# A Rare Case of a Primary Isolated Intraperitoneal Teratoma With a Yolk Sac Tumor Component in a Three-Year-Old Boy

**Authors:** Raj M Dongol, Neera Pathak, Moni Subedi

PMC · DOI: 10.7759/cureus.95115 · Cureus · 2025-10-21

## TL;DR

A three-year-old boy was diagnosed with a rare intraperitoneal teratoma containing a yolk sac tumor and successfully treated with surgery and chemotherapy.

## Contribution

This paper presents a rare clinical case of a primary isolated intraperitoneal teratoma with a yolk sac tumor component in a child.

## Key findings

- Complete surgical excision followed by chemotherapy led to a favorable outcome in the patient.
- Histopathological evaluation is crucial for identifying malignant components like yolk sac tumors in teratomas.
- The case highlights the diagnostic challenges in managing teratomas with malignant elements.

## Abstract

Primary isolated intraperitoneal teratoma is an exceptionally rare entity, and the presence of a yolk sac tumor component within it is even more uncommon. We report a case of a three-year-old boy diagnosed with a primary isolated intraperitoneal teratoma containing a yolk sac tumor component. The patient underwent complete surgical excision followed by adjuvant chemotherapy, with a favorable clinical outcome. Histopathological evaluation of teratomas with malignant components poses a significant diagnostic challenge, underscoring the critical role of identifying malignant elements such as yolk sac tumor to guide appropriate management.

## Linked entities

- **Diseases:** yolk sac tumor (MONDO:0002143), teratoma (MONDO:0002601)

## Full-text entities

- **Diseases:** Intraperitoneal Teratoma (MESH:D013724), Yolk Sac Tumor (MESH:D018240)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12635501/full.md

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Source: https://tomesphere.com/paper/PMC12635501