Evolving idiopathic multicentric Castleman disease with thrombocytopenia, anasarca, fever/hyperinflammation, renal dysfunction and organomegaly presenting with severe hypoalbuminaemia, serositis and bicytopenia before lymphadenopathy.
- DOI
- 10.1136/bcr-2026-274330
- Published
- 2026-09-17
- Container
- BMJ Case Rep
- Publisher
- Not recorded
- Open access
- no
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Cite this work
BibTeX
@article{allodium:10.1136/bcr-2026-274330,
title = {Evolving idiopathic multicentric Castleman disease with thrombocytopenia, anasarca, fever/hyperinflammation, renal dysfunction and organomegaly presenting with severe hypoalbuminaemia, serositis and bicytopenia before lymphadenopathy.},
author = {Kachope J and Muradov O.},
year = {2026},
journal = {BMJ Case Rep},
doi = {10.1136/bcr-2026-274330},
url = {https://doi.org/10.1136/bcr-2026-274330}
}RIS
TY - JOUR TI - Evolving idiopathic multicentric Castleman disease with thrombocytopenia, anasarca, fever/hyperinflammation, renal dysfunction and organomegaly presenting with severe hypoalbuminaemia, serositis and bicytopenia before lymphadenopathy. AU - Kachope J AU - Muradov O. PY - 2026 JO - BMJ Case Rep DO - 10.1136/bcr-2026-274330 UR - https://doi.org/10.1136/bcr-2026-274330 ER -
APA
J, K., & O., M. (2026). Evolving idiopathic multicentric Castleman disease with thrombocytopenia, anasarca, fever/hyperinflammation, renal dysfunction and organomegaly presenting with severe hypoalbuminaemia, serositis and bicytopenia before lymphadenopathy.. BMJ Case Rep. https://doi.org/10.1136/bcr-2026-274330
Source records
- europe-pmc · retrieved 2026-09-25T19:57:39.984Z