Pathology of breast cancer (uptodate, 2017) | ПРЕЦИЗИОННАЯ ОНКОЛОГИЯ

Pathology of breast cancer (uptodate, 2017)


Most breast malignancies arise from epithelial elements and are categorized as carcinomas. Breast carcinomas are a diverse group of lesions that differ in microscopic appearance and biologic behavior, although these disorders are often discussed as a single disease.

The in situ carcinomas of the breast are either ductal (also known as intraductal carcinoma) or lobular. This distinction is primarily based upon the growth pattern and cytologic features of the lesions, rather than their anatomic location within the mammary ductal-lobular system.

The invasive breast carcinomas consist of several histologic subtypes; the estimated%ages are from a contemporary population-based series of 135,157 women with breast cancer reported to the Surveillance, Epidemiology, and End Results (SEER) database of the National Cancer Institute between 1992 and 2001 [1]:

  • Infiltrating ductal – 76%
  • Invasive lobular – 8%
  • Ductal/lobular – 7%
  • Mucinous (colloid) – 2.4%
  • Tubular – 1.5%
  • Medullary – 1.2%
  • Papillary – 1%

Other subtypes, including metaplastic breast cancer and invasive micropapillary breast cancer, all account for less than 5% of cases [2].

This topic will review the histology of ductal carcinoma in situ and invasive breast carcinoma. The pathologies of atypical hyperplasia, lobular carcinoma in situ, and other subtypes of breast cancer are discussed separately.


The term ductal carcinoma in situ (DCIS) encompasses a heterogeneous group of lesions that differ in their clinical presentation, histologic appearance, and biologic potential. DCIS is characterized by proliferation of presumably malignant epithelial cells within the mammary ductal system, with no evidence of invasion into the surrounding stroma on routine light microscopic examination [3]. Ductal carcinoma in situ differs from lobular carcinoma in situ with regard to radiologic features, morphology, biologic behavior, and anatomic distribution in the breast (table 1). Lobular carcinoma in situ is discussed in detail elsewhere.

Classification schemes that divide DCIS histologically into a variety of subtypes emphasize architectural features or growth pattern of the neoplastic cells, cytologic features, and cell necrosis, both singly and in combination. The traditional method for classifying DCIS lesions is primarily based upon the growth pattern (architectural features) of the tumor and recognizes five major types [4-7]:

  • The comedo type is characterized by prominent necrosis in the center of the involved spaces. The necrotic material frequently becomes calcified; the calcifications may be detected mammographically, characteristically as linear, branching («casting») calcifications. The tumor cells are large and show nuclear pleomorphism; mitotic activity may be prominent (picture 1). The comedo type is more often associated with invasion [8,9], and the degree of comedo necrosis in patients with DCIS appears to be a strong predictor for the risk of ipsilateral breast recurrence after treatment [10].
  • The cribriform type is characterized by the formation of back to back glands without intervening stroma. The cells comprising this subtype are typically small to medium sized and have relatively uniform hyperchromatic nuclei. Mitoses are infrequent, and necrosis is limited to single cells or small cell clusters (picture 2).
  • The micropapillary type features small tufts of cells that are oriented perpendicular to the basement membrane of the involved spaces and project into the lumina. The apical region of these small papillations is frequently broader than the base, imparting a club-shaped appearance. The micropapillae lack fibrovascular cores. The cells comprising this type of DCIS are usually small to medium in size, and the nuclei show diffuse hyperchromasia; mitoses are infrequent (picture 3).
  • The papillary type shows intraluminal projections of tumor cells that, in contrast to the micropapillary variant, demonstrate fibrovascular cores and thereby constitute true papillations. A variant of papillary DCIS, intracystic papillary carcinoma, is characterized by tumor cells that are primarily or exclusively present in a single cystically dilated space [11].
  • The solid type is not as well defined as the other subtypes. It features tumor cells that fill and distend the involved spaces and lack significant necrosis, fenestrations, or papillations. The tumor cells may be large, medium, or small.

