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Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
Published on: February 17, 2022
NEUROENDOCRINE TUMOR IN A CHILD WITH COMMON VARIABLE IMMUNODEFICIENCY
Pedro de Souza Lucarelli Antunes1, Heloísa Gabriel Tersariol1, Mainã Marques Belém Veiga1
1School of Medical Sciences, Santa Casa de São Paulo, São Paulo, SP, Brazil.
A child with Common Variable Immunodeficiency developed digestive symptoms and a neuroendocrine tumor. This case highlights the need to investigate digestive neoplasms in children with this immunodeficiency for better outcomes.
Area of Science:
- Pediatric Immunology
- Gastroenterology
- Oncology
Background:
- Common Variable Immunodeficiency (CVID) is a primary immunodeficiency characterized by hypogammaglobulinemia.
- Adults with CVID have an increased risk of gastric tumors.
- The association between CVID and neuroendocrine tumors in children is not well-established.
Observation:
- A pediatric case of CVID presented with recurrent pneumonias from one year of age.
- At eight years, the patient developed epigastric pain, progressing to chronic diarrhea and weight loss by age ten.
- A neuroendocrine tumor was diagnosed, leading to rapid disease progression.
Findings:
- This is the first reported case of a neuroendocrine tumor in a pediatric patient with Common Variable Immunodeficiency.
- The patient's gastrointestinal symptoms were indicative of a developing neoplasm.
- The tumor exhibited rapid progression despite treatment.
Implications:
- Early investigation for digestive neoplasms should be considered in pediatric patients with CVID presenting with gastrointestinal symptoms.
- Recognizing this association may improve diagnostic timelines and patient prognosis.
- Further research is needed to understand the link between CVID and neuroendocrine tumors in children.
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