Author/Authors :
Jesse Durrance, Richard Department of Internal Medicine - Jamaica Hospital Medical Center, Jamaica, USA , Ullah, Tofura Department of Internal Medicine - Jamaica Hospital Medical Center, Jamaica, USA , Atif, Zulekha Department of Internal Medicine - Jamaica Hospital Medical Center, Jamaica, USA , Frumkin, William Department of Cardiology - Jamaica Hospital Medical Center, Jamaica, USA , Doshi, Kaushik Department of Internal Medicine - Jamaica Hospital Medical Center, Jamaica, USA
Abstract :
Chagas cardiomyopathy (CCM) is traditionally considered a disease restricted to areas of endemicity. However, an estimated
300,000 people living in the United States today have CCM, of which its majority is undiagnosed.We present a case of CCM acquired
in an endemic area and detected in its early stage. A 42-year-old El Salvadoran woman presented with recurrent chest pain and
syncopal episodes. Significant family history includes a sister in El Salvador who also began suffering similar episodes. Physical exam
and ancillary studies were only remarkable for sinus bradycardia. The patient was diagnosed with symptomatic sinus bradycardia
and a pacemaker was placed. During her hospital course, Chagas serology was ordered given the epidemiological context from
which she came. With no other identifiable cause, CCM was the suspected etiology. This case highlights the underrecognized
presence of Chagas in the United States and the economic and public health importance of its consideration in the etiological
differential diagnosis of electrocardiographic changes among Latin American immigrants. While the United States is not considered
an endemic area for Chagas disease, the influx of Latin American immigrants has created a new challenge to identify at-risk
populations, diagnose suspected cases, and provide adequate treatment for this disease.