Less common variants of DCIS include the «clinging» carcinoma [4], intraductal signet ring cell carcinoma [12], and cystic hypersecretory duct carcinoma [13,14]. Similar to the comedo type, these variants may show calcifications that can be detected mammographically. However, the mammographic appearance of these microcalcifications is less distinctive than the pattern seen in comedo lesions and can resemble a number of benign processes.

A number of authors have proposed alternative classification systems for DCIS (table 2) [15-18]. Although they use different terminology, all are primarily based upon nuclear grade and/or the presence or absence of necrosis, and have in common the recognition of three main categories of DCIS (ie, high, intermediate, and low grade).

  • High-grade lesions typically exhibit aneuploidy, lack estrogen and progesterone receptors, and have a high proliferative rate, overexpression of the human epidermal growth factor receptor 2 (HER2) oncogene, mutations of the p53 tumor suppressor gene with accumulation of its protein product, and angiogenesis in the surrounding stroma.
  • Low-grade lesions are typically diploid, estrogen- and progesterone receptor-positive, have a low proliferative rate, and rarely (if ever) show abnormalities of the HER2/neu or p53 oncogenes.
  • Lesions categorized histologically as intermediate grade are also intermediate between the high-grade and low-grade lesions with regard to the frequency of alterations in these biological markers.

These classification systems appear to correlate with biologic prognostic markers and predict groups of patients who are likely to have a recurrence of cancer following breast conservation therapy [15,18-30].

In 1997, a consensus conference was convened in an attempt to reach agreement on the classification of DCIS [31]. Although the panel did not endorse any single classification system, they recommended that certain features be routinely documented in the pathology report for DCIS lesions, including nuclear grade, the presence of necrosis, cell polarization, and architectural pattern(s).


Infiltrating ductal carcinoma is the most common type of invasive breast cancer, accounting for 70 to 80% of invasive lesions. It is also termed infiltrating carcinoma of no special type or infiltrating carcinoma not otherwise specified (NOS).

On gross pathologic evaluation, these lesions are typically hard, gray-white, gritty masses that invade the surrounding tissue in a haphazard fashion to create the characteristic irregular, stellate shape. They are characterized microscopically by cords and nests of tumor cells with varying amounts of gland formation, and cytologic features that range from bland to highly malignant. The malignant cells induce a fibrous response as they infiltrate the breast parenchyma, and this reaction is, in large part, responsible for the clinically and grossly palpable mass, the radiologic density, and solid sonographic characteristics of typical invasive carcinomas.

Infiltrating ductal carcinomas are divided into three grades based upon a combination of architectural and cytologic features, usually assessed utilizing a scoring system based on three parameters [32]:

  • Well-differentiated (grade 1) – Well-differentiated tumors have cells that infiltrate the stroma as solid nests of glands. The nuclei are relatively uniform with little or no evidence of mitotic activity (picture 4).
  • Moderately differentiated (grade 2) – Moderately differentiated tumors have cells that infiltrate as solid nests with some glandular differentiation. There is some nuclear pleomorphism and a moderate mitotic rate (picture 5).
  • Poorly differentiated (grade 3) – Poorly differentiated tumors are composed of solid nests of neoplastic cells without evidence of gland formation. There is marked nuclear atypia and considerable mitotic activity (picture 6).

A variable amount of associated ductal carcinoma in situ (DCIS) is present in most cases; the extent of DCIS but not lobular carcinoma in situ (LCIS) is an important prognostic factor in patients treated with breast conserving therapy in whom the surgical goal is complete excision of both intraductal and invasive carcinoma [33].


Infiltrating lobular carcinomas are the second most common type of invasive breast cancer, accounting for about 5 to 10% of invasive lesions.

Incidence rates of lobular cancer are rising faster than the rates of ductal carcinoma in the United States, and postmenopausal hormone therapy may be more strongly related to lobular cancer risk than to ductal cancer risk.

