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Chronic brucellosis with hepatic brucelloma and AA amyloidosis in a patient with autosomal dominant polycystic kidney disease
Kollabathula, Arpitha; Vishwajeet, Vikarn; Gupta, Kirti; Mitra, Suvradeep; Sharma, Vibhav; Ray, Pallab; Bhalla, Ashish.
  • Kollabathula, Arpitha; Postgraduate Institute of Medical Education and Research. Department of Histopathology. Chandigarh. IN
  • Vishwajeet, Vikarn; Postgraduate Institute of Medical Education and Research. Department of Histopathology. Chandigarh. IN
  • Gupta, Kirti; Postgraduate Institute of Medical Education and Research. Department of Histopathology. Chandigarh. IN
  • Mitra, Suvradeep; Postgraduate Institute of Medical Education and Research. Department of Histopathology. Chandigarh. IN
  • Sharma, Vibhav; Postgraduate Institute of Medical Education and Research. Department of Internal Medicine. Chandigarh. IN
  • Ray, Pallab; Postgraduate Institute of Medical Education and Research. Department of Medical Microbiology. Chandigarh. IN
  • Bhalla, Ashish; Postgraduate Institute of Medical Education and Research. Department of Internal Medicine. Chandigarh. IN
Autops. Case Rep ; 10(1): 2019128, Jan.-Mar. 2020. ilus, tab
Artigo em Inglês | LILACS | ID: biblio-1052960
ABSTRACT
We describe an autopsy case of a 45-year-old male diagnosed with autosomal dominant polycystic kidney disease who presented with complaints of altered sensorium. The autopsy revealed multiple tumor-like masses in the liver, which on histological examination depicted multiple large suppurative granulomas with the presence of variable acid-fast coccobacilli (consistent with Brucella spp.). Interestingly, extensive amyloid deposition in multiple organs was noted. To the best of our knowledge, this is the first case of chronic brucellosis causing tumor-like abscesses in the liver accompanied by secondary systemic amyloidosis in a patient with underlying autosomal dominant polycystic kidney disease.
Assuntos


Texto completo: DisponíveL Índice: LILACS (Américas) Assunto principal: Rim Policístico Autossômico Dominante / Amiloidose Tipo de estudo: Estudo diagnóstico Limite: Humanos / Masculino Idioma: Inglês Revista: Autops. Case Rep Assunto da revista: Anatomia / Patologia Cl¡nica / Patologia Legal Ano de publicação: 2020 Tipo de documento: Artigo País de afiliação: Índia Instituição/País de afiliação: Postgraduate Institute of Medical Education and Research/IN

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Texto completo: DisponíveL Índice: LILACS (Américas) Assunto principal: Rim Policístico Autossômico Dominante / Amiloidose Tipo de estudo: Estudo diagnóstico Limite: Humanos / Masculino Idioma: Inglês Revista: Autops. Case Rep Assunto da revista: Anatomia / Patologia Cl¡nica / Patologia Legal Ano de publicação: 2020 Tipo de documento: Artigo País de afiliação: Índia Instituição/País de afiliação: Postgraduate Institute of Medical Education and Research/IN