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Gastric‐type endocervical glandular neoplasms associated with aberrant p16 expression and K‐RAS gene mutation in Peutz‐Jeghers syndrome
Authors:Shigemi Ito  Toru Tase  Kennichi Satoh  Miyuki Ueki  Ikuro Sato  Hironobu Sasano
Affiliation:1. Department of Pathology, Miyagi Cancer Center, , Natori, Japan;2. Department of Gynecology, Miyagi Cancer Center, , Natori, Japan;3. Division of Cancer Stem Cell, Miyagi Cancer Research Institute, , Natori, Japan;4. Department of Pathology, Tohoku University School of Medicine, , Sendai, Japan
Abstract:In this report, unique endocervical glandular lesions exhibiting gastric differentiation were examined in a patient with Peutz‐Jeghers syndrome. The result of the human papillomavirus (HPV) in situ hybridization (ISH) for the hysterectomy specimens was negative, but they demonstrated a papillary mucinous adenocarcinoma at the proximal endocervix continuous to atypical lobular endocervical glandular hyperplasia. Both contained MUC6‐positive neutral mucin in cytoplasm, and showed different immunoreactivity to p16, Ki‐67, and p53. Moreover, they harbored the identical K‐RAS gene mutation suggesting that there was a common origin. Somatic K‐RAS mutation and defective function of p16 may have been involved in the tumorigenesis of these unusual mucinous neoplasms.
Keywords:cervical adenocarcinoma  K‐RAS  lobular endocervical glandular hyperplasia  p16  Peutz‐Jeghers syndrome
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