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

研究成果: Article

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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.

元の言語English
ページ(範囲)884-888
ページ数5
ジャーナルHuman Pathology
45
発行部数4
DOI
出版物ステータスPublished - 2014 4

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ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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