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The use of eculizumab in Capnocytophaga canimorsus associated thrombotic microangiopathy: a case report.
Bjørkto, Magnus Holter; Barratt-Due, Andreas; Nordøy, Ingvild; Dörje, Christina; Galteland, Eivind; Lind, Andreas; Hilli, Abdulkarim; Aukrust, Pål; Mjøen, Geir.
Affiliation
  • Bjørkto MH; Department of Transplant Medicine, Oslo University Hospital, Birch-Reichenwaldsgate 34, NO-0483, Oslo, Norway. mbjorkto@gmail.com.
  • Barratt-Due A; Division of Critical care and Emergencies, Oslo University Hospital, Oslo, Norway.
  • Nordøy I; Section for Clinical Immunology and Infectious Diseases, Oslo University Hospital, Oslo, Norway.
  • Dörje C; Research Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
  • Galteland E; Department of Transplant Medicine, Oslo University Hospital, Birch-Reichenwaldsgate 34, NO-0483, Oslo, Norway.
  • Lind A; Department of Haematology, Oslo University Hospital, Oslo, Norway.
  • Hilli A; Department of Microbiology, Oslo University Hospital, Oslo, Norway.
  • Aukrust P; Department of Internal Medicine, Diakonhjemmet Hospital, Oslo, Norway.
  • Mjøen G; Section for Clinical Immunology and Infectious Diseases, Oslo University Hospital, Oslo, Norway.
BMC Infect Dis ; 21(1): 137, 2021 Feb 01.
Article in En | MEDLINE | ID: mdl-33526010
ABSTRACT

BACKGROUND:

The use of complement inhibition is well established for complement mediated thrombotic microangiopathy, but its role in secondary forms of thrombotic microangiopathy is debated. We here present a case of thrombotic microangiopathy triggered by Capnocytophaga canimorsus, illustrating the diagnostic difficulties in discriminating between different thrombotic microangiopathies, and the dilemmas regarding how to treat this disease entity. CASE PRESENTATION A previously healthy 56-year-old woman presented with fever and confusion. She was diagnosed with sepsis from Capnocytophaga canimorsus and thrombotic microangiopathy. Marked activation of both T-cells, endothelium and complement were documented. She was successfully treated with antimicrobial therapy, the complement inhibitor eculizumab and splenectomy. After several weeks, a heterozygote variant in complement factor B was localized, potentially implying the diagnosis of a complement mediated TMA over an isolated infection related TMA.

CONCLUSIONS:

We discuss the possible interactions between complement activation and other findings in severe infection and argue that complement inhibition proved beneficial to this patient's rapid recovery.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Capnocytophaga / Complement Activation / Complement Inactivating Agents / Thrombotic Microangiopathies / Antibodies, Monoclonal, Humanized Type of study: Etiology_studies / Risk_factors_studies Limits: Female / Humans / Middle aged Country/Region as subject: Europa Language: En Journal: BMC Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Capnocytophaga / Complement Activation / Complement Inactivating Agents / Thrombotic Microangiopathies / Antibodies, Monoclonal, Humanized Type of study: Etiology_studies / Risk_factors_studies Limits: Female / Humans / Middle aged Country/Region as subject: Europa Language: En Journal: BMC Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2021 Document type: Article Affiliation country: