Bile duct adenocarcinoma with minor micropapillary component: a case report
© Kondo; licensee BioMed Central Ltd. 2009
Received: 09 January 2009
Accepted: 14 January 2009
Published: 14 January 2009
Invasive micropapillary carcinoma (IMPC) is defined as a carcinoma composed of small clusters of tumor cells lying within clear spaces which simulate lymphovascular channels. This histologic pattern has been described in various organs, including the breast, lung, urinary bladder, ovary, stomach, pancreas, and major salivary glands. Although rarely observed as a pure histologic component, IMPC is usually mixed with conventional carcinoma, and is therefore often referred to as carcinoma with a micropapillary component. IMPCs are invariably associated with a high degree of aggressiveness, extensive lymphovascular invasion, extensive lymph node metastases, and poor prognosis. Here a case of bile duct adenocarcinoma with minor micropapillary component is described.
Invasive micropapillary carcinoma (IMPC) is defined as a carcinoma composed of small clusters of tumor cells lying within clear spaces, and was proposed as a histological variant of invasive breast carcinoma with poor clinical prognosis . This distinct histologic pattern has been described in various organs, including the urinary bladder, lung, ovary, colon, stomach, pancreas, and major salivary glands [2–9]. IMPC is usually mixed with otherwise conventional carcinoma , and is therefore often referred to as carcinoma with a micropapillary component. IMPCs are all invariably associated with a high degree of aggressiveness, extensive lymphovascular invasion, extensive lymph node metastases, and poor prognosis .
IMPC has distinctive histologic features characterized by tufts of tumor cells arranged in pseudopapillary patterns without fibrovascular cores and surrounded by empty and clear spaces. This "inside-out growth" structure has been attributed to the rotation of cell polarization, whereby the stroma-facing (basal) surface of the cells acquires "apical" properties . This inversion of cell polarity has been disclosed immunohistochemically by the outer membranous staining pattern of EMA only toward the stroma . Compared with conventional carcinomas of similar size, hypothetically this reverse polarization in IMPC facilitates the secretion by tumor cells of molecules, such as metalloproteinases, known to be responsible for stromal and vascular invasion, permitting easier dissemination and a higher tendency for lymph node metastases .
All pancreatic micropapillary carcinoma reported arose from the ampullo-pancreatobiliary region (pancreatic head). Occurrence of the micropapillary component in the adenocarcinoma of gastrointestinal tract may be attributable to the continuous exposure of the mucosa to bile acids . Taken together, it is suggested that the effect of bile juice especially the reflux may be important as an etiological factor of the micropapillary carcinoma in this region (around pancreatic head).
On the other hand, invasive micropapillary carcinoma of the ampullo-pancreatobiliary region is often associated with tumor-infiltrating neutrophils . In this case, numerous neutrophils were found around conventional adenocarcinoma (Fig. 2A) and there was mild eosinophilic infiltration around micropapillary component (not shown). The phenomenon (neutrophilic infiltration) was not reported in micropapillary carcinomas of other organs other than pancreas , and unexplained factors, such as chemotactic factors, may be responsible.
This case is bile duct cancer with small foci (2 mm in size) of micropapillary component. No reports have described the prognosis of cancer with such a small portion of micropapillary carcinoma. Because the presence of the minor micropapillary component may be ignored, carcinomas with a minor micropapillary component need to be carefully analyzed or followed up to understand their pathologic and prognostic characters.
In summary, the first case of bile duct cancer with minor micropapillary component metastasizing to the regional lymph node as a micrometastasis is reported.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
I thank Nao Sakumoto-Yoshida, Mika Ohya, and Yuko Nishikawa at Shinko Hospital for their excellent technical assistance.
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