首页> 外文期刊>Internal medicine. >A Case of Juvenile Acromegaly that was Initially Diagnosed as Severe Congestive Heart Failure from Acromegaly-Induced Dilated Cardiomyopathy
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A Case of Juvenile Acromegaly that was Initially Diagnosed as Severe Congestive Heart Failure from Acromegaly-Induced Dilated Cardiomyopathy

机译:最初被诊断为由肢端肥大症引起的扩张型心肌病导致的严重充血性心力衰竭的一例青少年肢端肥大症

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摘要

Acromegaly is characterized by chronic hypersecretion of growth hormone (GH) and is associated with increased mortality rate because of the potential complications such as cardiovascular disease, respiratory disease, or malignancy, which are probably caused by the long-term exposure of tissues to excess GH, for at least 10 years, before diagnosis and treatment.A 22-year-old man with a 2-month history of fatigue was admitted to our hospital because of chest discomfort, dyspnea, and pitting edema of the lower limbs experienced over a 1-month period. On admission, his height and body weight were 186 cm and 138.5 kg, respectively, with a BMI of 39.8 kg/m2. He showed acromegalic features and elevated serum GH and IGF-1 levels, which were 11.5 ng/mL and 960 ng/mL, respectively. There was no GH suppression in the 75-g oral glucose tolerance test. Pituitary magnetic resonance imaging (MRI) revealed microadenoma. Chest X-ray revealed cardiomegaly, and echocardiogram showed dilated left ventricular (LV) cavity and diffuse hypokinesis with extremely decreased ejection fraction (EF). He was diagnosed as having acromegaly with congestive heart failure from diastolic cardiomyopathy.After the successful transsphenoidal resection of the pituitary adenoma, the level of GH was normalized. However, the cardiac dysfunction did not show any improvement even after the administration of β-blockers, angiotensin-converting enzyme inhibitor (ACE-I), or diuretics. The patient was re-hospitalized, and he died of cardiac failure at the age of 25 years.Patients with acromegaly have been reported to have about 30% higher mortality rate, and cardiovascular disease accounts for 60% of the deaths. We report a case of a patient with juvenile acromegaly who was diagnosed with severe cardiac failure at the time of diagnosis and failed to recover cardiac function even after the successful resection of the pituitary adenoma. Immediate diagnosis and treatment are required for better control of acromega...
机译:肢端肥大症的特征在于生长激素(GH)的慢性过度分泌,并且由于诸如心血管疾病,呼吸系统疾病或恶性肿瘤的潜在并发症而导致死亡率增加,这可能是由于组织长期暴露于过量的GH引起的在诊断和治疗之前至少持续了10年。一名22个月的疲劳病史为2个月的男性因胸部不适,呼吸困难和下肢点状浮肿而入院,住院时间超过1岁。月期间。入院时,他的身高和体重分别为186 cm和138.5 kg,BMI为39.8 kg / m2。他表现出肢端肥大症特征,血清GH和IGF-1水平升高,分别为11.5 ng / mL和960 ng / mL。口服75克葡萄糖耐量试验未发现GH抑制。垂体磁共振成像(MRI)显示微腺瘤。胸部X光检查显示心脏肥大,超声心动图显示左心室(LV)腔扩张和运动功能减退,射血分数(EF)大大降低。他被诊断为患有舒张性心肌病的充血性心力衰竭伴肢端肥大症。成功经蝶窦切除垂体腺瘤后,GH水平恢复正常。然而,即使在使用β-阻滞剂,血管紧张素转化酶抑制剂(ACE-1)或利尿剂后,心脏功能障碍也未见任何改善。该患者再次住院治疗,死于心力衰竭,享年25岁。据报道,肢端肥大症患者的死亡率高约30%,心血管疾病占死亡人数的60%。我们报告一例少年肢端肥大症患者,在诊断时被诊断出患有严重的心力衰竭,即使成功切除了垂体腺瘤也未能恢复心脏功能。为了更好地控制肢端肥大症,需要立即诊断和治疗。

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