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Published on: July 29, 2012
Advanced megaesophagus (Group III) secondary to vector-borne Chagas disease in a 20-month-old infant
Anis Rassi1, Joffre Marcondes de Rezende, Anis Rassi
1Faculdade de Medicina, Universidade Federal de Goiás, Goiânia, GO.
Insights
Chagas disease in an infant caused megaesophagus and malnutrition, successfully treated with surgery and benznidazole. Long-term follow-up showed no disease recurrence and normal development, including a healthy pregnancy.
Area of Science:
- Infectious Diseases
- Pediatric Gastroenterology
- Tropical Medicine
Background:
- Chagas disease, caused by *Trypanosoma cruzi*, can lead to chronic complications like megaesophagus.
- Megaesophagus in infants presents significant challenges, including severe malnutrition and feeding difficulties.
Observation:
- A female infant presented with Group III megaesophagus attributed to congenital Chagas disease.
- The infant experienced severe malnutrition, necessitating surgical intervention (Heller technique).
Findings:
- Post-surgery, the patient received benznidazole, leading to parasitological and serological cure of Chagas disease.
- Long-term follow-up over several years demonstrated sustained disease remission, normal physical development, and a healthy pregnancy at age 23.
- Thirty years post-diagnosis, the patient maintained normal cardiac and pulmonary function, evidenced by normal electrocardiogram, echocardiogram, and chest radiography.
Implications:
- This case highlights the successful management of pediatric megaesophagus secondary to Chagas disease.
- It underscores the importance of early diagnosis and treatment of Chagas disease in preventing long-term morbidity.
- The findings support the efficacy of combined surgical and antiparasitic treatment for severe congenital Chagas disease with esophageal involvement.
Abstract:
The authors report the case of a female infant with Group III (or Grade III) megaesophagus secondary to vector-borne Chagas disease, resulting in severe malnutrition that reversed after surgery (Heller technique). The infant was then treated with the antiparasitic drug benznidazole, and the infection was cured, as demonstrated serologically and parasitologically. After follow-up of several years without evidence of disease, with satisfactory weight and height development, the patient had her first child at age 23, in whom serological tests for Chagas disease yielded negative results. Thirty years after the initial examination, the patient's electrocardiogram, echocardiogram, and chest radiography remained normal.
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