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Multifocal Necrotizing Myopathy in Northern Elephant Seal (Mirounga angustirostris) Pups, San Miguel Island, California

机译:北大象封印(Mirounga angustriostris)幼崽的多焦点肌病(Mirounga angustristris)幼崽,圣米格尔岛,加利福尼亚州

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摘要

A field study addressing causes of mortality in freshly dead northern elephant seals (Mirounga angustirostris, Gill, 1866) was conducted on San Miguel Island, California, in February 2015. Necropsies were performed on 18 pups ranging in age from stillbirths to approximately 7 to 8 weeks. The primary gross diagnoses in these pups included trauma, myopathy, starvation/emaciation, infections, congenital anomalies, and perinatal mortality. However, 6 (33%) had a previously unrecognized myopathy characterized by multiple white streaks that were most obvious within the inner layer of the abdominal wall and the small innermost ventral intercostal muscles. Following histological examination, 2 more pups from San Miguel Island and 6 pups from The Marine Mammal Center (Sausalito, California) were found to have similar lesions. Histologically, the lesions within the skeletal muscles were characterized by a multifocal polyphasic, mild to severe, acute to subacute necrotizing myopathy with mineralization. Acute necrosis and degeneration characterized by pyknotic nuclei, eosinophilic cytoplasm and cytoplasmic vacuolization were found in smooth muscle myocytes within the urinary bladder and digestive system. Degeneration of myocytes was present in the tunica media of a few small- to medium-sized vessels and was characterized by a vacuolar degeneration and occasionally necrosis. This condition has been termed multifocal necrotizing myopathy. A cause of this myopathy was not identified.
机译:在2015年2月在加利福尼亚州圣米格尔岛(Mirounga Angustris,Gill,Gill,1866)上进行了野外研究结果,在2015年2月在圣米格尔斯岛进行。尸检是在18只幼崽,从死产的年龄达到约7至8次进行周。这些幼崽中的主要诊断包括创伤,肌病,饥饿/解剖,感染,先天性异常和围产期死亡率。然而,6(33%)具有以前未被识别的肌病,其特征在于多个白色条纹,在腹壁内层和小型内侧腹膜肌内最明显。组织学检查后,发现来自San Miguel Island的更多幼犬和来自海洋哺乳动物中心的6只幼犬(加利福尼亚州Sausalito)有类似的病变。组织学上,骨骼肌内的病变是通过多焦点多相,轻度至严重,急性对血栓化的矿物质化的表征。通过Pyknotic核,嗜酸性细胞质和细胞质真空表征的急性坏死和变性在膀胱和消化系统中的平滑肌肌细胞中发现。肌细胞的退化存在于少量小于中等血管的丘脑培养基中,其特征在于真空退化和偶尔坏死。这种情况被称为多焦点坏死性肌病。没有发现这种肌病的原因。

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