Unusually early presentation of small-bowel adenocarcinoma in a patient with Peutz-Jeghers syndrome. | Read by QxMD (original) (raw)

Case Reports

Journal Article

Research Support, N.I.H., Extramural

Michael F Wangler, Rishikesh Chavan, M John Hicks, Jed G Nuchtern, Madhuri Hegde, Sharon E Plon, Patrick A Thompson

Peutz-Jeghers syndrome (PJS) is an autosomal dominant cancer predisposition syndrome characterized by melanotic macules and hamartomatous polyps. Small-bowel surveillance in the pediatric PJS population is not designed to identify small-bowel malignancy, which is thought to arise in adulthood. A 13-year-old boy presented with lead-point intussusception, requiring emergent surgical resection. A mucinous adenocarcinoma was found arising from high-grade dysplasia within a polyp. On the basis of these findings and mucosal pigmentation, he was diagnosed with PJS. DNA sequencing revealed a heterozygous c.921-1G>T STK11 mutation. This case is the earliest onset of small-bowel carcinoma in PJS, an observation relevant to surveillance guidelines.

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