# Clinicopathological Profile and Management of Appendiceal Neoplasm: An Observational Study

**Authors:** Abhishek Bhattarai, Prasan Bir Singh Kansakar, Laligen Awale, Bikal Ghimire, Homendra Kumar Sah

PMC · DOI: 10.31729/jnma.63.290.9206 · JNMA: Journal of the Nepal Medical Association · 2025-09-01

## TL;DR

This study examines the characteristics and treatment outcomes of rare appendiceal tumors diagnosed in Nepal, finding that most cases had good outcomes despite some postoperative complications.

## Contribution

The study provides a detailed clinicopathological analysis of appendiceal neoplasms in Nepal, highlighting trends in diagnosis and treatment outcomes.

## Key findings

- Mucinous tumors were the most common type of appendiceal neoplasm identified.
- Appendectomy was sufficient for most cases, with few requiring further surgery.
- Outcomes were generally favorable despite some postoperative complications.

## Abstract

Appendiceal neoplasms are rare and frequently diagnosed incidentally during histopathological examination of appendectomy specimens. Recent data suggest that their incidence is increasing worldwide. This study aimed to evaluate the appendiceal neoplasm in appendectomy specimens, determine their clinicopathological presentation, histological subtypes, diagnostic modalities used, and the outcomes at the Tribhuvan University Teaching Hospital, Kathmandu, Nepal.

A retrospective evaluation of patients diagnosed with appendiceal neoplasm was conducted from January 2013 to December 2023 at Tribhuvan University Teaching Hospital in Kathmandu, Nepal. Ethical approval was obtained from the Institutional Review Board (Ethical Approval Reference No: 32081/082). Various parameters, including demographic profiles, disease pathology and outcomes were studied.

A total of 57 cases of appendiceal neoplasm were identified during the study period. The mean age at diagnosis was 47.1±18.5 years. Among them, 29 (50.87%) were male and 28 (49.12%) were female. Of the total cases, 52 (91.22%) cases were primary appendiceal neoplasms, 3 (5.26%) were secondary, and 2 (3.50%) cases remained unclassified. The primary mucinous appendiceal neoplasm was seen in 43 (75.44%), followed by neuroendocrine tumor in 5 (8.77%) cases. Appendectomy was performed in 29 (50.88%) and right hemicolectomy in 15 (26.32%) cases. The major perioperative complications were observed in 2 (3.50%) cases, with 1 (1.75%) case of mortality.

The number of diagnosed appendiceal neoplasms increased over the year with mucinous tumors being predominant followed by neuroendocrine tumor. Appendectomy was adequate in most cases, with limited need for further surgery, and outcomes remain excellent despite few of them developed major postoperative complications.

## Linked entities

- **Diseases:** appendiceal neoplasm (MONDO:0001236)

## Full-text entities

- **Diseases:** signet ring cell adenocarcinomas (MESH:D018279), GCA (MESH:D002292), Lymphoma (MESH:D008223), polyp (MESH:D011127), chronic pain (MESH:D059350), gastrointestinal neoplasms (MESH:D005770), intestinal obstruction (MESH:D007415), perforation (MESH:D057112), non Hodgkins lymphoma (MESH:D008228), mucinous adenocarcinoma (MESH:D002288), infection (MESH:D007239), postoperative complication (MESH:D011183), anastomotic leaks (MESH:D057868), adeno-neuroendocrine carcinoma (MESH:D018278), acute appendicitis (MESH:D001064), epithelial neoplasms (MESH:D009375), metastases (MESH:D009362), intussusception (MESH:D007443), pseudomyxoma peritonei (MESH:D011553), NET (MESH:D018358), colonic carcinoma (MESH:D003110), chest infections (MESH:D002637), HIPEC (MESH:D000084202), AN (MESH:D001063), Mucinous neoplasms (MESH:D018297), Peritoneal Carcinomatosis (MESH:D010534), cancer (MESH:D009369), adenocarcinoma (MESH:D000230), ileocecal mass (MESH:D044504), epithelial tumors (MESH:D002277), bowel obstruction (MESH:D012778), pain (MESH:D010146), RIF (MESH:D017543)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12860671/full.md

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Source: https://tomesphere.com/paper/PMC12860671