| Literature DB >> 31912868 |
Lei Zhang1, Xiaofeng Huang1, Ting Zhou1, Hongbao Cao2.
Abstract
Microcystic adnexal carcinoma (MAC) is a rare, locally aggressive malignant neoplasm that derives from cutaneous eccrine/apocrine glands. MAC is classified as an eccrine/apocrine gland tumor and usually occurs in the skin. Here, we characterized and compared two cases of MAC. One is extremely rare in terms of its occurrence in the tongue. The other occurred in the lip, which is common. Histories of disease, diagnosis, and differentials were reviewed by attending physicians. Hematoxylin and eosin (HE) slides were evaluated by an experienced pathologist. Immunological markers for malignant eccrine/apocrine gland tumors were used to characterize the tumor's nature. The examined markers included EMA, CK5/6, CK8/18, CK7, CK20, p63, S-100, Calponin, CD10, MYB, Bcl-2, Her-2, CD34, SMA, p53, CD43, CD117, and Ki-67. Both patients were males, presenting with painless lumps in the lower lip and in the tongue, respectively. Both lumps were similar in terms of appearance, being whitish and infiltrative with irregular borders. Both tumors also had similar histological features with nests of bland keratinocytes, cords and ductal differentiation filled with Periodic Acid-Schiff (PAS) positive eosinophilic material. In both cases, circular or ovary tumor cells invaded into muscles and nerves. All tumor cells wereCK5/6, CK8/18, EMA, and CK7 positive. Particularly, keratinocytes were p63 positive, and paraductal cells were p63, S-100 and SMA positive. Therefore, the rare case of MAC in the tongue appears to derive from the salivary gland. Copyright 2020 The Author(s).Entities:
Keywords: Histopathology; Immunology; Microcystic adnexal carcinoma; differential diagnosis; salivary gland
Year: 2020 PMID: 31912868 DOI: 10.1042/BSR20191557
Source DB: PubMed Journal: Biosci Rep ISSN: 0144-8463 Impact factor: 3.840