• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of jclinpathJournal of Clinical PathologyVisit this articleSubmit a manuscriptReceive email alertsContact usBMJ
J Clin Pathol. Dec 2007; 60(12): 1321–1327.
Published online Dec 20, 2006. doi:  10.1136/jcp.2006.040642
PMCID: PMC2095562

Non‐operative breast pathology: lobular neoplasia

Abstract

Lobular neoplasia is a relatively uncommon lesion, which is frequently diagnosed in biopsy specimens taken for other reasons. Although the histological features of this lesion are well known, its biological significance as a “risk indicator” or “breast cancer precursor” has been a matter of debate. This review provides an update on recent clinicopathological and molecular data on lobular neoplasia and how these have changed the way these lesions are perceived and, most importantly, managed. Furthermore, the current recommendations for the management of lobular neoplasia diagnosed on core needle biopsies proposed in the National Health Service Breast Cancer Screening guidelines are discussed.

Keywords: lobular carcinoma in situ, atypical lobular hyperplasia, E‐cadherin, pleomorphic lobular carcinoma, β‐catenin

The first illustration of lobular neoplasia (LN) was published by Ewing, back in 1919, who described this lesion as an “atypical proliferation of acinar cells”.1 However, it was Foote and Steward, who, in 1941, first recognised this group of lesions as a distinct entity and coined the term “lobular carcinoma in situ” (LCIS).2 Although this seminal study was published more than 65 years ago, the main characteristics of the disease were accurately described. Indeed, most are still accepted, including that LCIS: (i) originates from cells in the terminal duct‐lobular unit or terminal ducts; (ii) is usually multicentric, often bilateral and not readily identifiable in gross examination; (iii) is composed of a monomorphic population of discohesive cells that expand the terminal duct‐lobular units and disseminate through the ductal system in a way that recalls Paget's disease (pagetoid spread, called “sandwich” pattern by Haagensen et al3); and (iv) is almost never seen in association with true Paget's disease of the nipple.2 Even the associations with its invasive counterpart, invasive lobular carcinoma, and other types of low grade breast cancer (i.e., low grade ductal/no special type and tubular carcinomas) were described in that seminal paper.2 The precursor nature of LN was also suggested by Muir, in 1941, who coined the term “intra‐acinous carcinoma” to refer to these lesions.

In 1978, Haagensen et al3 published their own series of 211 patients and reviewed the literature on “lobular carcinoma in situ” not associated with other forms of breast cancer. Their conclusions were largely in agreement with those of Foote and Stewart,2 however they considered the term “lobular carcinoma in situ”, when not associated with invasive cancer, a misnomer,3 given that the evidence available at that time suggested that those lesions were in fact a “benign, noninfiltrating, special microscopical form of lobular proliferation of the mammary epithelium”.3 They suggested the use of the term “lobular neoplasia” (LN) instead. This term was subsequently widely accepted and played an important role in changing the management of the lesion, from mastectomy to follow‐up. However, in hindsight, it is also arguable that this study,3 which called into question the precursor nature of this lesion, also delayed an understanding of the true biology and clinical behaviour of LN.

For a long time it has been debated whether LN is a non‐obligate breast cancer precursor, or a mere risk indicator.2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17 The risk indicator nature of LCIS is not in dispute; in fact, it is widely accepted that LCIS confers an increased risk of development of invasive carcinoma of about 1–2%/year, a 10‐year risk of 7–8%, a lifetime risk of 30–40% and a relative risk of breast cancer of 8–10.3,8,15,18 The term “atypical lobular hyperplasia” (ALH) was introduced to describe a morphologically similar but less well‐developed lesion (see below), which confers a relative risk of breast cancer development of 4–5.16,19,20

Although ALH and LCIS confer different relative risks of developing subsequent invasive breast cancer, distinguishing the two lesions is, at least partly, subjective. For some experts the differences between these two categories of lobular neoplasia are expressed more easily in words than in actual practice.13 Criteria for distinguishing the two are difficult to apply in some situations (e.g., core biopsies, when pagetoid spread only is present, when the LN involves another underlying lesion such as sclerosing adenosis). For these reasons, the term LN which encompasses both ALH and LCIS, has been accepted by many diagnostic pathologists.21 Of note, in the context of diagnostic core biopsies, the use of the term lobular neoplasia is recommended by the UK NHS BSP (National Health Service Breast Screening Programme) guidelines for non‐operative diagnostic procedures and reporting in breast cancer screening.52

LCIS is most frequently diagnosed in women aged between 40 and 55 years (less than 10% of patients with LN are postmenopausal).3,5 However, estimating the true incidence of LCIS is fraught with difficulty, given that, in the pre‐breast cancer screening programme era, the majority of cases used to be incidental findings in biopsy specimens taken for other lesions and not associated with specific clinical or radiological findings (i.e., LN does not form a mass and <50% of cases are associated with microcalcifications).2,3,5 Although it is reported that the incidence of LN in otherwise benign biopsy specimens ranges from 0.5% to 3.8%,3,4 an accurate assessment of the prevalence of LN in the general population is yet to be provided.

