Greco D S, Peterson M E, Cho D Y, Markovits J E
J Am Vet Med Assoc. 1985 Nov 1;187(9):948-50.
Juvenile-onset hypothyroidism was diagnosed in an adult mixed-breed dog examined because of quadraparesis. Unusual clinical signs attributable to juvenile-onset or congenital hypothyroidism included disproportionate dwarfism; enlarged, protruding tongue; mental dullness; and retention of a "puppy" coat, which was soft and fluffy, without guard hairs. Radiography of the vertebral column and long bones revealed multiple areas of delayed epiphyseal closure and epiphyseal dysgenesis. Myelography demonstrated several intervertebral disk protrusions in the cervical and lumbar regions. Hypothyroidism was confirmed on the basis of a low basal serum thyroxine concentration that failed to increase after the administration of thyroid stimulating hormone. Other laboratory abnormalities included nonregenerative, normocytic, normochromic anemia; mild hypercalcemia; and an impaired growth hormone (GH) secretory response after xylazine administration. At necropsy, the thyroid gland was small and weighed only 0.2g. Microscopic examination of the thyroid gland revealed a loss of glandular tissue, which was replaced by adipose tissue along its periphery. Gross or microscopic abnormalities were not noted in the pituitary gland, and immunohistochemical staining of the pituitary gland revealed a normal number of GH-containing acidophils. This suggests that primary hypothyroidism may result in an impaired secretion of growth hormone, and that pituitary dwarfism or GH deficiency may be difficult to differentiate from hypothyroid dwarfism on the basis of provocative GH testing alone.
一只成年混血犬因四肢轻瘫接受检查,被诊断为幼年型甲状腺功能减退症。幼年型或先天性甲状腺功能减退症的不寻常临床症状包括不成比例的侏儒症、舌头肿大突出、精神迟钝以及保留柔软蓬松的“幼犬”被毛,没有针毛。脊柱和长骨的X线摄影显示多个骨骺闭合延迟和骨骺发育异常区域。脊髓造影显示颈椎和腰椎区域有多处椎间盘突出。根据基础血清甲状腺素浓度低且在注射促甲状腺激素后未升高,确诊为甲状腺功能减退症。其他实验室异常包括非再生性、正细胞正色素性贫血、轻度高钙血症以及注射赛拉嗪后生长激素(GH)分泌反应受损。尸检时,甲状腺很小,仅重0.2克。甲状腺的显微镜检查显示腺组织丧失,其周边被脂肪组织取代。垂体未发现大体或显微镜下异常,垂体的免疫组织化学染色显示含生长激素嗜酸细胞数量正常。这表明原发性甲状腺功能减退症可能导致生长激素分泌受损,并且仅根据激发性GH检测很难将垂体性侏儒症或GH缺乏症与甲状腺功能减退性侏儒症区分开来。