Some infiltrating lobular carcinomas have a macroscopic appearance identical to that of infiltrating ductal cancers. However, in many cases no mass lesion is grossly evident, and the excised breast tissue may have a normal or only slightly firm consistency. Thus, the microscopic size of invasive lobular carcinoma may be significantly greater than that measured grossly. Some pathologists have used lack of immunohistochemical staining for E-cadherin to distinguish invasive lobular carcinoma from invasive duct carcinoma. While it appears to be a reasonably accurate test, it is for the most part unnecessary in practice.

These tumors are characterized microscopically by small cells that insidiously infiltrate the mammary stroma and adipose tissue individually and in a single file pattern, often growing in a target-like configuration around normal breast ducts, frequently inducing only minimal fibrous reaction (picture 7). Associated lobular carcinoma in situ (LCIS) is present in approximately two-thirds of cases; however, ductal carcinoma in situ (DCIS) may also accompany invasive lobular carcinoma.

In addition to their different histologic appearance and mammographic characteristics, there are distinct prognostic and biologic differences between infiltrating lobular and ductal cancers:

  • Infiltrating lobular carcinomas have a higher frequency of bilaterality and multicentricity than infiltrating ductal carcinomas [34,35].
  • Infiltrating lobular carcinomas arise in older women and are larger and better differentiated tumors [34,36]. As a rule, invasive lobular carcinomas are estrogen receptor (ER)-positive, with variant lesions showing occasional variable expression.
  • While older series report a similar prognosis for infiltrating lobular cancers and invasive ductal lesions, subsequent reports suggest that outcomes (at least in the short-term) may be more favorable for lobular cancers and improving over time [37,38]. However, variants of infiltrating lobular carcinoma exist, some of which have a poorer prognosis [34].
  • As a group, invasive lobular carcinomas tend to metastasize later than invasive duct carcinomas and spread to unusual locations such as the peritoneum, meninges, and gastrointestinal tract [39].

There is an association between mutations in the cadherin (CDH1) gene and invasive lobular breast cancers. Lobular breast cancers have been observed to occur in 20 to 54% of women from families with hereditary diffuse gastric cancer who carry germline mutations in the CDH1 gene. However, germline CDH1 mutations can also be cosegregated with invasive lobular breast cancer in the absence of diffuse gastric cancer, suggesting that gastric cancer is not an obligatory hallmark of families with CDH1 mutations. Furthermore, more than half contain alterations in one of three key genes of the phosphatidylinositol 3-kinase pathway, PIK3CA, PTEN, and AKT1 [40], and approximately 50% of sporadic lobular breast cancers contain E-cadherin mutations [41,42].


A number of other histologic types account for the remaining invasive breast cancers. These include tubular carcinoma, mucinous carcinoma, medullary carcinoma, invasive micropapillary carcinoma, metaplastic carcinoma, adenoid cystic carcinoma, and others. Tumors of other histologies arising in the breast (lymphomas, sarcomas, phyllodes tumors) are discussed elsewhere.

Special clinical presentations of breast carcinomas, including Paget disease and inflammatory carcinoma, are discussed elsewhere.

Tubular carcinoma

Tubular carcinomas were relatively infrequent in the pre-mammography era, accounting for 2% or less of invasive breast cancers. However, in some series of mammographically screened populations the incidence is higher, accounting for 10 to 20% of invasive cancers.

Tubular carcinoma is characterized by the presence of well-formed tubular or glandular structures infiltrating the stroma (picture 8).

  • The tubules tend to be elongated, and many have pointed ends
  • The cells composing the tubules are cuboidal to columnar and often have apical cytoplasmic protrusions or «snouts»
  • The tumor cells are cytologically low grade
  • Associated ductal carcinoma in situ (DCIS), typically of the low-grade type, is present in about three-quarters of the cases

These lesions have a relatively favorable prognosis compared with infiltrating ductal carcinomas; the natural history is favorable, and metastases are rare [1,37,43-45].