Consistent with the idea of LN being a risk indicator, early epidemiological studies suggested that a diagnosis of ALH/LCIS would confer an increased risk of developing invasive cancer anywhere in either breast and that the invasive breast cancer was not necessarily of lobular histology.3,8,22 However, it has recently been shown that this risk is higher in the ipsilateral breast and mainly at the site of the biopsied LN.10,13 Furthermore, when cases of pure LCIS (i.e., without associated ductal carcinoma in situ (DCIS)) are followed, the subsequent invasive tumour is almost uniformly of lobular histology.12,13

Histopathology of lobular neoplasia

Although there is still controversy regarding the clinical implications of a diagnosis of LN, its morphological characteristics are well known. According to the latest World Health Organization classification of breast tumours, lobular neoplasia is defined as a “proliferation of generally small and often loosely cohesive cells originating in the terminal duct‐lobular unit, with or without pagetoid involvement of terminal ducts”.21 Architecturally, these lesions are characterised by a variable enlargement of the acini, which are filled by a monomorphic population of small, rather discohesive, round, cuboidal or polygonal cells, with inconspicuous cytoplasm (fig 1A1A).). Intracytoplasmic vacuoles, sometimes containing a central eosinophilic dot, are not uncommonly found2,3,5,21 (fig 1B1B).). Although the classic variant is composed of monomorphic cells, some variability in the cytomorphology between different cases, and frequently within the same case, has been reported. Thus the cells of classic LN can be classified into two sub‐types, according to criteria laid down by Haagensen23 and revised by Sneige et al24: type A, which are characterised by bland and mildly discohesive cells, with scant cytoplasm and nuclei approx 1.5× the size of that of a lymphocyte; and type B cells, which characteristically have more abundant cytoplasm, slightly bigger nuclei (2× the size of a lymphocyte nucleus), mild to moderate nuclear atypia (still falling into nuclear grade 1 or 2) and indistinct or absent nucleoli. This system of cytological categorisation, has not, however, proven of value and does not have a direct correlation with development of cancer; it has thus become more of an academic exercise.25 Indeed, Haagensen et al3 suggested that this would be too simplistic a classification.

figure cp40642.f1
Figure 1 (A) Lobular carcinoma in situ: note the expansion of the terminal duct lobular unit by a monomorphic cell population. (B) High‐power magnification of lobular neoplasia highlighting the discohesiveness of neoplastic cells and the ...

The term ALH is used to refer to a partial involvement of acini by lobular neoplasia cells. According to Page et al,4,9,10,16,20 for a diagnosis of LCIS, more than half of the acini in an involved lobular unit must be filled and distended by the characteristic cells, leaving no central lumina. However, the differences between ALH and LCIS at the morphological level (and molecular level, see below) appear to be merely quantitative with an arbitrarily set threshold; therefore, it is not surprising that there is a great degree of inter‐ and intra‐observer variability in the differentiation between LCIS and ALH. Despite the morphological and molecular evidence to suggest that the differences between ALH and LCIS are negligible and the difficulties with reproducibility of diagnosis, given the acknowledged and significantly higher relative risk of breast cancer development associated with LCIS,4,9,10,16,19,20 the value of the terms ALH, LCIS and LN remains controversial. As noted above, in the context of diagnostic core biopsy specimens, where limited sampling is a significant issue, the use of the term lobular neoplasia should be used as per the UK NHS BSP guidelines for non‐operative diagnostic procedures and reporting in breast cancer screening.52

More biologically and clinically important is the recognition of the recently described pleomorphic variant of lobular carcinoma in situ, which was first identified as a distinct entity by Eusebi et al26 in 1992. In 2002, the first detailed analysis of pleomorphic LCIS not associated with invasive cancer was reported.24 Pleomorphic LCIS is characterised by cells that are remarkably bigger than those of classic LN, have more abundant, pink and finely granular cytoplasm, frequently display features of apocrine differentiation and harbour more pleomorphic, atypical nuclei, with conspicuous nucleoli24,26,27 (fig 22).). Central, comedo‐type necrosis and microcalcifications are not uncommon in this variant. It is almost certain that some of these lesions were classified as high grade DCIS, in the past.24,27 Other variants of LN are also on record, including endocrine, amphicrine, apocrine, histiocytoid, rhabdoid and the pleomorphic apocrine LCIS variant28,29; however, their biological and/or clinical significance remains uncertain.

figure cp40642.f2
Figure 2 Pleomorphic lobular carcinoma in situ associated with invasive pleomorphic lobular carcinoma. (A and B) Low power magnification of a rather extensive lesions with multiple areas of comedo necrosis. (C) Coarse microcalcifications are not ...

Ancillary immunohistochemical markers

Lobular neoplasia consistently shows positivity for oestrogen and progesterone receptors; even the pleomorphic variant is reported to show expression of these markers in >90% of cases.5,24,27,30 However, some differences in the expression of classic biomarkers of aggressiveness have been observed between the classic and pleomorphic variants (table 11).). While expression of p53 and HER2 is remarkably rare in classic LN, p53 expression (as defined by >10% of neoplastic cells) and HER2 overexpression are found in approximately 30% of pleomorphic LCIS.5,24,27,30 Furthermore, HER2 gene amplification and high MIB‐1 labelling indices have been reported in the pleomorphic variant, while these are not features of classic LN.5,24,27,30 Given the high frequency of apocrine differentiation in the pleomorphic variant, it is not surprising that >60% of pleomorphic LCIS shows expression of gross cystic disease fluid protein‐15,26,30 a marker of apocrine differentiation.

