# Primary Hepatic Hemangiosarcoma With Hemoperitoneum in a Dog: Clinical Course and Therapeutic Outcome

**Authors:** Myeong-Yeon Lee, Jong-Hyun Moon, Jinsu Mok, Dowoo Lim, Ju-Yeong Kim, Seo-Yeong Jung, Eunbin Jeong, Hyomi Jang, Dong-In Jung

PMC · DOI: 10.1155/crve/8709546 · Case Reports in Veterinary Medicine · 2026-01-28

## TL;DR

A dog with a rare liver tumor survived 201 days after surgery and chemotherapy, showing the aggressive nature of the disease and treatment challenges.

## Contribution

This case report provides insights into the clinical management and receptor expression patterns of primary hepatic hemangiosarcoma in a dog.

## Key findings

- The dog survived 201 days following a multimodal treatment approach.
- Postmortem analysis revealed heterogeneous receptor tyrosine kinase expression in the tumor.
- The case highlights the aggressive metastatic behavior of primary hepatic hemangiosarcoma.

## Abstract

A 14‐year‐old neutered male mixed‐breed dog presented with hemoperitoneum secondary to rupture of a primary hepatic mass. Following stabilization with whole blood transfusion, a hepatic lobectomy was performed. Histopathological examination and CD31 immunolabeling confirmed a diagnosis of hemangiosarcoma. Two weeks postoperatively, multiple intra‐abdominal metastases were identified. The multimodal therapeutic approach included one attempted VAC cycle (discontinued due to Grade 4 neutropenia), five cycles of single‐agent doxorubicin, and subsequent administration of toceranib with dose reduction for anemia. The dog survived 201 days after diagnosis. Postmortem extended immunohistochemistry demonstrated heterogeneous receptor tyrosine kinase (RTK) expression: EGFR and VEGFR positivity, strong membranous HER2 labeling in approximately 60% of tumor cells, low KIT expression, and negative PDGFR. This case underscores the aggressive metastatic nature of primary hepatic hemangiosarcoma following rupture and highlights practical considerations for systemic therapy selection and adverse event monitoring in clinical practice.

## Linked entities

- **Proteins:** PECAM1 (platelet and endothelial cell adhesion molecule 1), EGFR (epidermal growth factor receptor), KDR (kinase insert domain receptor), ERBB2 (erb-b2 receptor tyrosine kinase 2), KIT (KIT proto-oncogene, receptor tyrosine kinase), PDGFRB (platelet derived growth factor receptor beta)
- **Chemicals:** doxorubicin (PubChem CID 31703), toceranib (PubChem CID 5329106)
- **Diseases:** hemangiosarcoma (MONDO:0016982)
- **Species:** Canis lupus familiaris (taxon 9615)

## Full-text entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 404306], ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 403883] {aka HER-2, c-erbB-2, p185erbB2}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 403811] {aka c-KIT}
- **Diseases:** Hemoperitoneum (MESH:D006465), metastases (MESH:D009362), Hepatic Hemangiosarcoma (MESH:D006394), tumor (MESH:D009369), anemia (MESH:D000740), hepatic mass (MESH:C536030), rupture (MESH:D012421), neutropenia (MESH:D009503)
- **Chemicals:** VAC (-), doxorubicin (MESH:D004317)
- **Species:** Canis lupus familiaris (dog, subspecies) [taxon 9615]

## Full text

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## Figures

16 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12848542/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12848542/full.md

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Source: https://tomesphere.com/paper/PMC12848542