Case ReportInternational Journal of Advances in Medicine

Publication:
Peutz-Jeghers syndrome: a case report

Int J Adv Med. 2015;2(2):175-177.DOI10.5455/2349-3933.ijam20150521

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Abstract

Peutz-Jeghers Syndrome (PJS) is a rare, autosomal dominant disorder responsible for mucocutaneous pigmentation and gastrointestinal hamartomatous polyps. We present a case of Peutz-Jeghers syndrome in a 12 year old male child who presented with abdominal pain, vomiting and malena. The patient had pigmented lesions on the malar area, nose, lower lip and buccal mucosa. The imaging studies revealed multiple polyps in small intestine.

Keywords

Affiliations

  1. Department of Dermatology, Era’s Lucknow Medical College, Lucknow-226003, Uttar Pradesh, India

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