Table thumbnail
Table 1 Summary of ancillary markers for the diagnosis of lobular neoplasia

In recent years, the likeliest underlying molecular mechanism for the discohesiveness so typical of LN has been identified. There are several lines of evidence to suggest that this is due to a lack, or a significant reduction, of the expression of functional E‐cadherin.5,31,32,33,34,35,36,37,38,39,40,41,42,43,44 This protein mediates homophylic‐homotypic adhesions and is consistently expressed, as a membrane marker, in luminal epithelial cells of the breast. Both classic and pleomorphic variants of LN fail to express this protein in >95% of cases,5,31,32,33,34,35,36,37,38,39,40,41,42,43,44 and some have reported that focal expression of this protein may be associated with higher recurrence rates.45,46

E‐cadherin has been used as a successful marker to differentiate ductal from lobular proliferations.41,42,43,44 In fact, some authorities have suggested that solid in situ proliferations with indeterminate features are best classified according to the pattern of E‐cadherin expression: those with E‐cadherin expression should be considered DCIS, whereas cases that lack the expression of this adhesion molecule are best classified as LN41,42,43,44 (fig 33).). In addition, some cases of carcinomas in situ with indeterminate features may harbour a mixed pattern of E‐cadherin expression and should be classified as mixed lesions.43 Interestingly, molecular data in support of this approach have recently been published.27

figure cp40642.f3
Figure 3 (A) Carcinoma in situ with indeterminate features. (B) Lack of E‐cadherin staining helps classify these lesions as variants of lobular neoplasia.

High molecular weight cytokeratins identified by the clone 34βE12 (i.e., cytokeratins 1, 5, 10 and 14) were reported to be consistently expressed in LN and it has been suggested that this antibody could be used to differentiate it from ductal lesions.44 However, there is strong evidence to suggest that LN cells do not express cytokeratins 1, 5, 10 and 14 and that 34βE12 positivity in LN may be an artefact of antigen retrieval.47 In addition, up to 15% of ductal carcinomas may express basal keratins,48 and low‐grade ductal/no special type and tubular neoplasms are also reported to show positivity for 34βE12.49 Therefore, we would recommend caution when using the 34βE12 for a diagnosis of lobular neoplasia.

More recently, other proteins that form complexes with E‐cadherin have been successfully used to differentiate between ductal and lobular neoplasms. These new markers include β‐ and α‐catenin,39 which are also lost in the majority of LNs, and p120 cadherin,50 which is expressed in the membrane of non‐neoplastic luminal cells and ductal proliferations, and shows cytoplasmic rather than membranous expression in LN. Of note, this expression pattern is present from the early stages of lobular breast cancer but is maintained during tumour progression and is seen in metastatic deposits. However, further studies are required to accurately define the use of these ancillary markers to differentiate LN from its mimics.

Differential diagnosis

The main pitfalls that can pose problems in the identification of LN have been described elsewhere.28,51 Poor tissue fixation, not uncommonly seen in mastectomy specimens, can lead to an artefactual appearance of discohesion within a lobular unit, resulting in an overdiagnosis of LCIS. Fortunately, this is an infrequent problem in diagnostic core biopsy specimens. It should be noted that in core biopsy samples the pathologist should not strive to distinguish ALH from LCIS52; their categorisation lies in an assessment of the extent and degree of expansion of lobular units, which is not possible in the limited amount of tissue often received. The lesion in a core biopsy specimen should be diagnosed as LN and classified as B3, of uncertain malignant potential, and multidisciplinary discussion should take place.

Differentiating low grade, solid DCIS from LN is, sometimes, an exceedingly difficult task,41,42,43,44 even in surgical excisional samples. In cases of carcinoma in situ with indeterminate features, it has been suggested that the presence of a mosaic growth pattern with prominent intracytoplasmic vacuoles is more suggestive of LN, whereas the presence of microacinar‐like structures would favour a diagnosis of solid low‐grade DCIS.43 However, as discussed above, in this context E‐cadherin staining is particularly helpful.41,42,43,44 Nevertheless it may simply not be possible to unequivocally distinguish LN from low grade DCIS in limited core biopsy specimens; such a lesion can be classified as B4, suspicious, and further investigations such as repeat (11 gauge) biopsy or diagnostic surgery undertaken.

In the non‐operative setting in particular, the other important differential diagnosis of LN is cancerisation of the lobules by DCIS. Cancerisation of the lobules by DCIS is a well known phenomenon, which was included in the definition of “intra‐acinous carcinoma” by Muir.6 In fact, that author failed to appreciate that LN and cancerisation of the lobules were distinct pathological processes and stated that “intra‐acinous carcinoma is often merely the result of the spread of cancer cells from terminal ducts in which the malignant process has started”. However, since Fechner's report53 on this phenomenon, it has become clear that LN and cancerisation of the lobules are completely separate entities and should be differentiated. This phenomenon is particularly troublesome in cases where the differential diagnosis is between lobular cancerisation and pleomorphic LCIS. Again, immunohistochemistry with anti‐E‐cadherin antibodies is helpful; a lack of membranous E‐cadherin staining would strongly militate against a diagnosis of cancerisation of the lobules by high grade DCIS.

