Unique presentation of late-onset Pneumocystis pneumonia in a pediatric kidney transplant recipient.


Journal

Pediatric transplantation
ISSN: 1399-3046
Titre abrégé: Pediatr Transplant
Pays: Denmark
ID NLM: 9802574

Informations de publication

Date de publication:
09 2023
Historique:
revised: 05 05 2023
received: 19 09 2022
accepted: 03 07 2023
medline: 28 8 2023
pubmed: 14 7 2023
entrez: 14 7 2023
Statut: ppublish

Résumé

Restrictive lung disease leading to abnormal lung function in kidney transplant recipients is commonly associated with noninfectious complications or medications used for post-transplant immunosuppression. Herein, we report an interesting case of pediatric kidney transplant recipient with weight loss and abnormal spirometry who was diagnosed to have late-onset Pneumocystis pneumonia. A 17-year-old male patient with a history of allergic rhinitis, mild persistent asthma, and deceased donor kidney transplant, performed 18 months prior, presented for routine evaluation of his asthma to the pulmonology clinic. He was clinically asymptomatic except for a weight loss of 8 kg over 6-month period prior to presentation. Patient's spirometry was suggestive of a restrictive pattern and further investigation using a high-resolution computed tomography (HRCT) of the chest showed bilateral diffuse ground-glass reticulonodular opacities with subpleural sparing suggestive of interstitial pneumonitis. A bronchoscopy with bronchoalveolar lavage revealed organisms consistent with Pneumocystis jirovecii on gomori-methenamine-silver (GMS) staining. Beta-d-glucan testing in serum revealed a level of >500 pg/mL (normal 0-59 pg/mL) further supportive of Pneumocystis jirovecii infection. Patient was treated with a 6-week course of trimethoprim-sulfamethoxazole. His weight loss and beta-d-glucan levels improved over a course of 6 months, and he continues to be on trimethoprim-sulfamethoxazole prophylaxis. Late-onset Pneumocystis jirovecii infection in kidney transplant recipients can have an atypical presentation. Treating physicians should consider PJP in the differential diagnosis of unexplained weight loss in pediatric kidney transplant recipients, especially those receiving a large cumulative burden of immunosuppression.

Sections du résumé

BACKGROUND
Restrictive lung disease leading to abnormal lung function in kidney transplant recipients is commonly associated with noninfectious complications or medications used for post-transplant immunosuppression. Herein, we report an interesting case of pediatric kidney transplant recipient with weight loss and abnormal spirometry who was diagnosed to have late-onset Pneumocystis pneumonia.
CASE REPORT
A 17-year-old male patient with a history of allergic rhinitis, mild persistent asthma, and deceased donor kidney transplant, performed 18 months prior, presented for routine evaluation of his asthma to the pulmonology clinic. He was clinically asymptomatic except for a weight loss of 8 kg over 6-month period prior to presentation. Patient's spirometry was suggestive of a restrictive pattern and further investigation using a high-resolution computed tomography (HRCT) of the chest showed bilateral diffuse ground-glass reticulonodular opacities with subpleural sparing suggestive of interstitial pneumonitis. A bronchoscopy with bronchoalveolar lavage revealed organisms consistent with Pneumocystis jirovecii on gomori-methenamine-silver (GMS) staining. Beta-d-glucan testing in serum revealed a level of >500 pg/mL (normal 0-59 pg/mL) further supportive of Pneumocystis jirovecii infection. Patient was treated with a 6-week course of trimethoprim-sulfamethoxazole. His weight loss and beta-d-glucan levels improved over a course of 6 months, and he continues to be on trimethoprim-sulfamethoxazole prophylaxis.
CONCLUSION
Late-onset Pneumocystis jirovecii infection in kidney transplant recipients can have an atypical presentation. Treating physicians should consider PJP in the differential diagnosis of unexplained weight loss in pediatric kidney transplant recipients, especially those receiving a large cumulative burden of immunosuppression.

Identifiants

pubmed: 37448256
doi: 10.1111/petr.14576
doi:

Substances chimiques

Trimethoprim, Sulfamethoxazole Drug Combination 8064-90-2

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14576

Informations de copyright

© 2023 Wiley Periodicals LLC.

Références

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Auteurs

Manpreet Grewal (M)

Division of Nephrology and Hypertension, Department of Pediatrics, Children's Hospital of Michigan, Detroit, Michigan, USA.
Department of Pediatrics, Central Michigan University College of Medicine, Mount Pleasant, Michigan, USA.

Ruma Srivastava (R)

Department of Pediatrics, Central Michigan University College of Medicine, Mount Pleasant, Michigan, USA.
Division of Pulmonology, Department of Pediatrics, Children's Hospital of Michigan, Detroit, Michigan, USA.

Jocelyn Y Ang (JY)

Department of Pediatrics, Central Michigan University College of Medicine, Mount Pleasant, Michigan, USA.
Division of Pediatric Infectious Diseases, Department of Pediatrics, Children's Hospital of Michigan, Detroit, Michigan, USA.
Department of Pediatrics, Wayne State University School of Medicine, Detroit, Michigan, USA.

Hossein Salimnia (H)

Department of Pediatrics, Central Michigan University College of Medicine, Mount Pleasant, Michigan, USA.
Division of Microbiology, Children's Hospital of Michigan, Detroit, Michigan, USA.

Amrish Jain (A)

Division of Nephrology and Hypertension, Department of Pediatrics, Children's Hospital of Michigan, Detroit, Michigan, USA.
Department of Pediatrics, Central Michigan University College of Medicine, Mount Pleasant, Michigan, USA.

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