Mucinous (colloid) carcinoma

Mucinous carcinomas account for between 1 and 2% of invasive breast cancers and appear to be more common in older patients. These lesions usually have a soft gelatinous appearance on gross examination, and they tend to be well circumscribed. Mucinous carcinomas are characterized microscopically by nests of tumor cells dispersed in large pools of extracellular mucus; the cells tend to have uniform, low-grade nuclei (picture 9). Similar to tubular carcinomas, these lesions also represent a prognostically favorable variant of invasive breast carcinoma [1,37,44,46].

Medullary carcinoma

Medullary carcinomas account for anywhere from 1 to 10% of invasive breast cancers. However, there is considerable interobserver variability in the diagnosis of this type of breast cancer which is, at least in part, dependent upon the classification system employed [47-49].

Medullary carcinomas are well circumscribed on macroscopic examination and are often soft and tan-brown with areas of hemorrhage or necrosis. Circumscription of the lesion is also evident microscopically. The tumor cells are poorly differentiated (high-grade), grow in a syncytial pattern, and have an intense associated lymphoplasmacytic infiltrate (picture 10), and this tumor is actually quite rare when strict diagnostic criteria are followed.

Medullary and medullary-like carcinomas occur more frequently in younger patients than other types of breast cancer. They are also more frequent in women who inherit mutations of the BRCA1 gene (10% of breast cancers are medullary in this population, as compared with <1% of non-BRCA1-related breast cancers). However, the majority of breast cancers in patients with BRCA1 gene mutations (90%) are not medullary [50].

The prognosis for pure medullary carcinomas appears to be somewhat more favorable than that of infiltrating ductal carcinomas, despite their aggressive histologic appearance [1,37,44,51,52]. For example, in a retrospective review of 12,409 patients with breast cancer, patients with medullary cancer (n = 127) had a significantly higher overall 14-year disease-free survival rate compared with patients with invasive ductal cancer (n = 8096) (76 versus 64%; hazard ratio [HR] 0.52, p = 0.0005) [52]. In addition, patients with medullary cancer also had a significantly higher overall survival rate (66 versus 57%; HR 0.75, p = 0.03).

Tubulolobular carcinoma

Tubulolobular carcinoma is an often unrecognized breast cancer variant that, as the name implies, has hybrid histologic characteristics of tubular and invasive lobular carcinoma with the same cells comprising well-formed glands contiguous with single-file infiltration of stroma. While immunohistochemical studies imply a ductal phenotype [53], from a radiologic and clinical point of view, the tumor is more akin to invasive lobular carcinoma in that its imaging characteristics are identical to lobular breast cancer, and there is the same tendency to multifocality and multicentricity. In terms of staging, however, the tumors behave more like invasive moderately differentiated ductal carcinoma in that they have the same likelihood of nodal metastases when matched by size. Often these tumors are misclassified as invasive carcinoma with mixed ductal and lobular features.

Micropapillary carcinoma

Invasive micropapillary carcinoma is a particularly aggressive form of cancer that has a proclivity for lymph node metastasis even when small in size [54].

Metaplastic carcinoma

Metaplastic carcinoma is a well circumscribed tumor that consists of various combinations of poorly differentiated ductal adenocarcinoma, mesenchymal (sarcomatous), and other epithelial (eg, squamous cell) components [55,56].

Whether these tumors have a worse prognosis than ordinary invasive ductal cancers is unclear. Some studies suggest that tumors in which the squamous cell component predominates (more than 90% of the malignant cells are of squamous type) are more aggressive and frequently treatment-refractory when compared with other infiltrating ductal cancers [57,58]. However, because metaplastic breast cancer was not officially recognized as a distinct pathologic diagnosis until 2000, knowledge about treatment patterns and outcomes is limited.