It is also important to remember that benign lesions in core biopsy specimens may sometimes be misleading; for instance, foci of clear cell metaplasia or lactational change containing intracytoplasmic lipid droplets may bear some resemblance to ALH/LCIS. LN is not infrequently seen in association with coexisting benign lesions, including radial scar, sclerosing adenosis and fibroadenoma (fig 44),), which clinically and radiologically may present as a mass. The histological appearance of LN in association with these lesions may cause difficulties for the unwary.

figure cp40642.f4
Figure 4 Troublesome cases of lobular neoplasia. (A) Lobular neoplasia arising in sclerosing adenosis. (B) Note the continuous layer of calponin‐positive, myoepithelial cells. (C) Lobular neoplasia arising in a fibroadenoma. (D) Neoplastic ...

Molecular pathology

Molecular genetic studies have provided a wealth of increasingly more coherent data on the pathways of breast cancer evolution and how these findings correlate with morphological features. It is currently believed that at the molecular genetic level, breast cancer can be classified into two groups. The low grade group is characterised by low nuclear grade, consistent positivity for oestrogen and progesterone receptors, lack of HER2 overexpression and, at the genetic level, quite simple, diploid or near diploid karyotypes. The most frequent genomic changes in lesions of this group comprise deletions of 16q, and gains of 1p and 16p.54 High grade lesions are characterised by much more complex karyotypes, which are frequently aneuploid. Although these lesions have many more unbalanced genomic changes, deletions of the whole 16q arm are seen in <10% of these cases. Even when these are present, they are reported to occur through distinct genetic mechanisms,55 suggesting that progression from low to high grade breast cancers is an unlikely, or at least a rare, phenomenon.54,55

Conversely, the molecular data have blurred the boundaries between low‐grade ductal and lobular proliferations. These lesions have remarkably similar immunohistochemical and molecular genetic profiles, the main difference being the target gene of 16q deletions.34,56,57 While in low‐grade ductal lesions the target gene remains as yet unidentified,34,56,57,58 in LN it has been shown to be the CDH1 gene, which encodes E‐cadherin. The CDH1 gene is reported to be inactivated in both LCIS and invasive lobular cancer (ILC), through a variable combination of genetic (deletions and inactivating mutations) and epigenetic (gene promoter methylation) mechanisms.32,33 In addition, Vos et al36 have shown concurrent identical truncating mutations in the E‐cadherin gene in matched LCIS and adjacent ILC. Noteworthy, although CDH1 mutations appear to be more frequent in LCIS, they have even been found in ALH not associated with invasive cancer.39 On the other hand, comprehensive surveys of low grade ductal carcinomas have failed to identify CDH1 truncating gene mutations or E‐cadherin down‐regulation.5,36,42,43,44,56,58 Another level of evidence linking CDH1 gene inactivation and LN comes from studies of families with CDH1 germline mutations, who are reported to have a remarkably high risk of development of signet ring gastric cancer and lobular carcinoma.59 More recently, by introducing conditional cdh1 gene mutations into a conditional mouse tumour model based on epithelium‐specific knockout of p53, Derksen et al have shown that E‐cadherin inactivation leads to the genesis of neoplasms morphologically identical to human invasive lobular carcinomas.60 Taken together, these data provide strong evidence to suggest that LCIS is a non‐obligate precursor of ILC and that CDH1 gene inactivation is paramount for the pathogenesis of lobular lesions.

Comparative genomic hybridisation (CGH) analysis of LN has shown that ALH and LCIS harbour strikingly similar unbalanced chromosomal changes, with the most frequent aberrations comprising deletions of 16p, 16q, 17p, and 22q and gains of 6q.61 Interestingly, more recent chromosomal62,63 and microarray‐based40,64,65 CGH studies have shown that deletions of 16q, 8ptel‐p12 and 11q14‐qtel and gains of 1q, 8p12‐p11.2, 11q13 and 16p are the most frequent molecular genetic changes found in lobular carcinoma. Most importantly, array CGH and mitochondrial DNA analyses have confirmed the similarities between matched LN and ILC at the molecular genetic level,64,66 providing additional, circumstantial evidence in support of a precursor role for LN.

Although molecular data on the pleomorphic variant are scant, deletions of 16q, mapping to the CDH1 gene locus have been shown.67 In a recent study, a case of matched pleomorphic LCIS and invasive pleomorphic lobular carcinoma revealed remarkably similar molecular genetic profiles, with a similarity of 72%, as defined by high resolution CGH and a correlation index of 0.784 as assessed by microarray‐based CGH.27 Furthermore, it is now well accepted that pleomorphic LCIS harbours the hallmark genetic features of LN, namely gain of 1q and deletion of 16q coupled with E‐cadherin inactivation. However, pleomorphic LCIS has proven to be a genetically advanced lesion, with complex karyotypes. Amplification of HER2 and MYC, gain of 20q and deletion of 13q may account for the high grade nuclear features and the reported more aggressive behaviour of this variant.27

