Case Reports
Thrombotic Thrombocytopenic Purpura and Graves Disease

https://doi.org/10.1097/MAJ.0b013e31812e9735Get rights and content

ABSTRACT

Patients with an autoimmune disease have a propensity for development of a second autoimmune disease. We report the first instance of a patient with both idiopathic thrombotic thrombocytopenic purpura (TTP) and Graves disease. The TTP remitted with a combination of plasmapheresis and prednisone. Methimazole led to sustained remission of the hyperthyroid state within 6 weeks. Although hyperthyroidism may induce immune imbalance causing autoimmunity, it is unclear if this influenced the development of TTP in our patient and if treatment of hyperthyroidism alone could have resulted in the cure of both diseases.

Section snippets

Case Report

A 49-year-old Caucasian woman presented with a 1-week history of progressive exertional dyspnea, palpitations, headache, fever, chills, and lower extremity bruises. She reported no visual changes, confusion, weight loss, diaphoresis, and diarrhea. Physical examination revealed a systolic flow murmur, conjunctival pallor, and petechiae over her lower extremities. Ophthalmic signs of Graves disease and goiter were absent. She was afebrile.

Her laboratory evaluation was as follows: hemoglobin 7.4 

Discussion

Thrombotic thrombocytopenic purpura is associated with autoimmune disorders such as autoimmune hemolytic anemia7 and systemic lupus erythematosus.8 Graves disease is frequently associated with ITP but never with TTP.6

The pathogenesis of Graves disease has been linked to genetic factors such as HLA-DR3 and cytotoxic T-lymphocyte antigen-4 (CTLA-4) and to environmental factors such as stress, female sex steroids, and certain infections (Yersinia enterocolitica, retroviruses).9 The etiology of

References (15)

There are more references available in the full text version of this article.

Cited by (10)

View all citing articles on Scopus
View full text