一例金毛猎犬肝脏组织细胞肉瘤的多模态诊疗与长期生存分析
Multimodal Diagnosis, Treatment and Long-Term Survival Analysis of a Primary Hepatic Histiocytic Sarcoma in a Golden Retriever
DOI: 10.12677/acrpvm.2025.144006, PDF,   
作者: 向小松*, 刘 洋:上海小王子宠物医院周东路分院,上海;耿丹丹#, 王思思, 董文亚:上海每诺家宠物医院,上海;庄 皓:华中农业大学动物医学院,湖北 武汉
关键词: 肝脏组织细胞肉瘤超声造影磁共振成像帕唑帕尼长期生存多模式治疗Hepatic Histiocytic Sarcoma Canine Contrast-Enhanced Ultrasonography Magnetic Resonance Imaging Pazopanib Long-Term Survival Multimodal Therapy
摘要: 目的(Objective):探讨多模态诊疗策略对犬原发性肝脏组织细胞肉瘤(HHS)的诊疗价值及生存获益。方法(Methods):报告一例14岁雄性绝育金毛猎犬病例。通过体格检查、实验室检查(血常规、生化、CRP)、多模态影像学(X线、超声、超声造影CEUS、磁共振MRI)、细胞学及组织病理学确诊为原发性HHS。先行肿瘤细胞减灭术(减瘤率 > 85%),术后14天启动口服酪氨酸激酶抑制剂帕唑帕尼(3 mg/kg, Q24H)以抑制血管生成,术后第14天加用多柔比星化疗(30 mg/m2,Q3W,共5周期)。不良反应监测方案:化疗前/后48小时全血细胞计数(骨髓抑制);血压测量(Q2W);尿蛋白肌酐比(UPCR, Q4W);肝功能(ALT/ALKP, Q4W);心脏超声(每2周期)。结果(Results):患犬呈现食欲废绝、咳嗽、脓血性鼻涕及腹部肿块。实验室检查提示贫血、肝损伤及炎症。CEUS显示肝脏占位动脉期环状高增强,门脉期快速廓清(>40%/min,“快进快出”模式)。MRI显示T1WI稍低信号、T2WI/STIR中高信号、DWI高信号(弥散受限),动态增强呈“快进快出”。细胞学及组织病理学确诊为恶性组织细胞肉瘤。术后联合治疗耐受性良好,未出现严重高血压(收缩压 < 160 mmHg)、蛋白尿(UPCR < 0.5)或肝毒性。确诊后总生存期(OS)达456天。确诊后15个月并发鼻腔鳞状上皮癌,最终实施安乐死。结论(Conclusion):本例表明,手术减瘤联合多柔比星化疗及帕唑帕尼靶向治疗的多模式方案,可能显著延长犬HHS生存期(较文献报道多柔比星单药方案中位生存期(169天)提升268%)。多模态影像(CEUS, MRI)对HHS的术前诊断和评估具有重要价值。老年犬肿瘤管理中需警惕化疗相关继发癌变风险。
Abstract: Objective: To evaluate the diagnostic value and survival benefits of a multimodal strategy for canine primary hepatic histiocytic sarcoma (HHS). Methods: A 14-year-old castrated male Golden Retriever was diagnosed with primary HHS via physical examination, laboratory tests (CBC, serum biochemistry, CRP), multimodal imaging (radiography, ultrasonography, contrast-enhanced ultrasonography [CEUS], magnetic resonance imaging [MRI]), cytology, and histopathology. The treatment protocol was designed based on cytoreductive enhancement theory: Cytoreductive surgery (>85% cytoreduction rate) was performed first, followed by oral pazopanib (tyrosine kinase inhibitor; 3 mg/kg, Q24H) initiated on postoperative day 14 to inhibit angiogenesis. Doxorubicin chemotherapy (30 mg/m2, Q3W, 5 cycles) commenced on postoperative day 14. Adverse event monitoring included: CBC 48 h pre/post-chemotherapy (myelosuppression); blood pressure Q2W; UPCR (urine protein-to-creatinine ratio) Q4W; hepatic enzymes (ALT/ALKP) Q4W; echocardiography every 2 cycles. Results: The dog presented with anorexia, cough, purulent/bloody nasal discharge, and an abdominal mass. Laboratory findings revealed anemia, hepatic injury, and inflammation. CEUS showed ring-like hyperenhancement in the arterial phase and rapid washout (>40%/min, “wash-in/wash-out” pattern) in the portal phase. MRI demonstrated: hypointense T1WI, hyperintense T2WI/STIR, restricted diffusion on DWI, and dynamic “wash-in/wash-out” enhancement. Cytology/histopathology confirmed malignant HS. The combined therapy was well-tolerated without significant hypertension (SBP < 160 mmHg), proteinuria (UPCR < 0.5), or hepatotoxicity. Overall survival (OS) was 456 days. Nasal squamous cell carcinoma developed at 15 months post-diagnosis, leading to euthanasia. Conclusion: Cytoreductive surgery combined with doxorubicin and pazopanib significantly prolonged survival in canine HHS (268% increase versus literature-reported median survival of 169 days with doxorubicin monotherapy). Multimodal imaging (CEUS, MRI) provides critical preoperative diagnostic and staging information. Vigilance for chemotherapy-associated secondary carcinogenesis is essential in geriatric canine oncology.