Management of lobular neoplasia in core needle biopsy specimens

Contrary to initial descriptions,2,3,23 LN is reported to be associated with microcalcifications in up to 40% of cases diagnosed on core needle biopsy (CNB).68,69,70 However, LN is infrequently seen as the sole diagnostic finding in such specimens, accounting for 0.5–2.9% of biopsy specimens taken for histological assessment of mammography detected lesions.70,71,72,73,74,75,76,77,78,79,80,69 There is a paucity of peer reviewed data and prospective analyses on this topic in the literature; most management recommendations have therefore been based more on pragmatism than scientific evidence. Until recently,5,69 most authors agreed that excision should be performed in cases of LN diagnosed on a CNB in the following instances: (i) another lesion, which would itself be an indication for surgical excision, was also present on the core biopsy (such as ADH or a radial scar); (ii) there was discordance between clinical, radiological and pathological findings; (iii) there was an associated mass lesion or an area of architectural distortion; (iv) the ALH or LCIS showed mixed histological features with difficulty in distinguishing the lesion from DCIS, or showed a mixed E‐cadherin staining pattern; and (v) the morphology was consistent with that of the pleomorphic variant of lobular neoplasia.51,69

The above method of selection of cases that should undergo further assessment has not been universally applied; some UK breast units have been recommending and undertaking surgical diagnostic surgical excision of all LN for many years,71 while other groups have been excising only those cases defined as above, and in particular those with radiological/surgical/pathological discordance. In the last two years, North American authors have suggested that LN should be perceived as “high‐risk” and recommended excision of all cases due to the underestimation of cancer in up to 33% of LN diagnosed on CNB.78,79

In summary, while it is of utmost importance to avoid unnecessary diagnostic surgery for patients where LN is the sole finding in a core biopsy specimen, the risk of associated malignancy in the adjacent breast at the time of diagnosis should be noted. Some have advocated that a multidisciplinary approach for such cases is essential81 and that each case must be assessed individually. Although there is a paucity of large prospective studies to define accurately the risk of underestimating the presence of more aggressive lesions in patients where classic LN is the sole diagnosis in a core biopsy specimen, based on the evidence currently available we would recommend diagnostic surgical excision of all such lesions. Despite the rather limited data on the pleomorphic variant of LN, there is circumstantial evidence to suggest that these lesions are more frequently associated higher risk lesions and may have a more aggressive clinical behaviour than classic LN; therefore, many would recommend that such cases should subjected to further excision.

Take‐home messages

  • Lobular neoplasia is both a risk indicator and a non‐obligate precursor of invasive breast cancer.
  • In core biopsies, atypical lobular hyperplasia and lobular carcinoma in situ should be diagnosed as lobular neoplasia and classified as B3.
  • E‐cadherin, B‐catenin and p120 catenin are useful markers to differentiate lobular from ductal proliferations.
  • Pleomorphic lobular carcinoma in situ is a high grade and more aggressive variant of lobular neoplasia.

Abbreviations

ADH - atypical ductal hyperplasia

ALH - atypical lobular hyperplasia

CGH - comparative genomic hybridisation

CNB - core needle biopsy

DCIS - ductal carcinoma in situ

ILC - invasive lobular cancer

LCIS - lobular carcinoma in situ

LN - lobular neoplasia

Footnotes

Competing interests: None declared.

