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Imaging of the Axilla

Variant: 1   Female. New palpable, unilateral, axillary lump. Initial imaging of the axilla.
Procedure Appropriateness Category Relative Radiation Level
US axilla Usually Appropriate O
Digital breast tomosynthesis diagnostic May Be Appropriate ☢☢
Mammography diagnostic May Be Appropriate ☢☢
MRI breast without and with IV contrast Usually Not Appropriate O
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢
FDG-PET/CT skull base to mid-thigh Usually Not Appropriate ☢☢☢☢

Variant: 2   Female. New palpable, bilateral, axillary lump. Initial imaging of the axilla.
Procedure Appropriateness Category Relative Radiation Level
US axilla Usually Appropriate O
Digital breast tomosynthesis diagnostic Usually Not Appropriate ☢☢
Mammography diagnostic Usually Not Appropriate ☢☢
MRI breast without and with IV contrast Usually Not Appropriate O
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢
FDG-PET/CT skull base to mid-thigh Usually Not Appropriate ☢☢☢☢

Variant: 3   Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
Procedure Appropriateness Category Relative Radiation Level
US axilla May Be Appropriate O
MRI breast without and with IV contrast Usually Not Appropriate O
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢
FDG-PET/CT skull base to mid-thigh Usually Not Appropriate ☢☢☢☢

Variant: 4   Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT.
Procedure Appropriateness Category Relative Radiation Level
US axilla Usually Appropriate O
MRI breast without and with IV contrast May Be Appropriate (Disagreement) O
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢
FDG-PET/CT skull base to mid-thigh Usually Not Appropriate ☢☢☢☢

Variant: 5   Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
Procedure Appropriateness Category Relative Radiation Level
US axilla May Be Appropriate O
MRI breast without and with IV contrast May Be Appropriate O
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢
FDG-PET/CT skull base to mid-thigh Usually Not Appropriate ☢☢☢☢

Variant: 6   Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT (prior to treatment).
Procedure Appropriateness Category Relative Radiation Level
US axilla Usually Appropriate O
MRI breast without and with IV contrast May Be Appropriate O
CT chest abdomen pelvis with IV contrast May Be Appropriate ☢☢☢☢
FDG-PET/CT skull base to mid-thigh May Be Appropriate ☢☢☢☢
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢

Variant: 7   Female. Breast cancer, greater than 2 cm in size, at mid-treatment of neoadjuvant chemotherapy, with initial clinical node-negative disease but now presenting with new palpable axillary lump. Imaging of the axilla at mid-treatment.
Procedure Appropriateness Category Relative Radiation Level
US axilla Usually Appropriate O
Digital breast tomosynthesis diagnostic Usually Not Appropriate ☢☢
Mammography diagnostic Usually Not Appropriate ☢☢
MRI breast without and with IV contrast Usually Not Appropriate O
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢
FDG-PET/CT skull base to mid-thigh Usually Not Appropriate ☢☢☢☢

Variant: 8   Female. Breast cancer, greater than 2 cm in size, clinical node-negative. Imaging of the axilla after completion of neoadjuvant chemotherapy.
Procedure Appropriateness Category Relative Radiation Level
US axilla May Be Appropriate (Disagreement) O
MRI breast without and with IV contrast May Be Appropriate O
Digital breast tomosynthesis diagnostic Usually Not Appropriate ☢☢
Mammography diagnostic Usually Not Appropriate ☢☢
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢
FDG-PET/CT skull base to mid-thigh Usually Not Appropriate ☢☢☢☢

Variant: 9   Female. Breast cancer, greater than 2 cm in size, clinical node-positive. Imaging of the axilla after completion of neoadjuvant chemotherapy and prior to surgery.
Procedure Appropriateness Category Relative Radiation Level
US axilla Usually Appropriate O
MRI breast without and with IV contrast May Be Appropriate O
Digital breast tomosynthesis diagnostic Usually Not Appropriate ☢☢
Mammography diagnostic Usually Not Appropriate ☢☢
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢
FDG-PET/CT skull base to mid-thigh Usually Not Appropriate ☢☢☢☢

