The Clinical and Histopathological Feature of Renal Manifestation of TAFRO Syndrome.

Abstract

INTRODUCTION:

Thrombocytopenia, anasarca, myelofibrosis, renal dysfunction, and organomegaly (TAFRO) syndrome is a severe subtype of idiopathic multicentric Castleman's disease, characterized by thrombocytopenia, anasarca, fever, reticulin myelofibrosis, and organomegaly. Renal complication of this disease can be life-threatening and sometimes requires hemodialysis, but it has not been elucidated in detail.

METHODS:

Case-series was designed to evaluate the renal histology of patients with TAFRO syndrome treated at our hospital.

RESULTS:

Seven patients were eligible to the criteria. All of them had severe diuretic-resistant anasarca and 6 of 7 had mild proteinuria (<1 g daily). On light microscopy, all patients showed glomerular endotheliopathy characterized by endothelial cell swelling and a double contour of the glomerular basement membrane with mesangiolysis or mesangial loosening. Immunofluorescent staining and electron microscopy did not detect immune deposits in any patient. Electron microscopy revealed endothelial cell swelling with diffuse expansion of the subendothelial space, loss of mesangial architecture, and loss of endothelial cell fenestrations. Treatment with glucocorticoids and molecular-targeting agents, including tocilizumab and rituximab, improved renal dysfunction and anasarca. In 4 of 7 patients with persistent thrombocytopenia, hemorrhagic events occurred despite platelet transfusion or thrombopoietin receptor antagonist therapy.

CONCLUSION:

Severe diuretic-resistant anasarca with mild proteinuria and severe glomerular endotheliopathy were common characteristics of renal dysfunction due to TAFRO syndrome. In addition, endothelial changes mediated via interleukin (IL)-6 and vascular endothelial growth factor (VEGF) that lead to vascular hyperpermeability and water leakage might contribute to anasarca, because molecular-targeting therapy directed against IL-6 or VEGF improved renal dysfunction and severe endothelial damage.

• Authors: Hiroki Mizuno, Naoki Sawa, Shun Watanabe, Daisuke Ikuma, Akinari Sekine, Masahiro Kawada, Masayuki Yamanouchi, Eiko Hasegawa, Tatsuya Suwabe, Junichi Hoshino, Kenmei Takaichi, Keiichi Kinowaki, Takeshi Fujii, Kenichi Ohashi, Michio Nagata, Yutaka Yamaguchi, Yoshifumi Ubara
• Journal: Kidney international reports (Kidney Int Rep) Vol. 5 Issue 8 Pg. 1172-1179 (Aug 2020) ISSN: 2468-0249 [Electronic] United States
• PMID: 32775816 (Publication Type: Journal Article)
• Copyright: © 2020 International Society of Nephrology. Published by Elsevier Inc.