References

1. Ewing J. Neoplastic diseases: a textbook on tumors. Philadelphia, PA: WB Saunders, 1919
2. Foote F W, Stewart F W. Lobular carcinoma in situ: a rare form of mammary carcinoma. Am J Pathol 1941. 17491–499.499 [PMC free article] [PubMed]
3. Haagensen C D, Lane N, Lattes R. et al Lobular neoplasia (so‐called lobular carcinoma in situ) of the breast. Cancer 1978. 42737–769.769 [PubMed]
4. Page D L, Kidd T E, Jr, Dupont W D. et al Lobular neoplasia of the breast: higher risk for subsequent invasive cancer predicted by more extensive disease. Hum Pathol 1991. 221232–1239.1239 [PubMed]
5. Simpson P T, Gale T, Fulford L G. et al The diagnosis and management of pre‐invasive breast disease: pathology of atypical lobular hyperplasia and lobular carcinoma in situ. Breast Cancer Res 2003. 5258–262.262 [PMC free article] [PubMed]
6. Muir R. The evolution of carcinoma of the mamma. J Pathol Bacteriol 1941. 52155–172.172
7. Rieger‐Christ K M, Pezza J A, Dugan J M. et al Disparate E‐cadherin mutations in LCIS and associated invasive breast carcinomas. Mol Pathol 2001. 5491–97.97 [PMC free article] [PubMed]
8. Chuba P J, Hamre M R, Yap J. et al Bilateral risk for subsequent breast cancer after lobular carcinoma‐in‐situ: analysis of surveillance, epidemiology, and end results data. J Clin Oncol 2005. 235534–5541.5541 [PubMed]
9. Page D L, Simpson J F. What is atypical lobular hyperplasia and what does it mean for the patient? J Clin Oncol 2005. 235432–5433.5433 [PubMed]
10. Page D L, Schuyler P A, Dupont W D. et al Atypical lobular hyperplasia as a unilateral predictor of breast cancer risk: a retrospective cohort study. Lancet 2003. 361125–129.129 [PubMed]
11. Lakhani S R. In‐situ lobular neoplasia: time for an awakening. Lancet 2003. 36196 [PubMed]
12. Maluf H, Koerner F. Lobular carcinoma in situ and infiltrating ductal carcinoma: frequent presence of DCIS as a precursor lesion. Int J Surg Pathol 2001. 9127–131.131 [PubMed]
13. Fisher E R, Land S R, Fisher B. et al Pathologic findings from the National Surgical Adjuvant Breast and Bowel Project: twelve‐year observations concerning lobular carcinoma in situ. Cancer 2004. 100238–244.244 [PubMed]
14. Fisher E R, Costantino J, Fisher B. et al Pathologic findings from the National Surgical Adjuvant Breast Project (NSABP) Protocol B‐17. Five‐year observations concerning lobular carcinoma in situ. Cancer 1996. 781403–1416.1416 [PubMed]
15. Andersen J A. Lobular carcinoma in situ of the breast. An approach to rational treatment. Cancer 1977. 392597–2602.2602 [PubMed]
16. McLaren B K, Schuyler P A, Sanders M E. et al Excellent survival, cancer type, and Nottingham grade after atypical lobular hyperplasia on initial breast biopsy. Cancer 2006. 1071227–1233.1233 [PubMed]
17. Lattes R. Lobular neoplasia (lobular carcinoma in situ) of the breast—a histological entity of controversial clinical significance. Pathol Res Pract 1980. 166415–429.429 [PubMed]
18. Bauer T L, Pandelidis S M, Rhoads J E., Jr Five‐year survival of 100 women with carcinoma of the breast diagnosed by screening mammography and needle‐localization biopsy. J Am Coll Surg 1994. 178427–430.430 [PubMed]
19. Page D L, Dupont W D, Rogers L W. Ductal involvement by cells of atypical lobular hyperplasia in the breast: a long‐term follow‐up study of cancer risk. Hum Pathol 1988. 19201–207.207 [PubMed]
20. Page D L, Dupont W D, Rogers L W. et al Atypical hyperplastic lesions of the female breast. A long‐term follow‐up study. Cancer 1985. 552698–2708.2708 [PubMed]
21. Tavassoli F A, Hoefler H, Rosai J. et al Intraductal proliferative lesions. In: Tavassoli FA, Devilee P, eds. Pathology & genetics tumours of the breast and female genital organs. Lyon: IARC Press, 2003
22. Haagensen C D, Lane N, Bodian C. Coexisting lobular neoplasia and carcinoma of the breast. Cancer 1983. 511468–1482.1482 [PubMed]
23. Haagensen C D. Diseases of the breast. Philadelphia, PA: WB Saunders, 1971
24. Sneige N, Wang J, Baker B A. et al Clinical, histopathologic, and biologic features of pleomorphic lobular (ductal‐lobular) carcinoma in situ of the breast: a report of 24 cases. Mod Pathol 2002. 151044–1050.1050 [PubMed]
25. Wheeler J E, Enterline H T, Roseman J M. et al Lobular carcinoma in situ of the breast. Long‐term follow up. Cancer 1974. 34554–563.563 [PubMed]
26. Eusebi V, Magalhaes F, Azzopardi J G. Pleomorphic lobular carcinoma of the breast: an aggressive tumor showing apocrine differentiation. Hum Pathol 1992. 23655–662.662 [PubMed]
27. Reis‐Filho J S, Simpson P T, Jones C. et al Pleomorphic lobular carcinoma of the breast: role of comprehensive molecular pathology in characterization of an entity. J Pathol 2005. 2071–13.13 [PubMed]
28. Koerner F, Maluf H. Uncommon morphologic patterns of lobular neoplasia. Ann Diagn Pathol 1999. 3249–259.259 [PubMed]
29. Chen Y, Fitzgibbons P, Jacobs T. et al Pleomorphic apocrine lobular carcinoma in situ (PALCIS): phenotypic and genetic study of a distinct‐variant of lobular carcinoma in situ (LCIS). Lab Invest 2005. 8529A
30. Frolik D, Caduff R, Varga Z. Pleomorphic lobular carcinoma of the breast: its cell kinetics, expression of oncogenes and tumour suppressor genes compared with invasive ductal carcinomas and classical infiltrating lobular carcinomas. Histopathology 2001. 39503–513.513 [PubMed]
