

That might influence the results, do you think?

Yes. That is why I looked at some matching variables, but yes, that bias we cannot remove.

Dr Quinlan was doing the wire ones, wasn't he?

Yes.

None reported.

Acosta  JAGreenlee  JA Surgical margins after needle localization breast biopsy. Am J Surg 1995;170643- 645
PubMed Link to Article
Kaufman  CSDelbecq  RJacobson  L Excising the reexcision: stereotactic core biopsy decreases the need for reexcision of breast cancer. World J Surg 1998;221023- 1028
PubMed Link to Article
Cangiarella  JGroos  JSymmans  WF  et al.  The incidence of positive margins with breast conserving therapy following mammotome biopsy for microcalcification. J Surg Oncol 2000;74263- 266
PubMed Link to Article
Rissanen  TJMakarainen  HPMattila  SI  et al.  Wire localized biopsy of breast lesions: a review of 425 cases found in screening or clinical mammography. Clin Radiol 1993;4714- 22
PubMed Link to Article
Helvie  MAIkeda  DMAdler  DD Localization and needle aspiration of breast lesions: complications in 370 cases. AJR Am J Roentgenol 1991;157711- 714
PubMed Link to Article
Homer  MJ Transection of the localization hooked wire during breast biopsy. AJR Am J Roentgenol 1983;141929- 930
PubMed Link to Article
Bristol  JBJones  PA Transgression of localizing wire into the pleural cavity prior to mammography. Br J Radiol 1981;54139- 140
PubMed Link to Article
Davis  PSWexhsler  RJFeig  SA  et al.  Migration of breast biopsy localization wire. AJR Am J Roentgenol 1988;150787- 788
PubMed Link to Article
Snider  HC  JrMorrison  DG Intraoperative ultrasound localization of nonpalpable breast lesions. Ann Surg Oncol 1999;6308- 314
PubMed Link to Article
Rahusen  FDTaets van Amerongen  AHvan Diest  PJBorgstein  PJBleichrodt  RPMeijer  S Ultrasound-guided lumpectomy of nonpalpable breast cancer: a feasibility study looking at the accuracy of obtained margins. J Surg Oncol 1999;7272- 76
PubMed Link to Article
Harlow  SPKrag  DNAmes  SEWeaver  DL Intraoperative ultrasound localization to guide surgical excision of nonpalpable breast carcinoma. J Am Coll Surg 1999;189241- 246
PubMed Link to Article
Rahusen  FDBremers  AJFabry  HFvan Amerongen  AHBoom  RPMeijer  S Ultrasound-guided lumpectomy of nonpalpable breast cancer vs wire-guided resection: a randomized clinical trial. Ann Surg Oncol 2002;9994- 998
PubMed Link to Article
Smith  LFHenry-Tillman  RRubio  ITKorourian  SKlimberg  VS Intraoperative localization after stereotactic biopsy without a needle. Am J Surg 2001;182584- 589
PubMed Link to Article
Kass  RKlimberg  VSKass  L  et al.  Clip migration in stereotactic biopsy. Am J Surg 2002;184325- 331
PubMed Link to Article
Esserman  LECura  MADaCosta  D Recognizing pitfalls in early and late migration of clip markers after image-guided directional vacuum-assisted biopsy. Radiographics 2004;24147- 156
PubMed Link to Article
Nurko  JMancino  ATWhitacre  EEdwards  MJ Surgical benefits conveyed by biopsy site marking system using ultrasound localization. Am J Surg 2005;190618- 622
PubMed Link to Article
Audisio  RANadeem  RThind  RHarris  ODesmond  SChagla  LS Radioguided occult lesion localization (ROLL) for non-palpable breast lesions: the localization method of choice is now available in UK. Ann R Coll Surg Engl 2005;8792- 95
PubMed Link to Article
Taylor  MEPerez  CAHalverson  KJ  et al.  Factors influencing cosmetic results after conservation therapy for breast cancer. Int J Radiat Oncol Biol Phys 1995;31753- 764
PubMed Link to Article
Fine  REStaren  ED Updates in breast ultrasound. Surg Clin North Am 2004;841001- 1034
PubMed Link to Article
Paganelli  GVeronesi  U Innovation in early breast cancer surgery: radio-guided occult lesion localization and sentinel node biopsy. Nucl Med Commun 2002;23625- 627
PubMed Link to Article
Paganelli  GLuini  AVeronesi  U Radioguided occult lesion localization (ROLL) in breast cancer: maximizing efficacy, minimizing mutilation. Ann Oncol 2002;131839- 1840
PubMed Link to Article
Gray  RJPockaj  BAKarstaedt  PJRoarke  MC Radioactive seed localization of nonpalpable breast lesions is better than wire localization. Am J Surg 2004;188377- 380
PubMed Link to Article
Occupational Safety and Health Administration, Ionizing radiation.  Washington, DC Occupational Safety & Health Administration1998;1- 9
De Kanter  AYArends  PPEggermont  AMM  et al.  Radiation protection for the sentinel node procedure in breast cancer. Eur J Surg Oncol 2003;29396- 399
PubMed Link to Article