Variant: 10   Female. Newly diagnosed locally recurrent breast cancer. Initial imaging of the axilla following diagnostic mammography or DBT.
Procedure Appropriateness Category Relative Radiation Level
US axilla May Be Appropriate O
MRI breast without and with IV contrast May Be Appropriate O
FDG-PET/CT skull base to mid-thigh May Be Appropriate ☢☢☢☢
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢

Variant: 11   Female. Suspicious axillary node on mammography or ultrasound. Next imaging study.
Procedure Appropriateness Category Relative Radiation Level
US-guided core biopsy axillary node Usually Appropriate O
US-guided fine needle aspiration biopsy axillary node Usually Appropriate O
MRI breast without and with IV contrast May Be Appropriate (Disagreement) O
MRI breast without IV contrast Usually Not Appropriate O
Sestamibi MBI Usually Not Appropriate ☢☢☢
CT chest abdomen pelvis with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without and with IV contrast Usually Not Appropriate ☢☢☢☢
CT chest abdomen pelvis without IV contrast Usually Not Appropriate ☢☢☢☢
FDG-PET/CT skull base to mid-thigh Usually Not Appropriate ☢☢☢☢

Variant: 12   Female. Suspicious axillary node on any other imaging modality (excluding mammography and ultrasound). Next imaging study.
Procedure Appropriateness Category Relative Radiation Level
US axilla Usually Appropriate O
Digital breast tomosynthesis diagnostic Usually Appropriate ☢☢
Mammography diagnostic Usually Appropriate ☢☢
US-guided core biopsy axillary node May Be Appropriate (Disagreement) O
US-guided fine needle aspiration biopsy axillary node May Be Appropriate O