The characteristics of 892 metaplastic breast cancers reported to the National Cancer Database between 2001 and 2003 were compared with those of 255,164 typical infiltrating ductal carcinomas [56]. In contrast to patients with infiltrating ductal cancers, the following significant differences were noted in the group with metaplastic tumors:

  • Fewer T1 tumors (30 versus 65%)
  • More node-negative tumors (78 versus 66%)
  • More poorly differentiated or undifferentiated tumors (68 versus 39%)
  • Fewer estrogen receptor-positive tumors (11 versus 74%)

Treatment outcomes were not reported. Despite the perception of a worse prognosis, all metaplastic breast cancers are treated similarly to other invasive breast cancers [59-61].

Adenoid cystic carcinoma

The rare adenoid cystic carcinoma of the breast has a distinctive histologic pattern that is morphologically identical to adenoid cystic carcinoma found in the salivary glands (and other sites). This tumor tends to be associated with a favorable prognosis, even when tumor size is large; the reported incidence of axillary metastases in most series is less than 5% [62,63].

Histologic grading based upon the%age of solid areas (as is used for salivary gland tumors) has been suggested as being prognostically useful [64], although others disagree [63]. At least two series in which outcomes were not as favorable as in most reports were predominated by patients with higher-grade tumors (ie, the solid variant) [65,66].


  • Ductal carcinoma in situ (DCIS) is characterized by a proliferation of abnormal cells confined within the mammary ductal system.
    • DCIS is commonly classified according to architectural and cytologic features and cell necrosis as low and intermediate grade (papillary, cribriform, and solid) and high grade (comedo).
    • DCIS represents a precursor to invasive breast cancer.
  • The invasive breast carcinomas consist of several histologic subtypes.
    • Infiltrating ductal carcinoma is the most common type of invasive breast cancer, accounting for 70 to 80% of invasive cancers.
    • Infiltrating lobular carcinoma is the second most common invasive breast cancer, accounting for 5 to 10% of invasive cancers.
    • As compared with infiltrating ductal carcinomas, infiltrating lobular carcinomas tend to be multicentric and/or bilateral, more differentiated, hormone receptor-positive, arise in older women, metastasize later, and spread to unusual locations, such as the meninges, peritoneum, or gastrointestinal tract.
    • Other less common invasive breast carcinoma histologies include tubular, mucinous, and medullary carcinomas.


