Adolescent-onset TAFRO Syndrome with Malignant Nephrosclerosis-like Lesions

Intern Med. 2023 Aug 1;62(15):2223-2229. doi: 10.2169/internalmedicine.0529-22. Epub 2022 Dec 14.

Abstract

A 16-year-old Japanese girl developed a fever, thrombocytopenia, and renal dysfunction. Treatment was started with steroids, but cervical lymphadenopathy and ascites developed. A lymph node biopsy indicated TAFRO syndrome. The patient's renal function deteriorated, and dialysis was started. Refractory hypertension and subsequent encephalopathy developed. Treatment was started with an anti-IL-6 receptor antibody and an anti-CD20 monoclonal antibody. A kidney biopsy showed malignant nephrosclerosis-like microangiopathy and glomerular collapse due to narrowing of the small arteries. The majority of TAFRO syndrome cases are adult-onset, with glomerular microangiopathy. To our knowledge, this is the first report of adolescent-onset TAFRO syndrome presenting with malignant nephrosclerosis-like lesions associated with hypertension.

Keywords: TAFRO syndrome; adolescent onset; malignant hypertension.

MeSH terms

  • Adolescent
  • Adult
  • Castleman Disease* / complications
  • Castleman Disease* / diagnosis
  • Castleman Disease* / pathology
  • Edema / pathology
  • Female
  • Humans
  • Hypertension*
  • Kidney Diseases* / pathology
  • Kidney Glomerulus / pathology
  • Nephrosclerosis* / pathology

Supplementary concepts

  • Multi-centric Castleman's Disease