Figures

Tables

Table Graphic Jump LocationTable 1. Comparison of Baseline Characteristics Between Wire-Localized and Sonographic Hematoma-Guided Lumpectomy Groups
Table Graphic Jump LocationTable 2. Comparison of Main Outcome Measures Between Wire-Localized and Sonographic Hematoma-Guided Lumpectomy Groups

References

Acosta  JAGreenlee  JA Surgical margins after needle localization breast biopsy. Am J Surg 1995;170643- 645
PubMed Link to Article
Kaufman  CSDelbecq  RJacobson  L Excising the reexcision: stereotactic core biopsy decreases the need for reexcision of breast cancer. World J Surg 1998;221023- 1028
PubMed Link to Article
Cangiarella  JGroos  JSymmans  WF  et al.  The incidence of positive margins with breast conserving therapy following mammotome biopsy for microcalcification. J Surg Oncol 2000;74263- 266
PubMed Link to Article
Rissanen  TJMakarainen  HPMattila  SI  et al.  Wire localized biopsy of breast lesions: a review of 425 cases found in screening or clinical mammography. Clin Radiol 1993;4714- 22
PubMed Link to Article
Helvie  MAIkeda  DMAdler  DD Localization and needle aspiration of breast lesions: complications in 370 cases. AJR Am J Roentgenol 1991;157711- 714
PubMed Link to Article
Homer  MJ Transection of the localization hooked wire during breast biopsy. AJR Am J Roentgenol 1983;141929- 930
PubMed Link to Article
Bristol  JBJones  PA Transgression of localizing wire into the pleural cavity prior to mammography. Br J Radiol 1981;54139- 140
PubMed Link to Article
Davis  PSWexhsler  RJFeig  SA  et al.  Migration of breast biopsy localization wire. AJR Am J Roentgenol 1988;150787- 788
PubMed Link to Article
Snider  HC  JrMorrison  DG Intraoperative ultrasound localization of nonpalpable breast lesions. Ann Surg Oncol 1999;6308- 314
PubMed Link to Article
Rahusen  FDTaets van Amerongen  AHvan Diest  PJBorgstein  PJBleichrodt  RPMeijer  S Ultrasound-guided lumpectomy of nonpalpable breast cancer: a feasibility study looking at the accuracy of obtained margins. J Surg Oncol 1999;7272- 76
PubMed Link to Article
Harlow  SPKrag  DNAmes  SEWeaver  DL Intraoperative ultrasound localization to guide surgical excision of nonpalpable breast carcinoma. J Am Coll Surg 1999;189241- 246
PubMed Link to Article
Rahusen  FDBremers  AJFabry  HFvan Amerongen  AHBoom  RPMeijer  S Ultrasound-guided lumpectomy of nonpalpable breast cancer vs wire-guided resection: a randomized clinical trial. Ann Surg Oncol 2002;9994- 998
PubMed Link to Article
Smith  LFHenry-Tillman  RRubio  ITKorourian  SKlimberg  VS Intraoperative localization after stereotactic biopsy without a needle. Am J Surg 2001;182584- 589
PubMed Link to Article
Kass  RKlimberg  VSKass  L  et al.  Clip migration in stereotactic biopsy. Am J Surg 2002;184325- 331
PubMed Link to Article
Esserman  LECura  MADaCosta  D Recognizing pitfalls in early and late migration of clip markers after image-guided directional vacuum-assisted biopsy. Radiographics 2004;24147- 156
PubMed Link to Article
Nurko  JMancino  ATWhitacre  EEdwards  MJ Surgical benefits conveyed by biopsy site marking system using ultrasound localization. Am J Surg 2005;190618- 622
PubMed Link to Article
Audisio  RANadeem  RThind  RHarris  ODesmond  SChagla  LS Radioguided occult lesion localization (ROLL) for non-palpable breast lesions: the localization method of choice is now available in UK. Ann R Coll Surg Engl 2005;8792- 95
PubMed Link to Article
Taylor  MEPerez  CAHalverson  KJ  et al.  Factors influencing cosmetic results after conservation therapy for breast cancer. Int J Radiat Oncol Biol Phys 1995;31753- 764
PubMed Link to Article
Fine  REStaren  ED Updates in breast ultrasound. Surg Clin North Am 2004;841001- 1034
PubMed Link to Article
Paganelli  GVeronesi  U Innovation in early breast cancer surgery: radio-guided occult lesion localization and sentinel node biopsy. Nucl Med Commun 2002;23625- 627
PubMed Link to Article
Paganelli  GLuini  AVeronesi  U Radioguided occult lesion localization (ROLL) in breast cancer: maximizing efficacy, minimizing mutilation. Ann Oncol 2002;131839- 1840
PubMed Link to Article
Gray  RJPockaj  BAKarstaedt  PJRoarke  MC Radioactive seed localization of nonpalpable breast lesions is better than wire localization. Am J Surg 2004;188377- 380
PubMed Link to Article
Occupational Safety and Health Administration, Ionizing radiation.  Washington, DC Occupational Safety & Health Administration1998;1- 9
De Kanter  AYArends  PPEggermont  AMM  et al.  Radiation protection for the sentinel node procedure in breast cancer. Eur J Surg Oncol 2003;29396- 399
PubMed Link to Article

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