Peutz-Jeghers syndrome and family survey: a case report.

TitlePeutz-Jeghers syndrome and family survey: a case report.
Publication TypeJournal Article
Year of Publication2013
AuthorsLi Y, Zeng Q, Liao Z, Zhang G, Xiao R, Wen H
JournalInternational journal of clinical and experimental pathology
Volume6
Issue5
Pagination982-4
Date Published2013
Abstract

Peutz-Jeghers syndrome (PJS) is a rare inherited autosomal dominant disease characterized by mucocutaneous pigmentation and multiple polyps in the gastrointestinal tract. We report on an 18-year-old Chinese male who complained with pigmentation on face and extremities for over 10 years. Colonoscopy revealed more than ten polyps from transverse colon to rectum. The family survey included 15 family members from three generations, and 6 PJSs (4 males and 2 females) were found. This case is reported because of its rarity of Peutz-Jeghers syndrome and the survey of family history.

DOI10.1002/anie.201302764
Alternate JournalInt J Clin Exp Pathol