Jacinto Joana G P, Häfliger Irene M, Borel Nicole, Zanolari Patrik, Drögemüller Cord, Veiga Inês M B
Department of Veterinary Medical Sciences, University of Bologna, 40064 Ozzano Emilia (BO), Italy.
Institute of Genetics, Vetsuisse Faculty, University of Bern, 3012 Bern, Switzerland.
Animals (Basel). 2021 Feb 26;11(3):624. doi: 10.3390/ani11030624.
Bovine juvenile angiomatosis (BJA) comprises a group of single or multiple proliferative vascular anomalies in the skin and viscera of affected calves. The purpose of this study was to characterize the clinicopathological phenotype of a 1.5-month-old Simmental calf with multiple cutaneous, subcutaneous, and visceral vascular hamartomas, which were compatible with a generalized form of BJA, and to identify genetic cause for this phenotype by whole-genome sequencing (WGS). The calf was referred to the clinics as a result of its failure to thrive and the presence of multiple cutaneous and subcutaneous nodules, some of which bled abundantly following spontaneous rupture. Gross pathology revealed similar lesions at the inner thoracic wall, diaphragm, mediastinum, pericardium, inner abdominal wall, and mesentery. Histologically, variably sized cavities lined by a single layer of plump cells and supported by a loose stroma with occasional acute hemorrhage were observed. Determined by immunochemistry, the plump cells lining the cavities displayed a strong cytoplasmic signal for PECAM-1, von Willebrand factor, and vimentin. WGS revealed six private protein-changing variants affecting different genes present in the calf and absent in more than 4500 control genomes. Assuming a spontaneous de novo mutation event, one of the identified variants found in the and genes may represent a possible candidate pathogenic variant for this rare form of vascular malformation.
牛幼年血管瘤病(BJA)是指受影响犊牛皮肤和内脏中出现的一组单发或多发的增殖性血管异常。本研究的目的是对一头1.5月龄西门塔尔犊牛的临床病理表型进行特征描述,该犊牛患有多处皮肤、皮下和内脏血管错构瘤,符合广义形式的BJA,并通过全基因组测序(WGS)确定该表型的遗传原因。这头犊牛因生长发育不良以及存在多处皮肤和皮下结节而被转诊至诊所,其中一些结节在自发破裂后大量出血。大体病理学检查显示,在内胸壁、膈肌、纵隔、心包、内腹壁和肠系膜处有类似病变。组织学检查发现,有大小不一的腔隙,内衬单层丰满细胞,由疏松的间质支撑,偶见急性出血。免疫组化检测显示,腔隙内衬的丰满细胞对血小板内皮细胞黏附分子-1(PECAM-1)、血管性血友病因子和波形蛋白呈现强细胞质信号。WGS揭示了6个影响犊牛中不同基因的私有蛋白改变变体,在4500多个对照基因组中未发现这些变体。假设发生自发的新生突变事件,在 和 基因中发现的一个已识别变体可能是这种罕见血管畸形形式的一个可能候选致病变体。