  1. Li CI, Uribe DJ, Daling JR. Clinical characteristics of different histologic types of breast cancer. Br J Cancer 2005; 93:1046.
  2. Dillon DA, Guidi AJ, Schnitt SJ. Pathology of invasive breast cancer. In: Diseases of the Breast, 4th, Harris JR, Lippman ME, Morrow M, Osborne CK (Eds), Lippincott, Williams and Wilkins, Philadelphia 2009. p.386.
  3. Allred DC. Ductal carcinoma in situ: terminology, classification, and natural history. J Natl Cancer Inst Monogr 2010; 2010:134.
  4. Azzopardi JG. Problems in Breast Pathology, WB Saunders, Philadelphia 1963. p.244.
  5. Page DL, Anderson TJ. Diagnostic Histopathology of the Breast, Churchill Livingstone, Edinburgh 1987. p.157.
  6. Rosen PP, Oberman H. Tumors of the Mammary Gland, Armed Forces Institute of Pathology, Washington, DC 1993. p.143.
  7. Alfred C. Ductal carcinoma in situ. In: Diseases of the Breast, 4th, Harris JR, Lippman ME, Morrow M, Osborne CK (Eds), Lippincott-Raven, Philadelphia 2009. p.321.
  8. Schwartz GF, Patchefsky AS, Finklestein SD, et al. Nonpalpable in situ ductal carcinoma of the breast. Predictors of multicentricity and microinvasion and implications for treatment. Arch Surg 1989; 124:29.
  9. Silverstein MJ, Waisman JR, Gamagami P, et al. Intraductal carcinoma of the breast (208 cases). Clinical factors influencing treatment choice. Cancer 1990; 66:102.
  10. Fisher ER, Dignam J, Tan-Chiu E, et al. Pathologic findings from the National Surgical Adjuvant Breast Project (NSABP) eight-year update of Protocol B-17: intraductal carcinoma. Cancer 1999; 86:429.
  11. Grabowski J, Salzstein SL, Sadler GR, Blair S. Intracystic papillary carcinoma: a review of 917 cases. Cancer 2008; 113:916.
  12. Eusebi V, Foschini MP, Cook MG, et al. Long-term follow-up of in situ carcinoma of the breast with special emphasis on clinging carcinoma. Semin Diagn Pathol 1989; 6:165.
  13. Fisher ER, Brown R. Intraductal signet ring carcinoma. A hitherto undescribed form of intraductal carcinoma of the breast. Cancer 1985; 55:2533.
  14. Rosen PP, Scott M. Cystic hypersecretory duct carcinoma of the breast. Am J Surg Pathol 1984; 8:31.
  15. Lagios MD, Margolin FR, Westdahl PR, Rose MR. Mammographically detected duct carcinoma in situ. Frequency of local recurrence following tylectomy and prognostic effect of nuclear grade on local recurrence. Cancer 1989; 63:618.
  16. Poller DN, Silverstein MJ, Galea M, et al. Ideas in pathology. Ductal carcinoma in situ of the breast: a proposal for a new simplified histological classification association between cellular proliferation and c-erbB-2 protein expression. Mod Pathol 1994; 7:257.
  17. Holland R, Peterse JL, Millis RR, et al. Ductal carcinoma in situ: a proposal for a new classification. Semin Diagn Pathol 1994; 11:167.
  18. Pinder SE, Duggan C, Ellis IO, et al. A new pathological system for grading DCIS with improved prediction of local recurrence: results from the UKCCCR/ANZ DCIS trial. Br J Cancer 2010; 103:94.
  19. Bur ME, Zimarowski MJ, Schnitt SJ, et al. Estrogen receptor immunohistochemistry in carcinoma in situ of the breast. Cancer 1992; 69:1174.
  20. Meyer JS. Cell kinetics of histologic variants of in situ breast carcinoma. Breast Cancer Res Treat 1986; 7:171.
  21. Killeen JL, Namiki H. DNA analysis of ductal carcinoma in situ of the breast. A comparison with histologic features. Cancer 1991; 68:2602.
  22. van de Vijver MJ, Peterse JL, Mooi WJ, et al. Neu-protein overexpression in breast cancer. Association with comedo-type ductal carcinoma in situ and limited prognostic value in stage II breast cancer. N Engl J Med 1988; 319:1239.
  23. Bartkova J, Barnes DM, Millis RR, Gullick WJ. Immunohistochemical demonstration of c-erbB-2 protein in mammary ductal carcinoma in situ. Hum Pathol 1990; 21:1164.
