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Published on: August 24, 2019
Xanthogranulomatous appendicitis: A comprehensive literature review
Sami Akbulut1, Khaled Demyati2, Cemalettin Koc2
1Department of Surgery and Liver Transplant Institute, Inonu University Faculty of Medicine, Malatya 44280, Turkey. akbulutsami@gmail.com.
Xanthogranulomatous appendicitis (XGA) is a rare condition presenting diagnostic challenges. This review highlights its variable presentation, association with interval appendectomies, and frequent misdiagnosis as a tumoral lesion.
Area of Science:
- Gastroenterology
- Pathology
- Surgical Oncology
Background:
- Xanthogranulomatous inflammation involves lipid-laden macrophages and inflammatory cells.
- It can mimic neoplastic processes, posing diagnostic challenges.
Purpose of the Study:
- To conduct a literature review on xanthogranulomatous appendicitis (XGA).
- To analyze the clinical presentation, diagnosis, and management of XGA.
Main Methods:
- A comprehensive literature search was performed using PubMed, MEDLINE, Google Scholar, and Google.
- Keywords included "appendix vermiformis," "appendectomy," "acute appendicitis," and "XGA."
- Retrospective analysis of 29 articles involving 38 patients with XGA.
Main Results:
- XGA affects patients aged 3 to 78 years, with a slight female predominance (52.6%).
- 25 patients presented with appendicitis; 13 underwent surgery for ileocecal tumoral lesions.
- 16 patients required interval appendectomy, and some needed bowel resection.
Conclusions:
- Xanthogranulomatous appendicitis is rare and presents diagnostic and therapeutic dilemmas.
- It often mimics tumoral lesions, leading to delayed diagnosis and potential bowel resection.
- XGA is typically diagnosed retrospectively on surgical pathology, lacking unique preoperative features.
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