Acromegaly in a domestic short-haired cat: first report from Iran.

M. Rezaei, M. Saberi, A. Shafiian, M. Zamani-Ahmadmahmudi
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Abstract

Acromegaly, a syndrome characterized by overgrowth of bony and soft tissue, is caused following chronic excessive production of growth hormone (GH)[1]. It is a well-recognized but rare condition in cats caused by a functional somatotroph adenoma in the anterior pituitary gland[2,3]. This disorder is encountered most often in middle-aged and elderly, predominantly male, cats[1]. Catabolic and diabetogenic effects of GH, the anabolic effects of IGF-1 and the space-occupying effect of the pituitary adenoma are responsible for clinical signs[4]. The physical changes in cats tend to be less pronounced than in dogs. Increased body size, especially large head and abdominal enlargement are prominent. Affected cats may have respiratory signs, which is due to soft tissue thickening in the pharyngeal region and consequent extrathoracic upper airway obstruction. Moreover, hypertrophic cardiomyopathy is another cause of dyspnea in these cases. Neurological signs resulting from large pituitary adenoma may also manifest[3,5]. In advanced cases, clinical manifestation may include prominent facial features, generalized bone/soft tissue enlargement, and prognathia[5]. An association between pituitary adenoma and diabetes mellitus (DM) was well described in cats[6]. More recently, feline acromegaly has been reported in several cats with concurrent insulin-resistant DM[7,8]. A GH-induced postreceptor defect in insulin action at the level of target tissues is believed to be the cause of concurrent diabetes in most cats with acromegaly[2]. Acromegaly is mainly diagnosed based upon increased serum GH concentration[9]. Computed tomography (CT) or magnetic resonance (MR) imaging of the head is also recommended to confirm the presence of a pituitary tumor[10]. Radiation therapy has been reported as the most effective treatment for feline acromegaly. It leads to improved neurologic signs and decreased insulin requirements[3,5]. This study is the first case report of a diabetic cat with acromegaly in Iran, which described historic and clinical signs and laboratory findings associated with the condition.
一只家养短毛猫的肢端肥大症:首次来自伊朗的报告。
肢端肥大症是一种以骨和软组织过度生长为特征的综合征,由生长激素(GH)的长期过量产生引起[1]。这是一种公认但罕见的猫疾病,由垂体前叶的功能性生长激素腺瘤引起[2,3]。这种疾病最常见于中老年猫,主要是雄性猫[1]。GH的分解代谢和糖尿病作用、IGF-1的合成代谢作用和垂体腺瘤的占位作用是临床症状的原因[4]。猫的身体变化往往不如狗明显。体型增大,尤其是大头和腹部增大是突出的。受影响的猫可能会出现呼吸体征,这是由于咽部软组织增厚和随之而来的胸外上呼吸道阻塞。此外,肥厚性心肌病是这些病例呼吸困难的另一个原因。大垂体腺瘤引起的神经系统体征也可能表现出来[3,5]。在晚期病例中,临床表现可能包括突出的面部特征、全身骨/软组织肿大和前颌[5]。垂体腺瘤与糖尿病(DM)之间的关联在猫身上得到了很好的描述[6]。最近,据报道,几只同时患有胰岛素抵抗型糖尿病的猫出现了肢端肥大症[7,8]。GH诱导的受体后胰岛素作用在靶组织水平上的缺陷被认为是大多数肢端肥大症猫并发糖尿病的原因[2]。肢端肥大症的诊断主要基于血清GH浓度的升高[9]。还建议对头部进行计算机断层扫描(CT)或磁共振(MR)成像,以确认垂体瘤的存在[10]。据报道,放射治疗是治疗猫肢端肥大症最有效的方法。它可改善神经系统症状并降低胰岛素需求[3,5]。这项研究是伊朗首例糖尿病猫肢端肥大症病例报告,描述了与该疾病相关的历史和临床体征以及实验室发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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