  24. Lodato RF, Maguire HC Jr, Greene MI, et al. Immunohistochemical evaluation of c-erbB-2 oncogene expression in ductal carcinoma in situ and atypical ductal hyperplasia of the breast. Mod Pathol 1990; 3:449.
  25. Poller DN, Roberts EC, Bell JA, et al. p53 protein expression in mammary ductal carcinoma in situ: relationship to immunohistochemical expression of estrogen receptor and c-erbB-2 protein. Hum Pathol 1993; 24:463.
  26. O’Malley FP, Vnencak-Jones CL, Dupont WD, et al. p53 mutations are confined to the comedo type ductal carcinoma in situ of the breast. Immunohistochemical and sequencing data. Lab Invest 1994; 71:67.
  27. Guidi AJ, Fischer L, Harris JR, Schnitt SJ. Microvessel density and distribution in ductal carcinoma in situ of the breast. J Natl Cancer Inst 1994; 86:614.
  28. Bobrow LG, Happerfield LC, Gregory WM, et al. The classification of ductal carcinoma in situ and its association with biological markers. Semin Diagn Pathol 1994; 11:199.
  29. Zafrani B, Leroyer A, Fourquet A, et al. Mammographically-detected ductal in situ carcinoma of the breast analyzed with a new classification. A study of 127 cases: correlation with estrogen and progesterone receptors, p53 and c-erbB-2 proteins, and proliferative activity. Semin Diagn Pathol 1994; 11:208.
  30. Wärnberg F, Nordgren H, Bergh J, Holmberg L. Ductal carcinoma in situ of the breast from a population-defined cohort: an evaluation of new histopathological classification systems. Eur J Cancer 1999; 35:714.
  31. Consensus Conference on the classification of ductal carcinoma in situ. The Consensus Conference Committee. Cancer 1997; 80:1798.
  32. Elston CW, Ellis IO. Pathological prognostic factors in breast cancer. I. The value of histological grade in breast cancer: experience from a large study with long-term follow-up. Histopathology 2002; 41:154.
  33. Abner AL, Connolly JL, Recht A, et al. The relation between the presence and extent of lobular carcinoma in situ and the risk of local recurrence for patients with infiltrating carcinoma of the breast treated with conservative surgery and radiation therapy. Cancer 2000; 88:1072.
  34. Orvieto E, Maiorano E, Bottiglieri L, et al. Clinicopathologic characteristics of invasive lobular carcinoma of the breast: results of an analysis of 530 cases from a single institution. Cancer 2008; 113:1511.
  35. Winchester DJ, Chang HR, Graves TA, et al. A comparative analysis of lobular and ductal carcinoma of the breast: presentation, treatment, and outcomes. J Am Coll Surg 1998; 186:416.
  36. Pestalozzi BC, Zahrieh D, Mallon E, et al. Distinct clinical and prognostic features of infiltrating lobular carcinoma of the breast: combined results of 15 International Breast Cancer Study Group clinical trials. J Clin Oncol 2008; 26:3006.
  37. Li CI, Moe RE, Daling JR. Risk of mortality by histologic type of breast cancer among women aged 50 to 79 years. Arch Intern Med 2003; 163:2149.
  38. Cristofanilli M, Gonzalez-Angulo A, Sneige N, et al. Invasive lobular carcinoma classic type: response to primary chemotherapy and survival outcomes. J Clin Oncol 2005; 23:41.
  39. Ferlicot S, Vincent-Salomon A, Médioni J, et al. Wide metastatic spreading in infiltrating lobular carcinoma of the breast. Eur J Cancer 2004; 40:336.
  40. Desmedt C, Zoppoli G, Gundem G, et al. Genomic Characterization of Primary Invasive Lobular Breast Cancer. J Clin Oncol 2016; 34:1872.
  41. Berx G, Cleton-Jansen AM, 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; 13:1919.
  42. De Leeuw WJ, Berx G, Vos CB, et al. Simultaneous loss of E-cadherin and catenins in invasive lobular breast cancer and lobular carcinoma in situ. J Pathol 1997; 183:404.
  43. Liu GF, Yang Q, Haffty BG, Moran MS. Clinical-pathologic features and long-term outcomes of tubular carcinoma of the breast compared with invasive ductal carcinoma treated with breast conservation therapy. Int J Radiat Oncol Biol Phys 2009; 75:1304.
