Hepatic Campylobacter jejuni infection in patients with Castleman‐Kojima disease (idiopathic multicentric Castleman disease with thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly (TAFRO) syndrome). Issue 10 (20th October 2019)
- Record Type:
- Journal Article
- Title:
- Hepatic Campylobacter jejuni infection in patients with Castleman‐Kojima disease (idiopathic multicentric Castleman disease with thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly (TAFRO) syndrome). Issue 10 (20th October 2019)
- Main Title:
- Hepatic Campylobacter jejuni infection in patients with Castleman‐Kojima disease (idiopathic multicentric Castleman disease with thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly (TAFRO) syndrome)
- Authors:
- Kageyama, Chihiro
Igawa, Takuro
Gion, Yuka
Iwaki, Noriko
Tabata, Tetsuya
Tanaka, Takehiro
Kondo, Eisei
Sakai, Hajime
Tsuneyama, Koichi
Nomoto, Kazuhiro
Noguchi, Hiroko
Yoshino, Tadashi
Yokota, Kenji
Sato, Yasuharu - Abstract:
- Abstract : Castleman‐Kojima disease, also known as idiopathic multicentric Castleman disease with TAFRO syndrome (iMCD‐TAFRO), is a recently recognized systemic inflammatory disorder with a characteristic series of clinical symptoms, including thrombocytopenia (T), anasarca (A), fever (F), reticulin fibrosis (R), and organomegaly (O). Patients with iMCD‐TAFRO often develop severe abdominal pain, elevated alkaline phosphatase levels, and systemic inflammation, but the etiological factors are unknown. To investigate the potential role of bacterial infection in the pathogenesis of iMCD‐TAFRO, we performed polymerase chain reaction (PCR) for the bacterial 16S rRNA gene with DNA extracted from liver specimens of three patients with iMCD‐TAFRO, four patients with amyotrophic lateral sclerosis, and seven patients with inflammatory conditions. Sequencing of the PCR product showed 99% DNA sequence identity with Campylobacter jejuni in all three patients with iMCD‐TAFRO and in two patients with inflammatory conditions. Immunohistochemical and electron microscopy analyses could not identify C. jejuni in patients with iMCD‐TAFRO. The findings indicated that C. jejuni infection is not the pathological cause of iMCD‐TAFRO; however, this ubiquitous bacterium may play a role in uncontrolled systemic hypercytokinemia, possibly through the development of cross‐reactive autoantibodies.
- Is Part Of:
- Pathology international. Volume 69:Issue 10(2019)
- Journal:
- Pathology international
- Issue:
- Volume 69:Issue 10(2019)
- Issue Display:
- Volume 69, Issue 10 (2019)
- Year:
- 2019
- Volume:
- 69
- Issue:
- 10
- Issue Sort Value:
- 2019-0069-0010-0000
- Page Start:
- 572
- Page End:
- 579
- Publication Date:
- 2019-10-20
- Subjects:
- Castleman‐Kojima disease -- etiology -- multicentric Castleman disease -- TAFRO syndrome
Pathology -- Periodicals
616.07 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=pin ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/pin.12856 ↗
- Languages:
- English
- ISSNs:
- 1320-5463
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6412.823000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 16292.xml