Animal Health Trust, Centre of Small Animal Studies, Newmarket, UK.
Dick White Referrals, Six Mile Bottom, Cambridgeshire, Newmarket, UK.
J Feline Med Surg. 2024 Jan;26(1):1098612X231216636. doi: 10.1177/1098612X231216636.
Angiosarcomas are rare malignant mesenchymal neoplasms of endothelial cell origin with a predilection to the ventral abdominal wall in cats. Larger case series describing this entity are lacking.
Two referral centre laboratory databases were searched for angiosarcoma of the ventral abdominal wall. Nine cases with a histological diagnosis were included. Immunohistochemistry (factor VIII and PROX-1 antibodies) was used to phenotype them as haemangiosarcoma or lymphangiosarcoma.
All cats presented with a ventral abdominal mass, five of which were producing a serosanguinous discharge. Eight underwent tumour staging and pulmonary metastases were suspected in one cat (but not histologically confirmed). With histopathology alone, a diagnosis of angiosarcoma and lymphangiosarcoma was made in four and five cases, respectively. After immunohistochemistry, five cases had a haemangiosarcoma phenotype and four had a lymphangiosarcoma phenotype, including two cases of lymphangiosarcoma that were reclassified as hemangiosarcoma. Eight cats received treatment (either surgery with or without adjuvant therapies or medical management alone). Six cats were euthanased due to local disease progression. The median survival time for haemangiosarcoma was 166 days (range 137-381), and for lymphangiosarcoma it was 197 days (range 67-208). Two cats with haemangiosarcoma remained alive for a follow-up period of 329 and 580 days, respectively.
Feline ventral abdominal angiosarcomas are rare locally aggressive neoplasms. While histology often provides a diagnosis of angiosarcoma, immunohistochemistry is ultimately required to differentiate between haemangiosarcoma and lymphangiosarcoma phenotypes. Further studies are required to evaluate whether the different phenotypes have an impact on treatment response and outcome.
血管肉瘤是一种罕见的起源于内皮细胞的恶性间叶性肿瘤,在猫中倾向于发生于腹侧腹壁。缺乏对此实体的更大病例系列描述。
在两个转诊中心的实验室数据库中搜索腹侧腹壁的血管肉瘤。纳入了 9 例具有组织学诊断的病例。使用免疫组织化学(VIII 因子和 PROX-1 抗体)对其进行表型鉴定为血管肉瘤或淋巴管肉瘤。
所有猫均表现出腹侧腹部肿块,其中 5 例伴有浆液血性分泌物。8 例进行了肿瘤分期,1 例猫疑似有肺转移(但未通过组织学证实)。仅凭组织病理学检查,分别在 4 例和 5 例中做出了血管肉瘤和淋巴管肉瘤的诊断。经过免疫组织化学检查,5 例为血管肉瘤表型,4 例为淋巴管肉瘤表型,包括 2 例重新分类为血管肉瘤的淋巴管肉瘤。8 只猫接受了治疗(手术加或不加辅助治疗或单独药物治疗)。由于局部疾病进展,有 6 只猫被安乐死。血管肉瘤的中位生存时间为 166 天(范围 137-381),淋巴管肉瘤为 197 天(范围 67-208)。2 只患有血管肉瘤的猫分别存活了 329 天和 580 天。
猫的腹侧腹壁血管肉瘤是罕见的局部侵袭性肿瘤。虽然组织学通常可以提供血管肉瘤的诊断,但最终需要免疫组织化学来区分血管肉瘤和淋巴管肉瘤表型。需要进一步研究以评估不同表型是否对治疗反应和预后有影响。