Abstract

Introduction: Malignant hypertension (mHTN) damages multiple target organs, including the kidneys. mHTN has been regarded as one of the causes of secondary thrombotic microangiopathy (TMA); however, a high prevalence of complement gene abnormalities was recently reported in cohorts of mHTN. Case report: We herein describe a 47-year-old male who presented with severe hypertension, renal failure (serum creatinine (sCr): 11.6 mg/dL), heart failure, retinal hemorrhage, hemolytic anemia, and thrombocytopenia. Renal biopsy findings were consistent with acute hypertensive nephrosclerosis. The patient was diagnosed with secondary TMA associated with mHTN. However, his previous medical history of TMA of unknown origin and family history of atypical hemolytic uremic syndrome (aHUS) suggested as aHUS presenting mHTN, and genetic testing revealed a pathogenic C3 mutation (p.I1157T). The patient required plasma exchange and hemodialysis for 2 weeks and was able to withdraw from dialysis by antihypertensive therapy without eculizumab. Renal function gradually improved to a sCr level of 2.7 mg/dL under antihypertensive therapy for 2 years after the event. There was no recurrence, and renal function was preserved throughout a 3-year follow-up. Discussion: mHTN is a common presentation of aHUS. In cases of mHTN, abnormalities in complement-related genes may be involved in the development of the disease.

Author Details

Authors

• Chiaki Omiya¹
• Kenichi Koga¹
• Keisuke Nishioka¹
• Akira Sugawara¹
• Yuka Sugawara²
• Yoko Yoshida²
• Yoichiro Ikeda²
• Kensei Yahata¹

Departments

• ¹ Department of Nephrology, Osaka Red Cross Hospital, Osaka, and
• ² Department of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan

Address

Kenichi Koga, MD, PhD, Department of Nephrology, Osaka Red Cross Hospital, 5-30 Fudegasaki-cho, Tennoji-ku, Osaka-shi, Osaka 543-8555, Japan
Email: [email protected]

Citation