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Turk Pediatri Ars. 2019 Dec 25;54(4):267-271. doi: 10.14744/TurkPediatriArs.2018.05668. eCollection 2019.

Abdominal pain in a patient with sickle cell disease with multiple complications.

Author information

1
Health Research Institute, Non-Communicable Pediatric Diseases Research Center, Babol, Iran.

Abstract

in English, Turkish

Sickle cell disease is an inherited autosomal recessive hemoglobinopathy. Acute abdominal pain is the cause of hospitalization in 10% of patients with sickle cell disease and usually occurs during vaso-occlusion or distal tissue ischemia. Determining the etiology of abdominal pain is very difficult in these patients because it is associated with several rare diagnoses, such as pancreatitis and splenic abscess in some patients. We represent a 14-year-old boy with sickle cell disease who was hospitalized due to acute abdominal pain and indicated multiple and scarce disturbances in the spleen and hepatobiliary system.

KEYWORDS:

Abdominal pain; cholelithiasis; pancreatitis; sickle cell disease; splenic abscess

Conflict of interest statement

Conflict of Interest: No conflict of interest was declared by the authors.

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