| Literature DB >> 25120845 |
Yan-Fang Liang1, Bin Kong2, Wen-Yu Xiang2, Jian-Bo Ruan1, Ling-Mei Wang1, Can Chen1, Wei-Hua Xu3, Qiu-Liang Wu4, Jin-Cheng Zeng2, Jun-Fa Xu2.
Abstract
ACC derived from nasopharyngeal epithelial cells is rare, usually benign. In this article, we reported a nasopharyngeal adenoid cystic carcinoma (NACC) in a 31-year-old woman with a symptom of hoarseness, headache, epistaxis slightly, diplopia, facial numbness and dysphagia near 3 months. A tumor on the right side of the nasopharynx was confirmed by laryngoscope check and MRI of the skull base. Histopathological findings showed that tumor cells were arranged in cord-like or acinar-like by atypical hyperplastic epithelial cells forming a cribriform and tubular pattern, and immunohistochemical findings showed that tumor tissues were immunopositive for p63 (+), CK7 (+), CK19 (+), CK8 (+), CK18 (+), SMA (+), CK (+), p53 (++), S-100 (+) and Ki-67 (5%+), and negative for CD34 (-), CK5/6 (-), CEA (-) and CD117 (-). Patient was treated by surgical operation and radiotherapy, and was followed-up near 10 months, no local recurrence and distant metastasis.Entities:
Keywords: Adenoid cystic carcinoma; immunohistochemistry; nasopharynx
Mesh:
Substances:
Year: 2014 PMID: 25120845 PMCID: PMC4129080
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625