Corsini Andrea, Bianchi Ezio, Volta Antonella, Bonazzi Mattia
Department of Veterinary Science, University of Parma, Parma, Italy.
JFMS Open Rep. 2020 Feb 20;6(1):2055116920906936. doi: 10.1177/2055116920906936. eCollection 2020 Jan-Jun.
A 17-year-old neutered male European Shorthair cat was presented owing to an inability to jump and respiratory stridor. The owner did not report any other clinical signs. On physical examination, the main findings were plantigrade stance, broad facial features and inspiratory stridor. Neurological examination revealed posterior paraparesis, hypotonia and right hindlimb muscle atrophy. Laboratory findings were unremarkable and glycaemia was normal. Serum insulin-like growth factor 1 concentration was elevated (>1000 ng/ml). A total body CT scan showed an enlarged pituitary gland, thickening of the nasal turbinates and an L7-S1 right foraminal stenosis. Electrodiagnostic testing confirmed the presence of a neuropathy affecting both sciatic nerves. The cat was treated with gabapentin only and was still alive and euglycaemic 16 months after the diagnosis.
This case describes for the first time sciatic neuropathy, an occasional complication of acromegaly in people, as a possible clinical presentation in acromegalic cats without concurrent diabetes mellitus.
一只17岁已绝育的雄性欧洲短毛猫因无法跳跃和呼吸喘鸣前来就诊。主人未报告其他任何临床症状。体格检查时,主要发现为跖行姿势、面部特征宽阔和吸气性喘鸣。神经学检查显示后肢轻瘫、肌张力减退和右后肢肌肉萎缩。实验室检查结果无异常,血糖正常。血清胰岛素样生长因子1浓度升高(>1000 ng/ml)。全身CT扫描显示垂体增大、鼻甲增厚和L7 - S1右侧椎间孔狭窄。电诊断测试证实存在影响双侧坐骨神经的神经病变。该猫仅接受加巴喷丁治疗,诊断后16个月仍存活且血糖正常。
本病例首次描述了坐骨神经病变,这是人类肢端肥大症的一种偶发并发症,在无并发糖尿病的肢端肥大症猫中可能作为一种临床表现。