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Follicular lymphoid hyperplasia simulating intussusception in a 6-year-old boy: clinical, radiological and
Ludger W Poll1, Gerd-M Lackmann, Philip May
1Institute of Diagnostic Radiology, Section of Pediatric Radiology, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany. polll@uni-duesseldorf.de
Insights
Follicular lymphoid hyperplasia can mimic intussusception in children, presenting as abdominal pain and enlarged lymph nodes. This condition requires consideration in differential diagnoses for suspected intussusception without significant symptoms.
Area of Science:
- Pediatric Surgery
- Gastroenterology
- Pediatric Radiology
Background:
- Recurrent abdominal pain in children can stem from various causes, including intussusception.
- Diagnostic imaging like ultrasound and CT are crucial for identifying intussusception.
- Abdominal lymphadenopathy can be associated with intussusception.
Observation:
- A 6-year-old boy presented with recurrent abdominal pain and imaging findings suggestive of ileocecal intussusception.
- The suspected intussusception showed no morphological changes over a 4-week follow-up.
- Surgery revealed a cecal tumor instead of intussusception.
Findings:
- Histopathology after resection confirmed follicular lymphoid hyperplasia, not intussusception.
- Follicular lymphoid hyperplasia can radiologically mimic intussusception in children.
- This diagnosis was made in a case initially suspected to be a tumor or lymphoma.
Implications:
- Follicular lymphoid hyperplasia should be considered in the differential diagnosis of pediatric intussusception, especially with subtle or absent symptoms.
- Radiologists and surgeons should be aware of this mimicker to avoid unnecessary surgical interventions.
- Accurate diagnosis through histopathology is essential for appropriate management in pediatric abdominal masses.
Abstract:
We report the case of a 6-year-old boy who initially presented with recurrent abdominal pain. Diagnostic imaging, including ultrasound and CT, showed findings typical of an ileocecal intussusception with abdominal lymphadenopathy. Sonographically, the morphological appearance of the intussusception did not change during a 4-week follow-up period. Surgery was performed on the tentative diagnosis of a tumour versus lymphoma. Upon laparatomy, intussusception was ruled out and a large, broad-based tumour of the caecum was palpable. The histopathology after ileocecal resection revealed follicular lymphoid hyperplasia. Where there is radiological suspicion of an intussusception in children with no or insignificant symptoms, follicular lymphoid hyperplasia should be included in the differential diagnosis.
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