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Primary intestinal-type adenocarcinoma of the buccal mucosa: A case report and literature review.
Kikuchi, Kentaro; Fukunaga, Shuichi; Ide, Fumio; Hoshino, Miyako; Inoue, Harumi; Miyazaki, Yuji; Li, Tie-Jun; Kusama, Kaoru.
Afiliação
  • Kikuchi K; Division of Pathology, Department of Diagnostic and Therapeutic Sciences, Meikai University School of Dentistry, Saitama, Japan; Department of Oral Pathology, Peking University School of Stomatology, Beijing, China. Electronic address: k-kikuchi@dent.meikai.ac.jp.
  • Fukunaga S; Department of dental and oral surgery, Hanyu General Hospital, Saitama, Japan.
  • Ide F; Division of Pathology, Department of Diagnostic and Therapeutic Sciences, Meikai University School of Dentistry, Saitama, Japan.
  • Hoshino M; Division of Pathology, Department of Diagnostic and Therapeutic Sciences, Meikai University School of Dentistry, Saitama, Japan.
  • Inoue H; Division of Pathology, Department of Diagnostic and Therapeutic Sciences, Meikai University School of Dentistry, Saitama, Japan.
  • Miyazaki Y; Division of Basic Biology, Department of Oral Biology and Tissue Engineering, Meikai University School of Dentistry, Saitama, Japan.
  • Li TJ; Department of Oral Pathology, Peking University School of Stomatology, Beijing, China.
  • Kusama K; Division of Pathology, Department of Diagnostic and Therapeutic Sciences, Meikai University School of Dentistry, Saitama, Japan.
Article em En | MEDLINE | ID: mdl-29941401
ABSTRACT
Intestinal-type adenocarcinoma of the primary salivary glands is extremely rare. So far, only 11 cases of primary intestinal-type adenocarcinoma of the oral cavity and major salivary glands have been reported. Two of those tumors arose in the floor of mouth, 7 in the tongue, and 2 in the major salivary glands. However, it has remained unclear whether these tumors are derived from mature salivary glands, and primary intestinal-type adenocarcinoma of the buccal mucosa has not been reported previously. Here, we present the first documented case of primary intestinal-type adenocarcinoma arising in a minor salivary gland of the buccal mucosa. Histopathologically, the tumor resembled a well-differentiated or mucinous colonic adenocarcinoma. Immunohistochemically, the tumor cells were diffusely positive for AE1/AE3, CAM5.2, CK7, SATB2, ß-catenin, p53, Ki-67, MUC2, and MUC5 AC. CK14 and CK20 were positive in some of the tumor cells. CDX2, CA19-9, SP-A, TTF-1, PSA, SMA, p63, and cyclin D1 were negative in the tumor cells. The tumor in the present case may have originated from salivary gland duct epithelium that underwent transformation to phenotypic intestinal-type epithelium. In this very rare case of primary intestinal-type adenocarcinoma of the buccal mucosa, we considered diagnostic markers that could be indicative of mature salivary gland origin.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Adenocarcinoma / Adenocarcinoma Mucinoso / Proteínas de Ligação à Região de Interação com a Matriz Tipo de estudo: Systematic_reviews Limite: Humans Idioma: En Revista: Oral Surg Oral Med Oral Pathol Oral Radiol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Adenocarcinoma / Adenocarcinoma Mucinoso / Proteínas de Ligação à Região de Interação com a Matriz Tipo de estudo: Systematic_reviews Limite: Humans Idioma: En Revista: Oral Surg Oral Med Oral Pathol Oral Radiol Ano de publicação: 2019 Tipo de documento: Article