Young female with acromegaloid features and pituitary macroadenoma: what is your diagnosis?

José Hernán Martínez, Carlos Figueroa-Núñez, Paola Mansilla-Letelier, Coromoto Palermo-Garofalo, Mónica Santiago, Oberto Torres, Rafael Trinidad, Michelle Mangual-García, Alfredo Sánchez, Madelin Gutierrez, María de Lourdes Miranda, Eva González
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Abstract

Pseudoacromegaly is a extremely rare condition previously described and characterized by acromegaloid changes, tissue overgrowth, without elevations in insulin-like growth factor or growth hormone as seen in Acromegaly. We present the case of a young female seen initially with acromegaloid features and a pituitary microadenoma. After work-up the patient was diagnosed as insulin-mediated pseudoacromegaly. Only a few cases of pseudoacromegaly has been reported and should always be considered when evaluating patients for acromegaloid features with negative biochemical and hormonal levels.

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年轻女性肢端肥大样特征和垂体大腺瘤:你的诊断是什么?
假性肢端肥大症是一种极其罕见的疾病,其特征是肢端肥大样细胞改变,组织过度生长,没有胰岛素样生长因子或生长激素升高,如肢端肥大症。我们提出的情况下,年轻的女性最初看到与肢端巨体特征和垂体微腺瘤。检查后诊断为胰岛素介导的假性肢端肥大症。只有少数假性肢端肥大症的病例被报道,在评估患者肢端肥大症的生化和激素水平阴性时,应始终考虑到这一点。
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