Panel Members
Summary of Literature Review
Introduction/Background
Special Imaging Considerations
Initial Imaging Definition
Discussion of Procedures by Variant
Variant 1: Female. New palpable, unilateral, axillary lump. Initial imaging of the axilla.
Variant 1: Female. New palpable, unilateral, axillary lump. Initial imaging of the axilla.
A. CT Chest, Abdomen, and Pelvis
Variant 1: Female. New palpable, unilateral, axillary lump. Initial imaging of the axilla.
B. Digital Breast Tomosynthesis Diagnostic
Variant 1: Female. New palpable, unilateral, axillary lump. Initial imaging of the axilla.
C. FDG-PET/CT Skull Base to Mid-Thigh
Variant 1: Female. New palpable, unilateral, axillary lump. Initial imaging of the axilla.
D. Mammography Diagnostic
Variant 1: Female. New palpable, unilateral, axillary lump. Initial imaging of the axilla.
E. MRI Breast
Variant 1: Female. New palpable, unilateral, axillary lump. Initial imaging of the axilla.
F. Sestamibi MBI
Variant 1: Female. New palpable, unilateral, axillary lump. Initial imaging of the axilla.
G. US Axilla
Variant 2: Female. New palpable, bilateral, axillary lump. Initial imaging of the axilla.
Variant 2: Female. New palpable, bilateral, axillary lump. Initial imaging of the axilla.
A. CT Chest, Abdomen, and Pelvis
Variant 2: Female. New palpable, bilateral, axillary lump. Initial imaging of the axilla.
B. Digital Breast Tomosynthesis Diagnostic
Variant 2: Female. New palpable, bilateral, axillary lump. Initial imaging of the axilla.
C. FDG-PET/CT Skull Base to Mid-Thigh
Variant 2: Female. New palpable, bilateral, axillary lump. Initial imaging of the axilla.
D. Mammography Diagnostic
Variant 2: Female. New palpable, bilateral, axillary lump. Initial imaging of the axilla.
E. MRI Breast
Variant 2: Female. New palpable, bilateral, axillary lump. Initial imaging of the axilla.
F. Sestamibi MBI
Variant 2: Female. New palpable, bilateral, axillary lump. Initial imaging of the axilla.
G. US Axilla
Variant 3: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
Variant 3: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
A. CT Chest, Abdomen, and Pelvis
Variant 3: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
B. FDG-PET/CT Skull Base to Mid-Thigh
Variant 3: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
C. MRI Breast
Variant 3: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
D. Sestamibi MBI
Variant 3: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
E. US Axilla
Variant 4: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT.
Variant 4: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT.
A. CT Chest, Abdomen, and Pelvis
Variant 4: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT.
B. FDG-PET/CT Skull Base to Mid-Thigh
Variant 4: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT.
C. MRI Breast
Variant 4: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT.
D. Sestamibi MBI
Variant 4: Female. Newly diagnosed breast cancer, 2 cm or less, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT.
E. US Axilla
Variant 5: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
Variant 5: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
A. CT Chest, Abdomen, and Pelvis
Variant 5: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
B. FDG-PET/CT Skull Base to Mid-Thigh
Variant 5: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
C. MRI Breast
Variant 5: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
D. Sestamibi MBI
Variant 5: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-negative. Initial imaging of the axilla following diagnostic mammography or DBT.
E. US Axilla
Variant 6: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT (prior to treatment).
Variant 6: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT (prior to treatment).
A. CT Chest, Abdomen, and Pelvis
Variant 6: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT (prior to treatment).
B. FDG-PET/CT Skull Base to Mid-Thigh
Variant 6: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT (prior to treatment).
C. MRI Breast
Variant 6: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT (prior to treatment).
D. Sestamibi MBI
Variant 6: Female. Newly diagnosed breast cancer, greater than 2 cm, with clinical node-positive. Initial imaging of the axilla following diagnostic mammography or DBT (prior to treatment).
E. US Axilla
Variant 7: Female. Breast cancer, greater than 2 cm in size, at mid-treatment of neoadjuvant chemotherapy, with initial clinical node-negative disease but now presenting with new palpable axillary lump. Imaging of the axilla at mid-treatment.
Variant 7: Female. Breast cancer, greater than 2 cm in size, at mid-treatment of neoadjuvant chemotherapy, with initial clinical node-negative disease but now presenting with new palpable axillary lump. Imaging of the axilla at mid-treatment.
A. CT Chest, Abdomen, and Pelvis
Variant 7: Female. Breast cancer, greater than 2 cm in size, at mid-treatment of neoadjuvant chemotherapy, with initial clinical node-negative disease but now presenting with new palpable axillary lump. Imaging of the axilla at mid-treatment.
B. Digital Breast Tomosynthesis Diagnostic
Variant 7: Female. Breast cancer, greater than 2 cm in size, at mid-treatment of neoadjuvant chemotherapy, with initial clinical node-negative disease but now presenting with new palpable axillary lump. Imaging of the axilla at mid-treatment.
C. FDG-PET/CT Skull Base to Mid-Thigh
Variant 7: Female. Breast cancer, greater than 2 cm in size, at mid-treatment of neoadjuvant chemotherapy, with initial clinical node-negative disease but now presenting with new palpable axillary lump. Imaging of the axilla at mid-treatment.
D. Mammography Diagnostic
Variant 7: Female. Breast cancer, greater than 2 cm in size, at mid-treatment of neoadjuvant chemotherapy, with initial clinical node-negative disease but now presenting with new palpable axillary lump. Imaging of the axilla at mid-treatment.
E. MRI Breast
Variant 7: Female. Breast cancer, greater than 2 cm in size, at mid-treatment of neoadjuvant chemotherapy, with initial clinical node-negative disease but now presenting with new palpable axillary lump. Imaging of the axilla at mid-treatment.
