Autoimmune thrombotic thrombocytopenic purpura associated with disseminated sarcoidosis: A case report

被引:0
作者
Billotte, Maxime [1 ]
Eszto, Peter [2 ]
Thomas, Benoit [3 ]
Groizard, Pierre [4 ]
Perez, Pierre [5 ]
Campagne, Julien [1 ,6 ]
机构
[1] Hop Robert Schuman, Med Interne, Vantoux, France
[2] Hop Robert Schuman, Reanimat, Vantoux, France
[3] Hop Robert Schuman, Lab Biol Med, Vantoux, France
[4] Hop Instruct Armees Legouest, Med Interne & Rhumatol, Metz, France
[5] Univ Lorraine, Ctr Hosp Reg Univ Nancy, Med Intens & Reanimat, Nancy, France
[6] Hop Robert Schuman, Rue Champ Montoy, F-57070 Vantoux, France
来源
EJHAEM | 2024年 / 5卷 / 01期
关键词
ADAMTS13; antibodies; case report; sarcoidosis; thrombotic thrombocytopenic purpura; MICROANGIOPATHY; DISEASES;
D O I
10.1002/jha2.848
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sarcoidosis is an inflammatory disease known to be associated with multiple autoimmune disorders. There is a restricted number of descriptions of the association between sarcoidosis and autoimmune thrombotic thrombocytopenic purpura (aTTP). We present the case of a 63-year-old woman admitted to the hospital to investigate a possible sarcoidosis who had hemolytic anemia and thrombocytopenia, with low ADAMTS13 activity and anti-ADAMTS13 antibodies, leading to a diagnosis of aTTP. Sarcoidosis was later confirmed and the two conditions evolved separately after 6 months, questioning the link between them. Clinicians should be aware of this rare cause of thrombocytopenia in patients with sarcoidosis, as aTTP is a life-threatening condition.
引用
收藏
页码:225 / 230
页数:6
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