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JW - 1 - BR (1) Ed Final
JW - 1 - BR (1) Ed Final
Article
European guidelines for the diagnosis, treatment and follow-up of breast lesions
with uncertain malignant potential (B3 lesions) developed jointly by EUSOMA,
EUSOBI, ESP (BWG) and ESSO Isabel T. Rubio a,c,v,*, Lynda Wyld b,w,
Lorenza Marotti c, Alexandra Athanasiou d, Peter Regitnig e, Giuseppe
Catanuto f,g, Jan W. Schoones h, Marzia Zambon i, Julia Camps j, Donatella
Santini k, Jill Dietz l, Francesco Sardanelli m,n, Zsuzsanna Varga o, Marjolein
Smidt p,q, Nisha Sharma r, Abeer M. Shaaban s,t, Fiona Gilbert u,
Introduction
B3 is a group of non-malignant breast lesions with a heterogeneous risk of concurrent or
subsequent breast cancer diagnosis over time. Traditionally, B3 lesions have been treated with
diagnostic surgical open excision because of the risk of upgrade to malignant lesions. But
surgical excision should be reserved for discordant lesions, large lesions that are under-
sampled, and for ADH in many cases. However, many of them were downgraded to benign
lesions at final histology. Discordant report of breast core needle biopsy [CNB] or a B3 report
on biopsy is a challenge and invites further specialized evaluation and varied strategies of
management. The underlying reasons for special consideration in B3 lesions is possibility of
missed malignancy, a high risk lesion progressing to malignancy or a pure harmless benign
lesion. Contemporary management based on facilities available and patient involvement in
decision making, together range from expectant conservatism to upfront surgery, prevention
strategies and lifestyle changes.
Clustered
Monotonous calcification
intradutal epithelial
lesions Special imaging
<2mm focus may aid[MRI/CE]
If VAB/VAR Concordance:
2. ALH, LCIS[Atypical lobular Surveillance, not surgery
Hyerplasia, Lobular Carcinoma Evidence/Grade11/B
In Imaging discordance: Surgical
in Situ]
Excision/ VAE
No B/L Mastectomy in the absence of
high risk factors 111/B
Patient information and shared decision
making
Discohesive, Non mass
Multifocal/Bilateral enhancement :MRI
LCIS Type A LCIS Type B
type A/ Type B occult/calcification
:small/ large nucleus outside lesion
cells
3. FEA[Flat epithelial Atypia] In case of concordant imaging:
Surveillance 11/B
Columnar Cell
Concomitant with ADH on CNB:
Lesiona[CCL]
Surgical excision/VAE 11/B
Concomitant with ADH on VAB:
Residual calcification or discordant
imaging: Surgical excision/ VAE
111/B
Columnar cell Groupeg
Change{CCC]/Hyperpla amorphous
sia[CCH] calcifications
Stellate
Central fibroelastic
lesion/architectural
core that lacks
distorsion,
Stellate orientation, Radiolucent centre,
fibroelastic stroma no enhancement on
MRI
Fibrovascular
core, size<3mm
Open excision to know the real nature
6. Apocrine Adenosis of lesion. Upgrade rate is 16.7-25%
Resembles Low
Grade DCIS
Features of
malignancy to
Mucus pools without be ruled out
epithelial cells
Differentiation difficult
Concluding remarks
1. VAB can upgrade the reports received on CNB
2. Treatment based on VAB report is likely to decrease surgical interventions
3. Discordant biopsy and imaging favor surgical excision
4. Large Fibroepithelial lesions may be excised in view of suspicion of phyllodes tumour
and chances of recurrence
5. In view of lack of facilities of VAB, patient factors especially compliance with respect
to follow up, especially in low resource set ups,surgical excision is a viable option
with ongoing efforts to upgrade technology to be able to safely reduce surgical
excisions
6. Preventive strategies incorporated in clinical practice are a useful tool to decrease
cancer burden