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Journal of Clinical Pathology logoLink to Journal of Clinical Pathology
letter
. 2007 Aug;60(8):958–959. doi: 10.1136/jcp.2007.047191

CD10 positivity in breast epithelial neoplasms

Amanpreet S Bains 1, Jagmohan S Sidhu 1
PMCID: PMC1994501  PMID: 17660345

We read with great interest the study of Kalof et al1 concerning immunostaining patterns of myoepithelial cells in breast lesions. The authors identified focal CD10 staining of breast epithelial cells. We recently saw a case of co‐existent intraductal papilloma, intraductal carcinoma and infiltrating ductal carcinoma of breast (figs 1 and 2). The cytoplasm of epithelial cells in all components was pan‐cytokeratin positive and CD10 positive (figs 3 and 4) in addition to myoepithelial CD10 staining in the intraductal papilloma. Kalof et al also mentioned the study of Moritani et al,2 which showed lack of CD10 positivity in both non‐neoplastic and neoplastic breast epithelia. Methodological differences were mentioned by Kalof et al as possible reason(s) for the discrepant results between their study and that of Moritani et al. Comparison of the methods used in the study of Kalof et al, that of Moritani et al and our case study (table 1) indicates that CD10 immunostaining methods using 56C6 clone and/or non‐heat antigen retrieval detect CD10 expression in non‐neoplastic and neoplastic breast epithelial cells.

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Figure 1 H and E stain (×200) showing a papilloma.

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Figure 2 H and E stain (×200) showing an invasive ductal carcinoma.

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Figure 3 CDI0 immunostain (×400). Left: epithelial cytoplasmic positivity in papilloma; right: cytoplasmic positivity in invasive ductal carcinoma.

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Figure 4 CD10 immunostain (×1000) showing epithelial cytoplasmic staining.

Table 1 Comparison of CD10 immunohistochemical methods.

Method Kalof et al Moritani et al Our study
Antigen retrieval Sodium citrate, pH 6.0 (Dako, Autoclaving at 121°C for 25 min CCI (Tris/borate/EDTA), pH 8 (Ventana
Carpentaria, CA, USA) Medical Systems, Tucson, AZ, USA)
Antibody clone Monoclonal, clone 56C6 (NCL‐CD10‐270; NU‐N1(Japanese Nichirei, Tokyo, Monoclonal, clone 56C6 (Cell Marque,
NovoCastra, Newcastle upon Tyne, UK) Japan) Hot Springs, AZ, USA)
Antibody dilution 1:80 1:50 Prediluted (dilution unknown)
Signal detection Avidin‐biotin‐peroxidase method Streptavidin‐biotin‐peroxidase Streptavidin‐biotin‐peroxidase method
with diamino‐ benzidine (DAB) method with DAB with DAB

In their in vitro study of phenotypic and functional characterisation of a multipotent epithelial cell in the normal adult human breast, Stingl et al3 identified a bipotent human breast epithelial cell progenitor that can express MUC‐1, CD10 and epithelial‐specific antigen and can generate mixed colonies of both epithelial and myoepithelial cells. Therefore, it is possible to see CD10 expression in the breast luminal epithelial cells arising from these bipotent cells.

Although we cannot draw any conclusions about CD10 expression in breast epithelium based on the study by Kalof et al and our single case result, CD10 positivity in epithelial cells should not rule out the possibility of primary breast cancer during the work‐up of a metastatic adenocarcinoma. Larger studies using different CD10 antibody clones and different antigen retrieval methods could help clarify CD10 positivity in mammary epithelium.

Footnotes

Competing interests: None declared.

References

  • 1.Kalof A N, Tam D, Beatty B.et al Immunostaining patterns of myoepithelial cells in breast lesions: a comparison of CD10 and smooth muscle myosin heavy chain. J Clin Pathol 200457625–629. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Moritani S, Kushima R, Sugihara H.et al Availability of CD10 immunohistochemistry as a marker of breast myoepithelial cells on paraffin sections. Mod Pathol 200215397–405. [DOI] [PubMed] [Google Scholar]
  • 3.Stingl J, Eaves C J, Kuusk U.et al Phenotypic and functional characterization in vitro of a multipotent epithelial cell present in the normal adult human breast. Differentiation 199863201–213. [DOI] [PubMed] [Google Scholar]

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