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
{"title":"Young female with acromegaloid features and pituitary macroadenoma: what is your diagnosis?","authors":"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","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":75610,"journal":{"name":"Boletin de la Asociacion Medica de Puerto Rico","volume":"106 1","pages":"49-53"},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Boletin de la Asociacion Medica de Puerto Rico","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.