Colorectal
adenosquamous carcinoma (ASC) is exceedingly rare, comprising less than 0.1% of all colorectal
malignancies, and is characterized by the admixture of glandular and squamous components. Due to its rarity, immunohistochemical and biological profiles have not been well investigated. The clinico-pathologic features of 29 cases of primary colorectal
adenosquamous carcinomas, including four synchronous
metastases, as well as the immunohistochemical expression of
keratin 20, CDX2,
keratin 34βE12,
keratin 5/6, p63, p40, β-
Catenin,
Cyclin D1 and mismatch repair
protein (MMR) expression in both squamous and glandular components are described. All ASCs showed aggressive clinico-pathologic features; all cases showed at least one aggressive pathologic characteristic (poorly differentiated, vascular invasion, infiltrative growth pattern) and 69% of cases were either stage III or IV. The squamous component was
keratin 34βE12 positive in all cases and
keratin 5/6 positive in 27 cases, while only 7 cases showed p63 and/or p40 expression. β-
Catenin and
Cyclin D1 showed different expression, with nuclear staining of
Cyclin D1 in the squamous component of all cases (both primary and metastatic lesions) and nuclear staining of β-
Catenin predominantly in the glandular component. All but one case showed proficient MMR profile. Sixteen patients (64%) died of their disease with median survival of 10 months. ASC show aggressive clinical outcome and aggressive pathologic characteristics. A peculiar
keratin 34βE12 positive profile in the squamous component is seen differing from
squamous cell carcinoma and non-intestinal ASC. The staining patterns for β-
Catenin and
Cyclin D1 between components, supports a possible divergent clonal evolution of the
neoplasm.