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DOI 10.1016/j.ijscr.2024.109606

Медицинская библиотека · International journal of surgery case reports · 2024

Ileal duplication in adults: A rare case.

Zaiem Aida, Atri Souhaib, Fteriche Fadhel Samir, Frikha Wassim, Haddad Anis, Kacem Montassar

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Аннотация

INTRODUCTION AND

IMPORTANCE

Intestinal duplication is an uncommon congenital malformation affecting the alimentary tract. This article presents a case of enteric duplication cyst (EDC) in an adult, accompanied by a review of the available literature.

CASE PRESENTATION: A 34-year-old woman with polymyositis underwent a routine CT scan as part of her medical assessment revealing an 8 cm mass near the caecum and terminal ileum. Diagnostic procedures confirmed a cystic spherical mass. The patient underwent ileo-cecal resection, with primary anastomosis and an uneventful recovery.

CLINICAL DISCUSSION: Studies indicate that the frequency of polymyositis coexisting with a neoplasm range from 6 % to 40 %. Therefore, a body CT scan is recommended for patients with myopathy as in our patient. Intestinal duplications are predominantly found in children but can also occur in adults, often discovered incidentally or due to complications. Diagnostic imaging techniques, such as ultrasonography and CT scan, are crucial in identifying duplication location and characteristics. In this case, colonoscopy indicated ileocecal valve compression, and histological examination confirmed an enteric duplication cyst with ectopic gastric mucosa.

CONCLUSION

Enteric duplication cysts are rare, and the existing literature on the topic somewhat limited. Early diagnosis and surgical intervention are essential to stave off potential complications and reduce morbidity. Clinician awareness of enteric duplication cysts enables timely management, enhancing patient outcomes. Further research is needed to improve understanding and optimize patient care.

Для цитирования: Zaiem Aida, Atri Souhaib, Fteriche Fadhel Samir, Frikha Wassim, Haddad Anis, Kacem Montassar. Ileal duplication in adults: A rare case.. International journal of surgery case reports. 2024. DOI: 10.1016/j.ijscr.2024.109606.
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