Peterson M E, Kintzer P P, Kass P H
Department of Medicine, Animal Medical Center, New York, NY 10021, USA.
J Am Vet Med Assoc. 1996 Jan 1;208(1):85-91.
To evaluate clinical and laboratory findings in 225 dogs with naturally occurring hypoadrenocorticism diagnosed over a 14-year period.
Retrospective case series.
220 dogs with primary hypoadrenocorticism and 5 dogs with secondary hypoadrenocorticism (primary ACTH deficiency).
We reviewed medical records of all dogs with naturally occurring hypoadrenocorticism examined at The Animal Medical Center between 1979 and 1993 or at Tufts University, Foster Hospital for Small Animals, between 1987 and 1993.
Dogs ranged from 4 months to 14 years old. Most (71%) were female, and female dogs had a significantly higher relative risk of developing hypoadrenocorticism than did males. Great Danes, Portuguese Water Dogs, Rottweilers, Standard Poodles, West Highland White Terriers, and Wheaton Terriers had a significantly higher relative risk of developing hypoadrenocorticism than did dogs of other breeds. Common owner complaints included lethargy, poor appetite, and vomiting, whereas lethargy, weakness, and dehydration were common abnormalities detected on physical examination. Serum biochemical testing at the time of diagnosis revealed moderate-to-severe azotemia and hyperphosphatemia in most dogs. In 99 of 172 (57.6%) dogs that had a pretreatment urinalysis performed, urine specific gravity was < 1.030 even though dogs were azotemic. Serum electrolyte changes included hyperkalemia (n = 215), hyponatremia (183), hypochloremia (94), and hypercalcemia (69). Five of the 220 dogs with primary hypoadrenocorticism and the 5 dogs with secondary hypoadrenocorticism did not have hyperkalemia at time of diagnosis. In all dogs, ACTH stimulation testing revealed a low to low-normal baseline serum cortisol concentration with little to no rise after ACTH administration. Endogenous plasma ACTH concentration measured in 35 dogs with primary hypoadrenocorticism was markedly high; whereas ACTH concentration was undetectable to low in the 5 dogs with secondary hypoadrenocorticism.
hypoadrenocorticism is a rare disease in dogs, most commonly affecting young to middle-aged females; some breeds are at greater risk of developing the disease than others. In general, clinical signs are nonspecific and similar to manifestations of more common diseases. Serum electrolyte disturbances of hyperkalemia and hypernatremia are characteristic in dogs with primary hypoadrenocorticism, but concentrations may be normal in dogs with early or mild primary or secondary hypoadrenocorticism. Diagnosis of hypoadrenocorticism is best confirmed by demonstration of a low baseline serum cortisol concentration with a subnormal or negligible response to ACTH administration. Determination of endogenous plasma ACTH concentrations is valuable in differentiating primary from secondary hypoadrenocorticism, particularly in dogs with normal serum electrolyte concentrations.
评估在14年期间确诊的225只患有自然发生的肾上腺皮质功能减退症的犬的临床和实验室检查结果。
回顾性病例系列研究。
220只原发性肾上腺皮质功能减退症犬和5只继发性肾上腺皮质功能减退症犬(原发性促肾上腺皮质激素缺乏)。
我们回顾了1979年至1993年在动物医疗中心或1987年至1993年在塔夫茨大学福斯特小动物医院检查的所有患有自然发生的肾上腺皮质功能减退症犬的病历。
犬的年龄范围为4个月至14岁。大多数(71%)为雌性,雌性犬患肾上腺皮质功能减退症的相对风险显著高于雄性犬。大丹犬、葡萄牙水犬、罗威纳犬、标准贵宾犬、西部高地白梗和惠比特梗患肾上腺皮质功能减退症的相对风险显著高于其他品种的犬。主人常见的主诉包括嗜睡、食欲不振和呕吐,而嗜睡、虚弱和脱水是体格检查中常见的异常表现。诊断时的血清生化检测显示大多数犬有中度至重度氮质血症和高磷血症。在172只进行了治疗前尿液分析的犬中,有99只(57.6%)即使处于氮质血症状态,尿比重仍<1.030。血清电解质变化包括高钾血症(n = 215)、低钠血症(183)、低氯血症(94)和高钙血症(69)。220只原发性肾上腺皮质功能减退症犬中的5只和5只继发性肾上腺皮质功能减退症犬在诊断时没有高钾血症。在所有犬中,促肾上腺皮质激素刺激试验显示基线血清皮质醇浓度低至低正常,给予促肾上腺皮质激素后几乎没有升高。在35只原发性肾上腺皮质功能减退症犬中测得的内源性血浆促肾上腺皮质激素浓度明显升高;而在5只继发性肾上腺皮质功能减退症犬中,促肾上腺皮质激素浓度检测不到或很低。
肾上腺皮质功能减退症在犬中是一种罕见疾病,最常见于年轻至中年雌性;某些品种比其他品种患该病的风险更高。一般来说,临床症状不具特异性,与更常见疾病的表现相似。原发性肾上腺皮质功能减退症犬的特征性血清电解质紊乱为高钾血症和高钠血症,但早期或轻度原发性或继发性肾上腺皮质功能减退症犬的浓度可能正常。肾上腺皮质功能减退症的诊断最好通过证明基线血清皮质醇浓度低且对促肾上腺皮质激素给药反应低于正常或可忽略不计来确诊。测定内源性血浆促肾上腺皮质激素浓度对于区分原发性和继发性肾上腺皮质功能减退症很有价值,特别是对于血清电解质浓度正常的犬。