A 16-Year-Old Female with Peutz-Jeghers Syndrome

Authors

  • Mufti Munsurar Rahman Professor, Department of Medicine, Enam Medical College & Hospital, Savar, Dhaka
  • Mamunur Rashid Registrar, Department of Medicine, Enam Medical College & Hospital, Savar, Dhaka
  • Rukhsana Parvin Associate Professor, Department of Medicine, Enam Medical College & Hospital, Savar, Dhaka
  • Arun Joyati Tarafder Assistant Professor, Department of Hepatology, Mymensingh Medical College & Hospital, Mymensingh

DOI:

https://doi.org/10.3329/jemc.v4i3.20958

Keywords:

Peutz-Jeghers syndrome, Intussusception, Polyps, Circumoral pigmentation

Abstract

Peutz-Jeghers syndrome is a rare autosomal dominant disorder of hamartomatous polyposis of the gastrointestinal tract, with pigmentation around lips and macules on the buccal mucosa that typically manifests itself as recurrent colicky abdominal pain and intestinal obstruction due to intussusception. Here we report a case of a 16-year-old girl who presented with abdominal pain, vomiting and previous history of laparotomy for intussusception. Multiple well demarcated black pigmented macules on lips, perioral region, buccal mucosa, digits, palms and soles were noted. She was diagnosed as a case of Peutz-Jeghers syndrome and managed conservatively.

DOI: http://dx.doi.org/10.3329/jemc.v4i3.20958

J Enam Med Col 2014; 4(3): 184-187

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Published

2014-11-25

How to Cite

Rahman, M. M., Rashid, M., Parvin, R., & Tarafder, A. J. (2014). A 16-Year-Old Female with Peutz-Jeghers Syndrome. Journal of Enam Medical College, 4(3), 184–187. https://doi.org/10.3329/jemc.v4i3.20958

Issue

Vol. 4 No. 3 (2014)

Section

Case Reports

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