31. Gamallo C, Palacios J, Suarez A. et al Correlation of E‐cadherin expression with differentiation grade and histological type in breast carcinoma. Am J Pathol 1993. 142987–993.993 [PMC free article] [PubMed]
32. Sarrio D, Moreno‐Bueno G, Hardisson D. et al Epigenetic and genetic alterations of APC and CDH1 genes in lobular breast cancer: relationships with abnormal E‐cadherin and catenin expression and microsatellite instability. Int J Cancer 2003. 106208–215.215 [PubMed]
33. Droufakou S, Deshmane V, Roylance R. et al Multiple ways of silencing E‐cadherin gene expression in lobular carcinoma of the breast. Int J Cancer 2001. 92404–408.408 [PubMed]
34. Cleton‐Jansen A M. E‐cadherin and loss of heterozygosity at chromosome 16 in breast carcinogenesis: different genetic pathways in ductal and lobular breast cancer? Breast Cancer Res 2002. 45–8.8 [PMC free article] [PubMed]
35. De Leeuw W J, Berx G, Vos C B. et al Simultaneous loss of E‐cadherin and catenins in invasive lobular breast cancer and lobular carcinoma in situ. J Pathol 1997. 183404–411.411 [PubMed]
36. Vos C B, Cleton‐Jansen A M, Berx G. et al E‐cadherin inactivation in lobular carcinoma in situ of the breast: an early event in tumorigenesis. Br J Cancer 1997. 761131–1133.1133 [PMC free article] [PubMed]
37. Berx G, Cleton‐Jansen A M, Strumane K. et al E‐cadherin is inactivated in a majority of invasive human lobular breast cancers by truncation mutations throughout its extracellular domain. Oncogene 1996. 131919–1925.1925 [PubMed]
38. Berx G, Cleton‐Jansen A M, Nollet F. et al E‐cadherin is a tumour/invasion suppressor gene mutated in human lobular breast cancers. Embo J 1995. 146107–6115.6115 [PMC free article] [PubMed]
39. Mastracci T L, Tjan S, Bane A L. et al E‐cadherin alterations in atypical lobular hyperplasia and lobular carcinoma in situ of the breast. Mod Pathol 2005. 18741–751.751 [PubMed]
40. Reis‐Filho J S, Simpson P T, Turner N C. et al FGFR1 emerges as a potential therapeutic target for labular breast carcinomas. Clin Cancer Res 2006. 126652–6662.6662 [PubMed]
41. Maluf H M. Differential diagnosis of solid carcinoma in situ. Semin Diagn Pathol 2004. 2125–31.31 [PubMed]
42. Maluf H M, Swanson P E, Koerner F C. Solid low‐grade in situ carcinoma of the breast: role of associated lesions and E‐cadherin in differential diagnosis. Am J Surg Pathol 2001. 25237–244.244 [PubMed]
43. Jacobs T W, Pliss N, Kouria G. et al Carcinomas in situ of the breast with indeterminate features: role of E‐cadherin staining in categorization. Am J Surg Pathol 2001. 25229–236.236 [PubMed]
44. Bratthauer G L, Moinfar F, Stamatakos M D. et al Combined E‐cadherin and high molecular weight cytokeratin immunoprofile differentiates lobular, ductal, and hybrid mammary intraepithelial neoplasias. Hum Pathol 2002. 33620–627.627 [PubMed]
45. Goldstein N S, Kestin L L, Vicini F A. Clinicopathologic implications of E‐cadherin reactivity in patients with lobular carcinoma in situ of the breast. Cancer 2001. 92738–747.747 [PubMed]
46. Reis‐Filho J S, Cancela Paredes J, Milanezi F. et al Clinicopathologic implications of E‐cadherin reactivity in patients with lobular carcinoma in situ of the breast. Cancer 2002. 942114–2116.2116 [PubMed]
47. Bratthauer G L, Miettinen M, Tavassoli F A. Cytokeratin immunoreactivity in lobular intraepithelial neoplasia. J Histochem Cytochem 2003. 511527–1531.1531 [PMC free article] [PubMed]
48. Abd El‐Rehim D M, Pinder S E, Paish C E. et al Expression of luminal and basal cytokeratins in human breast carcinoma. J Pathol 2004. 203661–671.671 [PubMed]
49. Wheeler D T, Tai L H, Bratthauer G L. et al Tubulolobular carcinoma of the breast: an analysis of 27 cases of a tumor with a hybrid morphology and immunoprofile. Am J Surg Pathol 2004. 281587–1593.1593 [PubMed]
50. Sarrio D, Perez‐Mies B, Hardisson D. et al Cytoplasmic localization of p120ctn and E‐cadherin loss characterize lobular breast carcinoma from preinvasive to metastatic lesions. Oncogene 2004. 233272–3283.3283 [PubMed]
51. Fulford L G, Reis‐Filho J S, Lakhani S R. Lobular in situ neoplasia. Curr Diagn Pathol 2004. 10183–192.192
52. NHS Guidelines for non‐operative diagnostic procedures and reporting in breast cancer screening. NHS BSP Publication No 50. Sheffield: NHS BSP, 2001
53. Fechner R E. Ductal carcinoma involving the lobule of the breast. A source of confusion with lobular carcinoma in situ. Cancer 1971. 28274–281.281 [PubMed]
54. Simpson P T, Reis‐Filho J S, Gale T. et al Molecular evolution of breast cancer. J Pathol 2005. 205248–254.254 [PubMed]
55. Cleton‐Jansen A M, Buerger H, Haar N. et al Different mechanisms of chromosome 16 loss of heterozygosity in well versus poorly differentiated ductal breast cancer. Genes Chromosomes Cancer 2004. 41109–116.116 [PubMed]
56. van Wezel T, Lombaerts M, van Roon E H. et al Expression analysis of candidate breast tumour suppressor genes on chromosome 16q. Breast Cancer Res 2005. 7R998–1004.1004 [PMC free article] [PubMed]
57. Rakha E A, Green A R, Powe D G. et al Chromosome 16 tumor‐suppressor genes in breast cancer. Genes Chromosomes Cancer 2006. 45527–535.535 [PubMed]
