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Organizing Pneumonia: A Clinical Challenge in a Child With Previous Rhabdomyosarcoma
Ricardo Barreto Mota1, Diogo Costa Carvalho1, Inês Azevedo1,2
1Centro Hospitalar Universitário de São João, Porto, Portugal.
Insights
Organizing pneumonia is a rare lung disease. This case highlights its potential occurrence in adolescents with a history of rhabdomyosarcoma, emphasizing diagnostic considerations.
Area of Science:
- Pulmonology
- Pediatric Oncology
- Radiology
Background:
- Organizing pneumonia is a rare pulmonary disease with an unknown cause, infrequently reported in children.
- It can arise secondary to treatments like chemotherapy, radiation therapy, or hematopoietic cell transplantation.
Observation:
- An 18-year-old male presented with respiratory symptoms 8 years post-treatment for rhabdomyosarcoma.
- Imaging revealed nodular opacities and ground-glass opacities in the lungs, with one cavitated lesion.
Findings:
- Microbiological work-up, including tuberculosis screening, was negative.
- A biopsy confirmed findings suggestive of organizing pneumonia.
- The patient experienced spontaneous resolution of symptoms.
Implications:
- This case underscores the importance of considering organizing pneumonia in patients with pulmonary lesions and a history of specific treatments (e.g., stem cell transplant, lung irradiation, immunosuppression).
- Pulmonary metastases and secondary tumors should be differential diagnoses in patients with relapsed rhabdomyosarcoma.
- The diagnostic challenge presented by this rare condition in a pediatric oncology patient is highlighted.
Abstract:
Organizing pneumonia is a pulmonary disease of undefined etiology, with few reported cases in children. It may be secondary to chemotherapy, radiation therapy, infectious agents, or hematopoietic cell transplantation. We present a case of an 18-year-old boy who presented to a follow-up consult with respiratory symptoms at the age of 11 years, 8 years after finishing treatment for a prostatic relapse of a pelvic rhabdomyosarcoma. Chest radiography revealed nodular opacities in the left lung, the one in the left lower lobe with silhouette sign with the left hemidiaphragm. Chest computerized tomography showed 2 nodular lesions in the left upper lobe, one of them cavitated, and another nodular lesion in the left lower lobe; 2 of these nodules had surrounding ground-glass opacities. Microbiological work-up, including tuberculosis screening, was negative. Biopsy revealed findings suggestive of organizing pneumonia. He presented spontaneous resolution. This case presented a diagnostic challenge due to rarity of this condition and its indetermined association with the patient's history of rhabdomyosarcoma. With this case, the authors alert that organizing pneumonia must be considered in patients presenting with pulmonary lesions with a history of previous hematopoietic stem cell transplants, lung irradiation, or immunosuppression. Pulmonary metastases and secondary tumors must be considered as a differential diagnosis in patients with a heavily treated relapsed rhabdomyosarcoma.
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