Azargoun Reza, Hashemi-Asl Seyed Mohammad, Asri-Rezaei Siamak
Department of Internal Medicine and Clinical Pathology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.
Department of Surgery and Diagnostic Imaging, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.
Vet Res Forum. 2024;15(4):215-218. doi: 10.30466/vrf.2024.2011964.4014. Epub 2024 Apr 15.
A 2-year-old intact male Asian Shepherd dog was referred with a history of chronic regurgitation along with normal appetite and diagnosis of megaesophagus on plain radiography. Clinical examination revealed normothermia, normocardia, normopnea, low body condition score and poor hair coat. The most important laboratory findings include anemia, azotemia, hyperlipidemia, increased thyroid stimulating hormone, decreased thyroxine and hypocortisolemia, as well as a marked increase in acetylcholine receptor antibody concentration. Based on the results, in addition to primary hypothyroidism and primary hypoadrenocorticism, myasthenia gravis was also diagnosed as an underlying cause of megaesophagus. Following nursing care and preferred treatment of each disease, the megaesophagus was resolved in the next visit. This clinical report describes for the first time, to the authors' knowledge, a dog with a rare type of autoimmune polyglandular syndrome (APS) known in human medicine as a Schmidt's syndrome. We want to emphasize the importance of clinicians' awareness regarding the possibility of APS to identify different diseases caused by it in order to achieve successful treatment.
一只2岁未绝育的雄性亚洲牧羊犬因慢性反流病史、食欲正常且在X线平片上诊断为巨食管症而前来就诊。临床检查发现体温正常、心率正常、呼吸正常、体况评分低且被毛状况不佳。最重要的实验室检查结果包括贫血、氮质血症、高脂血症、促甲状腺激素升高、甲状腺素降低、皮质醇血症以及乙酰胆碱受体抗体浓度显著升高。根据这些结果,除原发性甲状腺功能减退和原发性肾上腺皮质功能减退外,重症肌无力也被诊断为巨食管症的潜在病因。经过护理及对每种疾病的针对性治疗,下次复诊时巨食管症已得到缓解。据作者所知,本临床报告首次描述了一只患有罕见类型自身免疫性多腺体综合征(APS)的犬,在人类医学中这种综合征被称为施密特综合征。我们想强调临床医生认识到APS可能性的重要性,以便识别由其引起的不同疾病从而实现成功治疗。