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An Unusual Case of Seronegative Cryoglobulinemic Glomerulonephritis with Dominant Organized IgA Deposits Associated with Staphylococcal Infection: Casual or Causal Relationship?
De La Flor Merino, José C; Apaza, Jacqueline; Díaz, Francisco; Sandoval, Edna; Valga, Francisco; Villa, Daniel; Marschall, Alexander; Abascal, María Luisa; Rivas, Andrea; Cieza, Michael.
Afiliação
  • De La Flor Merino JC; Department of Nephrology, Hospital Central Defense Gomez Ulla, Madrid, Spain.
  • Apaza J; Department of Nephrology, Hospital Fuensanta, Madrid, Spain.
  • Díaz F; Department of Anatomic Pathology, Hospital Gregorio Marañón, Madrid, Spain.
  • Sandoval E; Department of Hematology, Hospital Central Defense Gomez Ulla, Madrid, Spain.
  • Valga F; Department of Nephrology, Hospital Universitario Doctor Negrin de Gran Canarias, Las Palmas de Gran Canaria, Spain.
  • Villa D; Department of Nephrology, Clinica Universidad de Navarra, Pamplona, Spain.
  • Marschall A; Department of Cardiology, Hospital Central Defense Gomez Ulla, Madrid, Spain.
  • Abascal ML; Department of Anatomic Pathology, Hospital Gregorio Marañón, Madrid, Spain.
  • Rivas A; Department of Nephrology, Hospital Nacional Cayetano Heredia, Lima, Peru.
  • Cieza M; Chief of the Teaching Coordination Unit Universidad Peruana Cayetano Heredia, Lima, Peru.
Glomerular Dis ; 3(1): 140-147, 2023.
Article em En | MEDLINE | ID: mdl-37901697
ABSTRACT

Introduction:

Cryoglobulinemia refers to the presence of cryoglobulins (CGs) in the serum, encompassing a group of diseases caused by the type of circulating GC. Cryoglobulinemic glomerulonephritis (CryoGN) is the principal manifestation of renal involvement. The diagnosis may be challenging because the hallmark of cryoglobulinemia is the detection of CG in the serum. However, cases of CryoGN without serological evidence of CGs are not uncommon in clinical practice, often diagnosed by anatomopathological findings in the renal biopsy. Case Presentation We report the case of an 86-year-old male who developed renal impairment, nephritic syndrome, and nephrotic-range proteinuria, without serological evidence of CGs, associated with staphylococcal bacteremia without apparent focus. Renal biopsy and pathological examination showed a membranoproliferative glomerulonephritis pattern with CD61-negative pseudothrombi. Immunofluorescence microscopy showed atypical IgA-dominant deposits. Electron microscopy revealed amorphous subendothelial and mesangial deposits and organized electrodense deposits within capillary loops (pseudothrombi) with microtubular substructure measuring 20-40 nm in thickness. These findings were consistent with seronegative CryoGN and microtubular organized atypical IgA-dominant deposits.

Discussion:

In this report, we discuss the clinical, analytical, and histopathological findings of a rare case of CryoGN without serological evidence of CGs. Regarding the etiology that triggered the glomerular disease in our patient, we conducted an exhaustive study in order to determine the underlying cause of CryoGN. At the time of biopsy, the patient had an active staphylococcal bacteremia. There are reports that postulate that staphylococcal antigens drive activation of immune system and in consequence, could cause this rare form of IgA-dominant glomerulonephritis with cryoglobulinemic features. After ruling out other causes of cryoglobulinemia, we discuss a plausible causal relationship of the staphylococcal infection in the pathogenesis of CryoGN in our patient.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Glomerular Dis Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Glomerular Dis Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Espanha
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