F. Sestamibi MBI
Variant 7: Female. Breast cancer, greater than 2 cm in size, at mid-treatment of neoadjuvant chemotherapy, with initial clinical node-negative disease but now presenting with new palpable axillary lump. Imaging of the axilla at mid-treatment.
G. US Axilla
Variant 8: Female. Breast cancer, greater than 2 cm in size, clinical node-negative. Imaging of the axilla after completion of neoadjuvant chemotherapy.
Variant 8: Female. Breast cancer, greater than 2 cm in size, clinical node-negative. Imaging of the axilla after completion of neoadjuvant chemotherapy.
A. CT Chest, Abdomen, and Pelvis
Variant 8: Female. Breast cancer, greater than 2 cm in size, clinical node-negative. Imaging of the axilla after completion of neoadjuvant chemotherapy.
B. Digital Breast Tomosynthesis Diagnostic
Variant 8: Female. Breast cancer, greater than 2 cm in size, clinical node-negative. Imaging of the axilla after completion of neoadjuvant chemotherapy.
C. FDG-PET/CT Skull Base to Mid-Thigh
Variant 8: Female. Breast cancer, greater than 2 cm in size, clinical node-negative. Imaging of the axilla after completion of neoadjuvant chemotherapy.
D. Mammography Diagnostic
Variant 8: Female. Breast cancer, greater than 2 cm in size, clinical node-negative. Imaging of the axilla after completion of neoadjuvant chemotherapy.
E. MRI Breast
Variant 8: Female. Breast cancer, greater than 2 cm in size, clinical node-negative. Imaging of the axilla after completion of neoadjuvant chemotherapy.
F. Sestamibi MBI
Variant 8: Female. Breast cancer, greater than 2 cm in size, clinical node-negative. Imaging of the axilla after completion of neoadjuvant chemotherapy.
G. US Axilla
Variant 9: Female. Breast cancer, greater than 2 cm in size, clinical node-positive. Imaging of the axilla after completion of neoadjuvant chemotherapy and prior to surgery.
Variant 9: Female. Breast cancer, greater than 2 cm in size, clinical node-positive. Imaging of the axilla after completion of neoadjuvant chemotherapy and prior to surgery.
A. CT Chest, Abdomen, and Pelvis
Variant 9: Female. Breast cancer, greater than 2 cm in size, clinical node-positive. Imaging of the axilla after completion of neoadjuvant chemotherapy and prior to surgery.
B. Digital Breast Tomosynthesis Diagnostic
Variant 9: Female. Breast cancer, greater than 2 cm in size, clinical node-positive. Imaging of the axilla after completion of neoadjuvant chemotherapy and prior to surgery.
C. FDG-PET/CT Skull Base to Mid-Thigh
Variant 9: Female. Breast cancer, greater than 2 cm in size, clinical node-positive. Imaging of the axilla after completion of neoadjuvant chemotherapy and prior to surgery.
D. Mammography Diagnostic
Variant 9: Female. Breast cancer, greater than 2 cm in size, clinical node-positive. Imaging of the axilla after completion of neoadjuvant chemotherapy and prior to surgery.
E. MRI Breast
Variant 9: Female. Breast cancer, greater than 2 cm in size, clinical node-positive. Imaging of the axilla after completion of neoadjuvant chemotherapy and prior to surgery.
F. Sestamibi MBI
Variant 9: Female. Breast cancer, greater than 2 cm in size, clinical node-positive. Imaging of the axilla after completion of neoadjuvant chemotherapy and prior to surgery.
G. US Axilla
Variant 10: Female. Newly diagnosed locally recurrent breast cancer. Initial imaging of the axilla following diagnostic mammography or DBT.
Variant 10: Female. Newly diagnosed locally recurrent breast cancer. Initial imaging of the axilla following diagnostic mammography or DBT.
A. CT Chest, Abdomen, and Pelvis
Variant 10: Female. Newly diagnosed locally recurrent breast cancer. Initial imaging of the axilla following diagnostic mammography or DBT.
B. FDG-PET/CT Skull Base to Mid-Thigh
Variant 10: Female. Newly diagnosed locally recurrent breast cancer. Initial imaging of the axilla following diagnostic mammography or DBT.
C. MRI Breast
Variant 10: Female. Newly diagnosed locally recurrent breast cancer. Initial imaging of the axilla following diagnostic mammography or DBT.
D. Sestamibi MBI
Variant 10: Female. Newly diagnosed locally recurrent breast cancer. Initial imaging of the axilla following diagnostic mammography or DBT.
E. US Axilla
Variant 11: Female. Suspicious axillary node on mammography or ultrasound. Next imaging study.
Variant 11: Female. Suspicious axillary node on mammography or ultrasound. Next imaging study.
A. CT Chest, Abdomen, and Pelvis
Variant 11: Female. Suspicious axillary node on mammography or ultrasound. Next imaging study.
B. FDG-PET/CT Skull Base to Mid-Thigh
Variant 11: Female. Suspicious axillary node on mammography or ultrasound. Next imaging study.
C. MRI Breast
Variant 11: Female. Suspicious axillary node on mammography or ultrasound. Next imaging study.
D. Sestamibi MBI
Variant 11: Female. Suspicious axillary node on mammography or ultrasound. Next imaging study.
E. US-Guided Core Biopsy Axillary Node
Variant 11: Female. Suspicious axillary node on mammography or ultrasound. Next imaging study.
F. US-Guided Fine Needle Aspiration Biopsy Axillary Node
Variant 12: Female. Suspicious axillary node on any other imaging modality (excluding mammography and ultrasound). Next imaging study.
Variant 12: Female. Suspicious axillary node on any other imaging modality (excluding mammography and ultrasound). Next imaging study.
A. Digital Breast Tomosynthesis Diagnostic
Variant 12: Female. Suspicious axillary node on any other imaging modality (excluding mammography and ultrasound). Next imaging study.
B. Mammography Diagnostic
Variant 12: Female. Suspicious axillary node on any other imaging modality (excluding mammography and ultrasound). Next imaging study.
C. US Axilla
Variant 12: Female. Suspicious axillary node on any other imaging modality (excluding mammography and ultrasound). Next imaging study.
D. US-Guided Core Biopsy Axillary Node
Variant 12: Female. Suspicious axillary node on any other imaging modality (excluding mammography and ultrasound). Next imaging study.
E. US-Guided Fine Needle Aspiration Biopsy Axillary Node
Summary of Recommendations
Supporting Documents

