A 62-year-old male who was receiving prednisolone and methotrexate for scleroderma and rheumatoid arthritis complained of diarrhea and vomiting, and was transferred to our hospital for detailed examination and treatment of renal dysfunction and thrombocytopenia. Hemolytic anemia and crushed erythrocytes were found during the patient's course; therefore, we suspected thrombotic microangiopathy (TMA). His ADAMTS13 activity was 60.3% and his ADAMTS13 inhibitor was under 0.5. In addition, his blood culture was positive for , and we finally diagnosed -associated TMA (pTMA). The patient was treated with antibiotics and hemodialysis. The patient recovered and was discharged on the 45 hospital day. Adult pTMA cases are remarkably rare. We herein report a successfully treated adult case of pTMA.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101476PMC
http://dx.doi.org/10.1515/med-2020-0030DOI Listing

Publication Analysis

Top Keywords

thrombotic microangiopathy
8
-associated thrombotic
4
microangiopathy immunosuppressed
4
immunosuppressed adult
4
adult 62-year-old
4
62-year-old male
4
male receiving
4
receiving prednisolone
4
prednisolone methotrexate
4
methotrexate scleroderma
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!