文章引用:向小松, 刘洋, 耿丹丹, 王思思, 董文亚, 庄皓. 一例金毛猎犬肝脏组织细胞肉瘤的多模态诊疗与长期生存分析[J]. 亚洲兽医病例研究, 2025, 14(4): 43-50. https://doi.org/10.12677/acrpvm.2025.144006

参考文献

[1] Moore, P.F. (2014) A Review of Histiocytic Diseases of Dogs and Cats. Veterinary Pathology, 51, 167-184. [Google Scholar] [CrossRef] [PubMed]
[2] Kennedy, K., Thomas, R. and Breen, M. (2016) Canine Histiocytic Malignancies—Challenges and Opportunities. Veterinary Sciences, 3, Article 2. [Google Scholar] [CrossRef] [PubMed]
[3] Affolter, V.K. and Moore, P.F. (2002) Localized and Disseminated Histiocytic Sarcoma of Dendritic Cell Origin in Dogs. Veterinary Pathology, 39, 74-83. [Google Scholar] [CrossRef] [PubMed]
[4] Doka, R.M., Suter, S.E., Mastromauro, M.L., Bennett, A.L. and Hess, P.R. (2022) Doxorubicin for Treatment of Histiocytic Sarcoma in Dogs: 31 Cases (2003-2017). Journal of the American Veterinary Medical Association, 260, 1827-1833. [Google Scholar] [CrossRef] [PubMed]
[5] Latifi, M., Tuohy, J.L., Coutermarsh‐Ott, S.L., Klahn, S.L., Leeper, H. and Dervisis, N. (2020) Clinical Outcomes in Dogs with Localized Splenic Histiocytic Sarcoma Treated with Splenectomy with or without Adjuvant Chemotherapy. Journal of Veterinary Internal Medicine, 34, 2645-2650. [Google Scholar] [CrossRef] [PubMed]
[6] Gomez, N.U., Rossi, F., Rademacher, N., et al. (2021) Contrast-Enhanced Ultrasound of Canine Hepatic Tumors. Veterinary Radiology & Ultrasound, 62, 298-306.
[7] Owen, L.N. (1980) TNM Classification of Tumors in Domestic Animals. WHO.
[8] Kato, Y., Murakami, M., Hoshino, Y., et al. (2020) MRI Characteristics of Canine Histiocytic Sarcoma. Journal of Veterinary Medical Science, 82, 589-595.
[9] Lamb, C.R., Ciasca, T.C., Mantis, P., et al. (2016) MRI Features of Primary Hepatic Tumors in Dogs. Veterinary Radiology & Ultrasound, 57, 362-371.
[10] Giori, L., Caleri, E., Faverzani, S., et al. (2021) Contrast-Enhanced Ultrasonography vs Magnetic Resonance for Focal Liver Lesions. Frontiers in Veterinary Science, 8, Article 689543.
[11] Safai Zadeh, E., Dietrich, C.F., Dong, Y., et al. (2023) WFUMB CEUS Guidelines: Rare Malignant Mesenchymal Liver Lesions. Med Ultrasonogram, 25, 456-467.
[12] London, C.A., Malpas, P.B., Wood-Follis, S.L., et al. (2012) Multi-Center, Placebo-Controlled, Double-Blind, Randomized Study of Oral Toceranib Phosphate for Recurrent Osteosarcoma. Veterinary and Comparative Oncology, 11, 306-315.
[13] Marconato, L., Sabattini, S., Marisi, G., et al. (2023) Multi-Target Tyrosine Kinase Inhibitor in Canine Histiocytic Sarcoma. Veterinary and Comparative Oncology, 21, 123-131.
[14] Fowles, J.S., Dawn, M. and Cicking, D. (2020) Doxorubicin Induces TP53 Mutations in Canine Cancers. Veterinary and Comparative Oncology, 18, 315-323.
[15] Pang, L.Y. and Argyle, D.J. (2023) Telomere Shortening and DNA Damage in Aged Dogs with Cancer. The Veterinary Journal, 291, Article ID: 105919.