The evidence table, literature search, and appendix for this topic are available at https://acsearch.acr.org/list. The appendix includes the strength of evidence assessment and the final rating round tabulations for each recommendation.

For additional information on the Appropriateness Criteria methodology and other supporting documents, please go to the ACR website at https://www.acr.org/Clinical-Resources/Clinical-Tools-and-Reference/Appropriateness-Criteria.

Appropriateness Category Names and Definitions

Appropriateness Category Name

Appropriateness Rating

Appropriateness Category Definition

Usually Appropriate

7, 8, or 9

The imaging procedure or treatment is indicated in the specified clinical scenarios at a favorable risk-benefit ratio for patients.

May Be Appropriate

4, 5, or 6

The imaging procedure or treatment may be indicated in the specified clinical scenarios as an alternative to imaging procedures or treatments with a more favorable risk-benefit ratio, or the risk-benefit ratio for patients is equivocal.

May Be Appropriate (Disagreement)

5

The individual ratings are too dispersed from the panel median. The different label provides transparency regarding the panel’s recommendation. “May be appropriate” is the rating category and a rating of 5 is assigned.

Usually Not Appropriate

1, 2, or 3

The imaging procedure or treatment is unlikely to be indicated in the specified clinical scenarios, or the risk-benefit ratio for patients is likely to be unfavorable.

Relative Radiation Level Information
References
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Disclaimer
The ACR Committee on Appropriateness Criteria and its expert panels have developed criteria for determining appropriate imaging examinations for diagnosis and treatment of specified medical condition(s). These criteria are intended to guide radiologists, radiation oncologists and referring physicians in making decisions regarding radiologic imaging and treatment. Generally, the complexity and severity of a patient’s clinical condition should dictate the selection of appropriate imaging procedures or treatments. Only those examinations generally used for evaluation of the patient’s condition are ranked.  Other imaging studies necessary to evaluate other co-existent diseases or other medical consequences of this condition are not considered in this document.  The availability of equipment or personnel may influence the selection of appropriate imaging procedures or treatments. Imaging techniques classified as investigational by the FDA have not been considered in developing these criteria; however, study of new equipment and applications should be encouraged.  The ultimate decision regarding the appropriateness of any specific radiologic examination or treatment must be made by the referring physician and radiologist in light of all the circumstances presented in an individual examination