58. Roylance R, Droufakou S, Gorman P. et al The role of E‐cadherin in low‐grade ductal breast tumourigenesis. J Pathol 2003. 20053–58.58 [PubMed]
59. Brooks‐Wilson A R, Kaurah P, Suriano G. et al Germline E‐cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria. J Med Genet 2004. 41508–517.517 [PMC free article] [PubMed]
60. Derksen P W, Liu X, Saridin F. et al Somatic inactivation of E‐cadherin and p53 in mice leads to metastatic lobular mammary carcinoma through induction of anoikis resistance and angiogenesis. Cancer Cell 2006. 10437–449.449 [PubMed]
61. Lu Y J, Osin P, Lakhani S R. et al Comparative genomic hybridization analysis of lobular carcinoma in situ and atypical lobular hyperplasia and potential roles for gains and losses of genetic material in breast neoplasia. Cancer Res 1998. 584721–4727.4727 [PubMed]
62. Buerger H, Simon R, Schafer K L. et al Genetic relation of lobular carcinoma in situ, ductal carcinoma in situ, and associated invasive carcinoma of the breast. Mol Pathol 2000. 53118–121.121 [PMC free article] [PubMed]
63. Etzell J E, Devries S, Chew K. et al Loss of chromosome 16q in lobular carcinoma in situ. Hum Pathol 2001. 32292–296.296 [PubMed]
64. Shelley Hwang E, Nyante S J, Yi Chen Y. et al Clonality of lobular carcinoma in situ and synchronous invasive lobular carcinoma. Cancer 2004. 1002562–2572.2572 [PubMed]
65. Loo L W, Grove D I, Williams E M. et al Array comparative genomic hybridization analysis of genomic alterations in breast cancer subtypes. Cancer Res 2004. 648541–8549.8549 [PubMed]
66. Morandi L, Marucci G, Foschini M P. et al Genetic similarities and differences between lobular in situ neoplasia (LN) and invasive lobular carcinoma of the breast. Virchows Arch 2006. 44914–23.23 [PubMed]
67. Palacios J, Sarrio D, Garcia‐Macias M C. et al Frequent E‐cadherin gene inactivation by loss of heterozygosity in pleomorphic lobular carcinoma of the breast. Mod Pathol 2003. 16674–678.678 [PubMed]
68. Middleton L P, Grant S, Stephens T. et al Lobular carcinoma in situ diagnosed by core needle biopsy: when should it be excised? Mod Pathol 2003. 16120–129.129 [PubMed]
69. Jacobs T W, Connolly J L, Schnitt S J. Nonmalignant lesions in breast core needle biopsies: to excise or not to excise? Am J Surg Pathol 2002. 261095–1110.1110 [PubMed]
70. Crisi G M, Mandavilli S, Cronin E. et al Invasive mammary carcinoma after immediate and short‐term follow‐up for lobular neoplasia on core biopsy. Am J Surg Pathol 2003. 27325–333.333 [PubMed]
71. O'Driscoll D, Britton P, Bobrow L. et al Lobular carcinoma in situ on core biopsy—what is the clinical significance? Clin Radiol 2001. 56216–220.220 [PubMed]
72. Shin S J, Rosen P P. Excisional biopsy should be performed if lobular carcinoma in situ is seen on needle core biopsy. Arch Pathol Lab Med 2002. 126697–701.701 [PubMed]
73. Renshaw A A, Derhagopian R P, Martinez P. et al Lobular neoplasia in breast core needle biopsy specimens is associated with a low risk of ductal carcinoma in situ or invasive carcinoma on subsequent excision. Am J Clin Pathol 2006. 126310–313.313 [PubMed]
74. Renshaw A A, Cartagena N, Derhagopian R P. et al Lobular neoplasia in breast core needle biopsy specimens is not associated with an increased risk of ductal carcinoma in situ or invasive carcinoma. Am J Clin Pathol 2002. 117797–799.799 [PubMed]
75. Renshaw A A, Cartagena N, Schenkman R H. et al Atypical ductal hyperplasia in breast core needle biopsies. Correlation of size of the lesion, complete removal of the lesion, and the incidence of carcinoma in follow‐up biopsies. Am J Clin Pathol 2001. 11692–96.96 [PubMed]
76. Bauer V P, Ditkoff B A, Schnabel F. et al The management of lobular neoplasia identified on percutaneous core breast biopsy. Breast J 2003. 94–9.9 [PubMed]
77. Dmytrasz K, Tartter P I, Mizrachy H. et al The significance of atypical lobular hyperplasia at percutaneous breast biopsy. Breast J 2003. 910–12.12 [PubMed]
78. Elsheikh T M, Silverman J F. Follow‐up surgical excision is indicated when breast core needle biopsies show atypical lobular hyperplasia or lobular carcinoma in situ: a correlative study of 33 patients with review of the literature. Am J Surg Pathol 2005. 29534–543.543 [PubMed]
79. Mahoney M C, Robinson‐Smith T M, Shaughnessy E A. Lobular neoplasia at 11‐gauge vacuum‐assisted stereotactic biopsy: correlation with surgical excisional biopsy and mammographic follow‐up. AJR Am J Roentgenol 2006. 187949–954.954 [PubMed]
80. Liberman L, Sama M, Susnik B. et al Lobular carcinoma in situ at percutaneous breast biopsy: surgical biopsy findings. AJR Am J Roentgenol 1999. 173291–299.299 [PubMed]
81. Lee A H, Denley H E, Pinder S E. et al Excision biopsy findings of patients with breast needle core biopsies reported as suspicious of malignancy (B4) or lesion of uncertain malignant potential (B3). Histopathology 2003. 42331–336.336 [PubMed]

Articles from Journal of Clinical Pathology are provided here courtesy of BMJ Group
PubReader format: click here to try

Formats:

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...

Links

  • MedGen
    MedGen
    Related information in MedGen
  • PubMed
    PubMed
    PubMed citations for these articles

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...