Publicação
A VERY “FAMILIAR” HEART PAIN
| Resumo: | Introduction: Familial hypercholesterolemia (FH) is one of the most common autosomal-dominant genetic disorder, characterized by elevations of low-density lipoprotein cholesterol (LDL-C), constituting a major factor in the development and progression of premature atherosclerotic disease. Case Report: We describe the case of a 33-year-old female who attended the medical center with chief complaint of pressure-type chest pain, that lasted about 36 h, this radiating to the neck. The patient has been followed up at this medical center since 2021, with a personal medical history of dyslipidemia and primary infertility (in hospital follow-up). On physical examination, cardiac pain was suspected, this being the reason why the patient was referred to the hospital emergency department. As a result of this referral, the patient remained in the observation. Multiple complementary diagnostic tests were performed and due to the changes found in the Electrocardiogram (ECG) and in the high sensitivity troponin assay (hsTNI), the diagnosis of acute myocardial infarction without ST-segment elevation was assumed. Subsequently, the patient was transferred to the Cardiology Service where she underwent the analytical study, Echocardiogram and Coronarography. As result, was identified an subocclusion of the circumflex artery and an angioplasty with placement of a drug- stent was performed. At discharge, the diagnosis of familial hypercholesterolemia has been assumed and a few days later, the request for treatment of this patient with inhibitors Proprotein convertase subtilisin/kexin type 9 (iPCSK9) was approved. Our patient is already undergoing the prescribed therapy, while awaiting for genetic tests for the study of FH. Discussion: FH is an underdiagnosed and undertreated disease. Early recognition and institution of treatment substantially reduces the risk of premature atherosclerotic disease and major adverse cardiovascular events. Our case describes a FH that manifested as premature ischemic heart disease in a patient diagnosed with dyslipidemia, but without doing a specific treatment. |
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| Autores principais: | Ciubotaru, Victoria |
| Outros Autores: | Lourenço, Rita; Pinto, Luís |
| Assunto: | hipercolesterolemia familiar enfarte agudo de miocárdio diagnostico precoce Familial hypercholesterolemia acute myocardial infarction early diagnosis |
| Ano: | 2023 |
| País: | Portugal |
| Tipo de documento: | artigo |
| Tipo de acesso: | unknown |
| Instituição associada: | Sociedade Portuguesa de Hipertensão |
| Idioma: | português |
| Origem: | Revista Portuguesa de Hipertensão e Risco Cardiovascular |
| Resumo: | Introduction: Familial hypercholesterolemia (FH) is one of the most common autosomal-dominant genetic disorder, characterized by elevations of low-density lipoprotein cholesterol (LDL-C), constituting a major factor in the development and progression of premature atherosclerotic disease. Case Report: We describe the case of a 33-year-old female who attended the medical center with chief complaint of pressure-type chest pain, that lasted about 36 h, this radiating to the neck. The patient has been followed up at this medical center since 2021, with a personal medical history of dyslipidemia and primary infertility (in hospital follow-up). On physical examination, cardiac pain was suspected, this being the reason why the patient was referred to the hospital emergency department. As a result of this referral, the patient remained in the observation. Multiple complementary diagnostic tests were performed and due to the changes found in the Electrocardiogram (ECG) and in the high sensitivity troponin assay (hsTNI), the diagnosis of acute myocardial infarction without ST-segment elevation was assumed. Subsequently, the patient was transferred to the Cardiology Service where she underwent the analytical study, Echocardiogram and Coronarography. As result, was identified an subocclusion of the circumflex artery and an angioplasty with placement of a drug- stent was performed. At discharge, the diagnosis of familial hypercholesterolemia has been assumed and a few days later, the request for treatment of this patient with inhibitors Proprotein convertase subtilisin/kexin type 9 (iPCSK9) was approved. Our patient is already undergoing the prescribed therapy, while awaiting for genetic tests for the study of FH. Discussion: FH is an underdiagnosed and undertreated disease. Early recognition and institution of treatment substantially reduces the risk of premature atherosclerotic disease and major adverse cardiovascular events. Our case describes a FH that manifested as premature ischemic heart disease in a patient diagnosed with dyslipidemia, but without doing a specific treatment. |
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