  44. Thurman SA, Schnitt SJ, Connolly JL, et al. Outcome after breast-conserving therapy for patients with stage I or II mucinous, medullary, or tubular breast carcinoma. Int J Radiat Oncol Biol Phys 2004; 59:152.
  45. Sullivan T, Raad RA, Goldberg S, et al. Tubular carcinoma of the breast: a retrospective analysis and review of the literature. Breast Cancer Res Treat 2005; 93:199.
  46. Di Saverio S, Gutierrez J, Avisar E. A retrospective review with long term follow up of 11,400 cases of pure mucinous breast carcinoma. Breast Cancer Res Treat 2008; 111:541.
  47. Gaffey MJ, Mills SE, Frierson HF Jr, et al. Medullary carcinoma of the breast: interobserver variability in histopathologic diagnosis. Mod Pathol 1995; 8:31.
  48. Ridolfi RL, Rosen PP, Port A, et al. Medullary carcinoma of the breast: a clinicopathologic study with 10 year follow-up. Cancer 1977; 40:1365.
  49. Wargotz ES, Silverberg SG. Medullary carcinoma of the breast: a clinicopathologic study with appraisal of current diagnostic criteria. Hum Pathol 1988; 19:1340.
  50. Armes JE, Venter DJ. The pathology of inherited breast cancer. Pathology 2002; 34:309.
  51. Vu-Nishino H, Tavassoli FA, Ahrens WA, Haffty BG. Clinicopathologic features and long-term outcome of patients with medullary breast carcinoma managed with breast-conserving therapy (BCT). Int J Radiat Oncol Biol Phys 2005; 62:1040.
  52. Huober J, Gelber S, Goldhirsch A, et al. Prognosis of medullary breast cancer: analysis of 13 International Breast Cancer Study Group (IBCSG) trials. Ann Oncol 2012; 23:2843.
  53. Esposito NN, Chivukula M, Dabbs DJ. The ductal phenotypic expression of the E-cadherin/catenin complex in tubulolobular carcinoma of the breast: an immunohistochemical and clinicopathologic study. Mod Pathol 2007; 20:130.
  54. Walsh MM, Bleiweiss IJ. Invasive micropapillary carcinoma of the breast: eighty cases of an underrecognized entity. Hum Pathol 2001; 32:583.
  55. Tavassoli FA. Classification of metaplastic carcinomas of the breast. Pathol Annu 1992; 27 Pt 2:89.
  56. Pezzi CM, Patel-Parekh L, Cole K, et al. Characteristics and treatment of metaplastic breast cancer: analysis of 892 cases from the National Cancer Data Base. Ann Surg Oncol 2007; 14:166.
  57. Hennessy BT, Krishnamurthy S, Giordano S, et al. Squamous cell carcinoma of the breast. J Clin Oncol 2005; 23:7827.
  58. Behranwala KA, Nasiri N, Abdullah N, et al. Squamous cell carcinoma of the breast: clinico-pathologic implications and outcome. Eur J Surg Oncol 2003; 29:386.
  59. Dave G, Cosmatos H, Do T, et al. Metaplastic carcinoma of the breast: a retrospective review. Int J Radiat Oncol Biol Phys 2006; 64:771.
  60. Rayson D, Adjei AA, Suman VJ, et al. Metaplastic breast cancer: prognosis and response to systemic therapy. Ann Oncol 1999; 10:413.
  61. Chao TC, Wang CS, Chen SC, Chen MF. Metaplastic carcinomas of the breast. J Surg Oncol 1999; 71:220.
  62. Vranic S, Bender R, Palazzo J, Gatalica Z. A review of adenoid cystic carcinoma of the breast with emphasis on its molecular and genetic characteristics. Hum Pathol 2013; 44:301.
  63. Kleer CG, Oberman HA. Adenoid cystic carcinoma of the breast: value of histologic grading and proliferative activity. Am J Surg Pathol 1998; 22:569.
  64. Ro JY, Silva EG, Gallager HS. Adenoid cystic carcinoma of the breast. Hum Pathol 1987; 18:1276.
  65. Millar BA, Kerba M, Youngson B, et al. The potential role of breast conservation surgery and adjuvant breast radiation for adenoid cystic carcinoma of the breast. Breast Cancer Res Treat 2004; 87:225.
  66. Shin SJ, Rosen PP. Solid variant of mammary adenoid cystic carcinoma with basaloid features: a study of nine cases. Am J Surg Pathol 2002; 26:413.

WordPress: 66.96MB | MySQL:104 | 1,265sec