Multiple gastrointestinal stromal tumors with novel germline c-kit gene mutation, K642T, at exon 13

Kazuhiro Yamanoi, Kayoko Higuchi, Hirofumi Kishimoto, Yasunori Nishida, Masato Nakamura, Motohiro Sudoh, Seiichi Hirota

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Multiple gastrointestinal stromal tumors (GISTs) caused by germline c-kit gene mutations are an extremely rare autosomal dominant disorder. A 57-year-old Japanese woman was referred to a hospital for appetite loss and severe weight loss. She had 2 large abdominal masses around the stomach, which were surgically resected. Histological examination revealed that these tumors were GISTs. Multiple microscopic GISTs and diffuse hyperplasia of the interstitial cells of Cajal were also seen in the background gastric and small intestinal walls. Characteristically, the GISTs showed severe hyalinization with calcification and partial heterotopic ossification, which may have caused the patient's severe dysphagia. Mutational analysis of the c-kit gene revealed a substitution at codon 642 in exon 13 (K642T) in the tumor, normal ileal mucosa and peripheral blood leukocytes, indicating that the mutation is in the germline. This is the first case of multiple GISTs with novel germline c-kit gene mutation at exon 13.

Original languageEnglish
Pages (from-to)884-888
Number of pages5
JournalHuman Pathology
Volume45
Issue number4
DOIs
Publication statusPublished - 2014 Apr

Keywords

  • Exon 13
  • Familial
  • GIST
  • Germline mutation
  • Heterotopic ossification

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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