Acute abdomen in a 6 year old disclosed as an inherited autosomal disorder: A case report

Journal Title: Scholars Journal of Medical Case Reports - Year 2017, Vol 5, Issue 3

Abstract

Abstract: A rare syndrome presenting with muco-cutaneous pigmentation with hamartomatous polyposis of intestine associated with increased risk of gastrointestinal and other systemic malignancies popularly termed as Peutz- Jeghers Syndrome present as varied course of symptoms, some report to dermatologist for pigmented oral macules, some report in emergency with acute abdomen while others are diagnosed incidentally. We report a 6 years old male child brought to emergency department with acute abdomen subsequently diagnosed with intussusception caused by a hamartomatous polyp which later on combined with pigmented macules on buccal mucosa ended up as an autosomal dominant syndrome. Keywords: Hamartomatous polyp, intussception, target sign, bilious vomiting.

Authors and Affiliations

Harijot Singh, Rajwinder Kaur, Kulbir Kaur

Keywords

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  • EP ID EP379480
  • DOI -
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How To Cite

Harijot Singh, Rajwinder Kaur, Kulbir Kaur (2017). Acute abdomen in a 6 year old disclosed as an inherited autosomal disorder: A case report. Scholars Journal of Medical Case Reports, 5(3), 138-140. https://europub.co.uk/articles/-A-379480