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2.
Pediatr Transplant ; 28(1): e14585, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-37489596

RESUMO

BACKGROUND: Cryptococcus neoformans is the third most common cause of invasive fungal infection in solid organ transplant (SOT) recipients. While cryptococcal infection can involve any organ, cases of myocarditis are exceedingly rare. METHODS: A retrospective chart review was completed for this case report. RESULTS: We present the case of a 21-year-old heart transplant recipient who developed disseminated cryptococcal infection with biopsy-proven cryptococcal myocarditis. CONCLUSIONS: Cryptococcal disease in SOT recipients poses diagnostic and therapeutic challenges. There are no current guidelines for the duration of cryptococcal myocarditis treatment. Repeat myocardial biopsy may play a role in guiding length of therapy.


Assuntos
Criptococose , Cryptococcus neoformans , Transplante de Coração , Miocardite , Humanos , Adulto Jovem , Adulto , Estudos Retrospectivos , Miocardite/complicações , Miocardite/diagnóstico , Criptococose/complicações , Criptococose/diagnóstico , Criptococose/tratamento farmacológico , Transplante de Coração/efeitos adversos
3.
Pediatr Transplant ; 27(5): e14492, 2023 08.
Artigo em Inglês | MEDLINE | ID: mdl-36860187

RESUMO

BACKGROUND: Malakoplakia occurs uncommonly at any age, but pediatric reports are exceptionally limited. Malakoplakia appears primarily in the urinary tract, although involvement of essentially all organs has been reported, cutaneous malakoplakia is very uncommon and liver involvement is the rarest. METHOD: We report the first pediatric case of concurrent hepatic and cutaneous malakoplakia in a pediatric liver transplant recipient. We also provide a literature review for cutaneous malakoplakia cases in children. RESULT: A 16-year-old male received a deceased-donor liver transplant for autoimmune hepatitis, present with the persistence of the liver mass of unknown etiology and cutaneous plaque-like lesions around the surgical scar. Core biopsies taken from the skin and abdominal wall lesions demonstrated histiocytes containing Michaelis-Gutmann bodies (MGB) revealing the diagnosis. The patient successfully was treated with antibiotics alone for 9 months without surgical intervention or a decrease in immunosuppressive therapy. CONCLUSION: This case demonstrates the need to include malakoplakia in the differential diagnosis of mass-forming lesions after solid transplantation and increase awareness of this very rare entity in pediatrics.


Assuntos
Transplante de Fígado , Malacoplasia , Masculino , Humanos , Criança , Adolescente , Transplante de Fígado/efeitos adversos , Malacoplasia/diagnóstico , Malacoplasia/etiologia , Malacoplasia/patologia , Doadores Vivos , Pele/patologia , Fígado/patologia
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