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.

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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
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article

Massive thymic hyperplasia in a toddler masquerading as a loculated pleural effusion: A case report

Michael G. Caty, Matthew P. Shaughnessy, Hao Wu, Matthew A. Hornick et al.
Journal of Pediatric Surgery Case Reports
Myasthenia Gravis and Thymoma
article

Massive thymic hyperplasia in a toddler masquerading as a loculated pleural effusion: A case report

Michael G. Caty, Matthew P. Shaughnessy, Hao Wu, Matthew A. Hornick, Emily J. Zolfaghari, Emily Christison-Lagay
article en

Abstract

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.

Journal of Pediatric Surgery Case ReportsVol. 110
Yale New Haven Hospital (US)
Zero hunger
Openalex Percentile: Top 75%
Myasthenia Gravis and Thymoma
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Massive thymic hyperplasia in a toddler masquerading as a loculated pleural effusion: A case report — Michael G. Caty, Matthew P. Shaughnessy, et al. · Journal of Pediatric Surgery Case Reports (2024) | TGRS Research Map | TGRS