Outcome of a pregnant woman with polymorbiditys: Case report

• Autor(a) principal: de Sousa Henriques, Anne Dryelle
• Data de Publicação: 2018
• Outros Autores: Miranda, Tallyta, de Sousa Sá, Suzane Maria, Ferreira Pessoa Oliveira, Kassandra
• Tipo de documento: Artigo
• Idioma: por
• Título da fonte: Anais da Faculdade de Medicina de Olinda (Online)
• Texto Completo: https://afmo.emnuvens.com.br/afmo/article/view/33
• topic: Gestação; Metilenotetrahidrofolato redutase; Hipotireoidismo; Gestation; Methylenetetrahydrofolate reductase; Hypothyroidism

Objective: To report the outcome of pregnant women with hypothyroidism and methylenethohydrofolate reductase mutation (MTHFR) indicative of hereditary thrombophilia trait. Case report: WSR, 38 year-old, puerperal, G1P1A0 and with a history of pulmonary thromboembolism (PTE) a year ago. The exams diagnosed hypothyroidism and trait heterozygous hereditary thrombophilia. She also had extreme fatigue due to a diagnosis of anemia, a low insertion placenta and lactose intolerance. At 35 weeks, emergency cesarean section, without intercurrences with the fetus. Comments: It is understood the importance of prenatal consultations in an active search for morbidities that may cause intercurrences for pregnant women and the fetus, in addition to multidisciplinary follow-up to provide the outcome favorable to gestation.