Massive thymic hyperplasia in a toddler masquerading as a loculated pleural effusion: A case report
Pediatric massive thymic hyperplasia is a rare condition that can masquerade as a respiratory illness, making diagnosis challenging. An 18-month-old female with a 3-month history of multiple admissions for suspected pneumonia warranting antibiotics presented with recurrent respiratory distress, fevers, and fatigue. Work-up for possible parapneumonic effusion, including six chest x-rays and an ultrasound, eventually led to a computed tomography (CT) of the chest, which revealed a large homogeneous mass occupying much of the right-hemithorax. Percutaneous core biopsy showed thymocytes suggestive of either a massive thymic hyperplasia or a thymoma. Consensus was to proceed with upfront surgical resection of the mass, which was performed via right thoracotomy. Pathology was consistent with true thymic hyperplasia. The post-operative course was uncomplicated, and no issues were identified at 3-month follow-up. We plan to follow the patient at 6 months, 1 year, and then annually with surveillance chest x-rays to monitor for recurrence case-report. Thymic hyperplasia should be included in the differential diagnosis of pediatric patients with persistent respiratory symptoms and abnormal findings on chest x-ray.
Authors
- Michael G. Caty (ORCID: https://orcid.org/0000-0003-4883-0356)
- Matthew P. Shaughnessy (ORCID: https://orcid.org/0000-0002-2346-7784)
- Hao Wu (ORCID: https://orcid.org/0000-0001-6751-3036)
- Matthew A. Hornick (ORCID: https://orcid.org/0000-0001-8059-0028)
- Emily J. Zolfaghari
- Emily Christison-Lagay
Institutions
- Yale New Haven Hospital (US)
Publication Details
- Journal
- Journal of Pediatric Surgery Case Reports
- Published
- 2024-09-16
- DOI
- https://doi.org/10.1016/j.epsc.2024.102885
- Primary Topic
- Myasthenia Gravis and Thymoma
- Type
- article
- Field-Weighted Citation Impact
- 0.00