[Advances in pathophysiology, diagnosis and treatment of adult severe-associated thrombotic microangiopathy]

Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2023 Dec;35(12):1335-1339. doi: 10.3760/cma.j.cn121430-20230808-00596.
[Article in Chinese]

Abstract

Thrombotic microangiopathy (TMA) is a group of highly heterogeneous, acute and severe clinicopathological syndromes, characterized by microangiopathic hemolytic anemia (MAHA), thrombocytopenia and ischemic injury of end organs. TMA has the characteristics of dangerous condition, multiple organ involvement and high mortality. Patients with severe TMA need to be admitted to intensive care unit (ICU) for organ function support therapy. Early and rapid evaluation, differential diagnosis, and timely and effective treatment are the key to improve the prognosis of TMA patients. Here, we review the pathophysiological changes, diagnosis differential diagnosis, and treatment of the severe TMA in adult.

Publication types

  • Review
  • English Abstract

MeSH terms

  • Adult
  • Anemia, Hemolytic* / diagnosis
  • Anemia, Hemolytic* / therapy
  • Diagnosis, Differential
  • Humans
  • Purpura, Thrombotic Thrombocytopenic* / diagnosis
  • Purpura, Thrombotic Thrombocytopenic* / therapy
  • Thrombotic Microangiopathies* / diagnosis
  • Thrombotic Microangiopathies* / therapy
  • Treatment Outcome