Unusual cause of abdominal pain and jaundice in emergency: case report

We analyzed a young man with a history of jaundice since childhood and cholelithiasis, who presented with abdominal pain, jaundice, and splenomegaly. Initially, a diagnosis of dengue was considered, because of the prevalence of this disease in the patient's geographic region. However, additional testing identified hereditary spherocytosis, a genetic hemolytic disorder. The importance of considering alternative diagnoses in the face of common symptoms in emergencies is emphasized. Initial dengue-oriented management was followed by targeted treatment for hereditary spherocytosis after the diagnosis was confirmed. The result was a significant improvement in the patient. This case emphasizes the need for thorough anamnesis and meticulous diagnostic evaluation to prevent diagnostic errors and inappropriate treatment, highlighting how inherited diseases can mimic infectious conditions in complex clinical scenarios.

Authors

Publication Details

Journal
Revista de la Facultad de Medicina Humana
Published
2024-10-31
DOI
https://doi.org/10.25176/rfmh.v24i4.6531
Primary Topic
Pediatric Hepatobiliary Diseases and Treatments
Type
article
Field-Weighted Citation Impact
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article

Unusual cause of abdominal pain and jaundice in emergency: case report

Loyda Miranda-Chávez, Jessica Calcino, Ricardo Ayala
Revista de la Facultad de Medicina Humana
Pediatric Hepatobiliary Diseases and Treatments
article

Unusual cause of abdominal pain and jaundice in emergency: case report

Loyda Miranda-Chávez, Jessica Calcino, Ricardo Ayala
article en

Abstract

We analyzed a young man with a history of jaundice since childhood and cholelithiasis, who presented with abdominal pain, jaundice, and splenomegaly. Initially, a diagnosis of dengue was considered, because of the prevalence of this disease in the patient's geographic region. However, additional testing identified hereditary spherocytosis, a genetic hemolytic disorder. The importance of considering alternative diagnoses in the face of common symptoms in emergencies is emphasized. Initial dengue-oriented management was followed by targeted treatment for hereditary spherocytosis after the diagnosis was confirmed. The result was a significant improvement in the patient. This case emphasizes the need for thorough anamnesis and meticulous diagnostic evaluation to prevent diagnostic errors and inappropriate treatment, highlighting how inherited diseases can mimic infectious conditions in complex clinical scenarios.

Revista de la Facultad de Medicina HumanaVol. 24(4)
Good health and well-being
Openalex Percentile: Top 61%
Pediatric Hepatobiliary Diseases and Treatments
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