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Appendiceal Neuroendocrine Tumor Mimicking Acute Appendicitis
N Gautam1, R Makaju1, D Basnet1
1Department of Pathology, Dhulikhel Hospital, Kathmandu University Hospital, Kathmandu University School of Medical Sciences, Dhulikhel, Kavre, Nepal.
Appendiceal carcinoid tumors are common, often presenting as acute appendicitis. This case highlights a neuroendocrine tumor of the appendix, diagnosed via histopathology and immunohistochemistry.
Area of Science:
- Gastroenterology and Oncology
- Pathology
Background:
- Appendiceal carcinoids represent the most common tumors of the appendix, accounting for 32-57% of all appendiceal neoplasms.
- Neuroendocrine tumors are a significant category within appendiceal neoplasms.
Observation:
- A case presented with symptoms mimicking acute appendicitis.
- Gross examination revealed appendiceal tip perforation with a 30 ml periappendicular collection.
- Histopathological analysis identified a carcinoid tumor infiltrating the muscularis propria and subserosa.
Findings:
- Tumor cells were arranged in tubules, acini, and nests.
- Immunohistochemistry confirmed the diagnosis with positive Synaptophysin staining.
- A Ki-67 labeling index of 2% indicated low proliferative activity.
- Absence of perineural and vascular invasion was noted.
Implications:
- This case underscores the importance of considering appendiceal neuroendocrine tumors in the differential diagnosis of acute appendicitis.
- Accurate diagnosis through histopathology and immunohistochemistry is crucial for appropriate patient management.
- Understanding the presentation and characteristics of appendiceal carcinoids aids in clinical decision-making.
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