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Can COVID-19 impact the natural history of paracoccidioidomycosis? Insights from an atypical chronic form of the mycosis
Souza, César Augusto Tomaz de; Ponce, Cesar Cilento; Klautau, Gisele Burlamaqui; Costa, André Nathan; Queiroz, Wladimir; Patzina, Rosely Antunes; Benard, Gil; Lindoso, José Angelo Lauletta.
  • Souza, César Augusto Tomaz de; Instituto de Infectologia Emilio Ribas. São Paulo. BR
  • Ponce, Cesar Cilento; Instituto de Infectologia Emilio Ribas. São Paulo. BR
  • Klautau, Gisele Burlamaqui; Instituto de Infectologia Emilio Ribas. São Paulo. BR
  • Costa, André Nathan; Universidade de São Paulo. Faculdade de Medicina. Departamento de Cardio-Pneumologia. São Paulo. BR
  • Queiroz, Wladimir; Instituto de Infectologia Emilio Ribas. São Paulo. BR
  • Patzina, Rosely Antunes; Instituto de Infectologia Emilio Ribas. São Paulo. BR
  • Benard, Gil; Universidade de São Paulo. Faculdade de Medicina. Instituto de Medicina Tropical de São Paulo. São Paulo. BR
  • Lindoso, José Angelo Lauletta; Instituto de Infectologia Emilio Ribas. São Paulo. BR
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1529448
ABSTRACT
ABSTRACT Paracoccidioidomycosis (PCM) is a systemic fungal infection caused by Paracoccidioides spp. It can occur as an acute/subacute form (A/SAF), a chronic form (CF) and rarely as a mixed form combining the features of the two aforementioned forms in an immunocompromised patient. Here, we report a 56-year-old male patient with CF-PCM who presented with atypical manifestations, including the development of an initial esophageal ulcer, followed by central nervous system (CNS) lesions and cervical and abdominal lymphatic involvement concomitant with severe SARS-CoV-2 infection. He was HIV-negative and had no other signs of previous immunodeficiency. Biopsy of the ulcer confirmed its mycotic etiology. He was hospitalized for treatment of COVID-19 and required supplemental oxygen in the intensive unit. The patient recovered without the need for invasive ventilatory support. Investigation of the extent of disease during hospitalization revealed severe lymphatic involvement typical of A/SAF, although the patient`s long history of high-risk exposure to PCM, and lung involvement typical of the CF. Esophageal involvement is rare in non-immunosuppressed PCM patients. CNS involvement is also rare. We suggest that the immunological imbalance caused by the severe COVID-19 infection may have contributed to the patient developing atypical severe CF, which resembles the PCM mixed form of immunosuppressed patients. Severe COVID-19 infection is known to impair the cell-mediated immune response, including the antiviral response, through T-lymphopenia, decreased NK cell counts and T-cell exhaustion. We hypothesize that these alterations would also impair antifungal defenses. Our case highlights the potential influence of COVID-19 on the course of PCM. Fortunately, the patient was timely treated for both diseases, evolving favorably.


Texto completo: DisponíveL Índice: LILACS (Américas) Idioma: Inglês Revista: Rev. Inst. Med. Trop. São Paulo (Online) Assunto da revista: Medicina Tropical Ano de publicação: 2023 Tipo de documento: Artigo País de afiliação: Brasil Instituição/País de afiliação: Instituto de Infectologia Emilio Ribas/BR / Universidade de São Paulo/BR

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Texto completo: DisponíveL Índice: LILACS (Américas) Idioma: Inglês Revista: Rev. Inst. Med. Trop. São Paulo (Online) Assunto da revista: Medicina Tropical Ano de publicação: 2023 Tipo de documento: Artigo País de afiliação: Brasil Instituição/País de afiliação: Instituto de Infectologia Emilio Ribas/BR / Universidade de São Paulo/BR