Lenz J A, Furrow E, Craig L E, Cannon C M
Department of Clinical Sciences, College of Veterinary Medicine, University of Tennessee, Knoxville, Tennessee, 37996, USA.
Department of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, Minnesota, 55455, USA.
J Small Anim Pract. 2017 Aug;58(8):461-467. doi: 10.1111/jsap.12688. Epub 2017 May 25.
To describe a series of miniature schnauzers diagnosed with histiocytic sarcoma and assess for possible breed predisposition.
Medical records of miniature schnauzers with a diagnosis of histiocytic sarcoma between January 2008 and April 2015 were reviewed. Data collected included signalment, body weight, presenting complaint, date of diagnosis, clinicopathologic and diagnostic imaging findings, treatment, therapeutic response, date of death or last follow-up and necropsy findings. Breed predisposition was assessed with odds ratios, using breed-matched dogs without histiocytic sarcoma admitted during the study period as controls. Pedigree analysis was performed for dogs with available registration information.
Fourteen miniature schnauzers were diagnosed with histiocytic sarcoma during the study period, making them over-represented among the hospital population (odds ratio=4·8, P=0·0009). Disease was considered localised in ten dogs and disseminated in four. Of the dogs with localised disease, nine were diagnosed with primary pulmonary histiocytic sarcoma based on the presence of a large pulmonary mass with (n=7) or without (n=2) evidence of intra-thoracic metastasis, and one had gastric histiocytic sarcoma with nodal metastasis. Treatments varied, but an aggressive clinical course was found in most patients. Pedigree analysis revealed a recent common ancestor for a subset of the dogs assessed.
Miniature schnauzers were over-represented among dogs with histiocytic sarcoma in this patient population. Pedigree analysis supports an inherited risk factor, which has not previously been suggested in the breed. Primary pulmonary involvement with or without intra-thoracic metastasis was common in this cohort.
描述一系列被诊断为组织细胞肉瘤的迷你雪纳瑞犬,并评估是否存在可能的品种易感性。
回顾了2008年1月至2015年4月间被诊断为组织细胞肉瘤的迷你雪纳瑞犬的病历。收集的数据包括信号特征、体重、就诊主诉、诊断日期、临床病理和诊断影像学检查结果、治疗方法、治疗反应、死亡日期或最后随访情况以及尸检结果。使用比值比评估品种易感性,以研究期间收治的无组织细胞肉瘤的品种匹配犬作为对照。对有可用登记信息的犬进行系谱分析。
在研究期间,14只迷你雪纳瑞犬被诊断为组织细胞肉瘤,使其在医院犬只群体中占比过高(比值比=4·8,P=0·0009)。疾病被认为局限于10只犬,播散于4只犬。在局限型疾病的犬中,9只基于存在大的肺部肿块(有(n=7)或无(n=2)胸内转移证据)被诊断为原发性肺组织细胞肉瘤,1只患有胃组织细胞肉瘤伴淋巴结转移。治疗方法各不相同,但大多数患者的临床病程较为凶险。系谱分析显示,所评估的部分犬有一个近期的共同祖先。
在该患者群体中,迷你雪纳瑞犬在患有组织细胞肉瘤的犬中占比过高。系谱分析支持存在遗传风险因素,此前该品种未被提及过这一点。在这一队列中,原发性肺部受累伴或不伴胸内转移很常见。