دورية أكاديمية
Ileo-ileal intussusception secondary to a Peutz-Jeghers hamartomatous polyp in an infant.
| العنوان: | Ileo-ileal intussusception secondary to a Peutz-Jeghers hamartomatous polyp in an infant. |
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| المؤلفون: | Neville JJ; Department of Paediatric Surgery, Royal Alexandra Children's Hospital, Brighton, UK jonathan.neville@nhs.net., Ellul S; Department of Paediatric Surgery, Royal Alexandra Children's Hospital, Brighton, UK., Healy C; Department of Paediatric Surgery, Royal Alexandra Children's Hospital, Brighton, UK. |
| المصدر: | BMJ case reports [BMJ Case Rep] 2024 Jul 25; Vol. 17 (7). Date of Electronic Publication: 2024 Jul 25. |
| نوع المنشور: | Case Reports; Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: BMJ Pub. Group Country of Publication: England NLM ID: 101526291 Publication Model: Electronic Cited Medium: Internet ISSN: 1757-790X (Electronic) Linking ISSN: 1757790X NLM ISO Abbreviation: BMJ Case Rep Subsets: MEDLINE |
| أسماء مطبوعة: | Original Publication: London : BMJ Pub. Group |
| مواضيع طبية MeSH: | Intussusception*/etiology , Intussusception*/surgery , Intussusception*/diagnosis , Peutz-Jeghers Syndrome*/complications , Peutz-Jeghers Syndrome*/surgery , Peutz-Jeghers Syndrome*/diagnosis , Ileal Diseases*/surgery , Ileal Diseases*/etiology , Ileal Diseases*/diagnosis , Hamartoma*/surgery , Hamartoma*/complications , Hamartoma*/diagnosis, Humans ; Male ; Infant ; Diagnosis, Differential ; Intestinal Polyps/complications ; Intestinal Polyps/surgery |
| مستخلص: | We report the case of ileo-ileal intussusception secondary to a Peutz-Jeghers syndrome (PJS) hamartomatous polyp in a male infant. The patient presented with non-bilious vomiting and a single episode of passing blood in his stool. An upper gastrointestinal contrast study showed proximal bowel obstruction. At laparotomy, ileo-ileal intussusception was identified with a papillary mass acting as a lead point. The mass was resected, and a primary anastomosis was performed. The patient recovered well and was discharged on postoperative day 5. Histological assessment diagnosed a PJS hamartoma. The patient was well at 1 month follow-up. This case report describes a rare cause of intussusception in an infant that should be considered in the differential diagnosis. The diagnosis of PJS in infancy is uncommon and requires long-term follow-up. Competing Interests: Competing interests: None declared. (© BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ.) |
| فهرسة مساهمة: | Keywords: Infant health; Paediatric Surgery; Pediatrics; Small intestine |
| تواريخ الأحداث: | Date Created: 20240726 Date Completed: 20240727 Latest Revision: 20240727 |
| رمز التحديث: | 20240729 |
| DOI: | 10.1136/bcr-2024-261464 |
| PMID: | 39059798 |
| قاعدة البيانات: | MEDLINE |
Full Text Finder | تدمد: | 1757-790X |
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| DOI: | 10.1136/bcr-2024-261464 |