Familial gastrointestinal stromal tumors associated with dysphagia and novel type germline mutation of KIT gene☆☆☆

Abstract 

A family with multiple gastrointestinal stromal tumors (GISTs), a new type of germline mutation of KIT gene, and dysphagia is reported. The mutation was observed at Asp-820 in tyrosine kinase (TK) II domain. Mutations in TK II domain have been found in mast cell and germ cell tumors but not in GISTs, and the present family members are the first reported cases of GISTs with TK II domain mutations, including sporadic GISTs. Because interleukin 3–dependent Ba/F3 murine lymphoid cells transfected with the mutant KIT complementary DNA grew autonomously without any growth factors and formed tumors in nude mice, the mutation was considered to be gain-of-function type. Family members with the germline KIT mutation reported dysphagia, but those without the mutation did not. The mechanism of dysphagia was examined with gastrointestinal fiberscopy, endoscopic ultrasonography, and esophageal manometry. No mechanical obstruction was found, and the esophagus was not remarkably dilated. In the family members with dysphagia, endoscopic ultrasonography at the esophagocardiac junction showed a thickened hyperechoic layer between the circular and longitudinal muscle layers, suggesting hyperplasia of interstitial cells of Cajal at the myenteric plexus layer. Manometry showed low resting lower esophageal sphincter pressure and abnormal simultaneous contractions of the esophagus without normal peristalsis. These findings indicate that the dysphagia of the present family is different from typical achalasia. This is the first report of familial dysphagia caused by germline gain-of-function mutation of the KIT gene at the TK II domain.

GASTROENTEROLOGY 2002;122:1493-1499

Abbreviations:  CT , computed tomography, EUS , endoscopic ultrasonography, GIST , gastrointestinal stromal tumor, ICC , interstitial cells of Cajal, IL , interleukin, KIT , c-kit receptor tyrosine kinase, MTT , 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, rm , recombinant mouse, SCF , stem cell factor, TK , tyrosine kinase