Peutz-Jeghers syndrome: A case report

Authors

DOI:

https://doi.org/10.3126/ajms.v12i7.35064

Keywords:

Intussusception, mucocutaneous pigmentation, Peutz-Jeghers syndrome, tubulovillous adenoma

Abstract

Peutz-jeghers syndrome is a rare inherited autosomal dominant disease which is characterized by mucocutaneous pigmentation and multiple polyps in the gastrointestinal tract. We report a case of 10 years old female who was referred to us from surgical department for the evaluation of brownish pigmented macules over lips, face, palms and soles. Patient was presented with recurrent abdominal pain along with vomiting and blood mixed stool for a month. Ultrasound of abdomen revealed jejuno-jejunal intussusception for which laparotomy was done during which multiple polyps were visualized. Polypectomy was done and biopsy revealed it to be tubulovillous adenoma. Patient was diagnosed as Peutz-jeghers syndrome as there were multiple polyps in the jejunum along with the characteristics mucocutaneous involvement.

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Published

2021-07-01

How to Cite

Poudel, P., & Jahan, R. (2021). Peutz-Jeghers syndrome: A case report. Asian Journal of Medical Sciences, 12(7), 154–156. https://doi.org/10.3126/ajms.v12i7.35064

Issue

Vol. 12 No. 7 (2021)

Section

Case Reports

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