|Year : 2015 | Volume
| Issue : 2 | Page : 276-277
Immunosuppressive treatment for immune thrombocytopenia which masked Graves' disease
Suleyman Baldane, Suleyman Hilmi Ipekci, Levent Kebapcilar
Department of Internal Medicine, Division of Endocrinology and Metabolism, Faculty of Medicine, Selcuk University, Konya, Turkey
|Date of Web Publication||8-Apr-2015|
Department of Internal Medicine, Division of Endocrinology and Metabolism, Selcuk University, 42075 Konya
Source of Support: None, Conflict of Interest: None
A 71-year-old female patient followed primary immune thrombocytopenia (ITP) was admitted to endocrinology unit with excessive sweating. We started methimazole for Graves' disease. Without any additional immunosuppressive treatment, at week 12 of methimazole therapy, thyroid stimulating hormone (TSH) levels returned to normal, and platelet counts rose to tolerable levels. When her hospital records were analyzed, they revealed that a year ago, when she had been diagnosed with ITP, her TSH values had been suppressed. After immunosuppressive therapy, her platelet values were maintained at normal levels, and during her control visits, her TSH levels were measured twice and were within normal limits. We think that immunosuppressive therapy for ITP without considering thyroid function tests may result in a transient euthyroid state, which potentially masks Graves' disease accompanying immunosuppressive therapy and associated recurrent ITP attacks.
Keywords: Graves′ disease, immune thrombocytopenia, methimazole
|How to cite this article:|
Baldane S, Ipekci SH, Kebapcilar L. Immunosuppressive treatment for immune thrombocytopenia which masked Graves' disease. J Family Med Prim Care 2015;4:276-7
|How to cite this URL:|
Baldane S, Ipekci SH, Kebapcilar L. Immunosuppressive treatment for immune thrombocytopenia which masked Graves' disease. J Family Med Prim Care [serial online] 2015 [cited 2020 May 27];4:276-7. Available from: http://www.jfmpc.com/text.asp?2015/4/2/276/154675
| Introduction|| |
Coexistence of hyperthyroidism and primary immune thrombocytopenia (ITP) is a rather rare condition. Therefore, little is known about the outcomes of these two diseases when associated. Underlying untreated Graves' disease leads to worsening of the ITP and rendering it refractory to standard therapy.  We report a case of Graves' disease masked by immunosuppressive therapy for ITP.
| Case Report|| |
A 71-year-old female patient presented with a complaint of excessive sweating for nearly a month to a hematology unit where she had been followed-up with after a diagnosis of ITP. Her laboratory tests revealed manifest hyperthyroidism in addition to thrombocytopenia, and hence she was referred to our endocrinology unit. On her physical examination, her pulse rate was 112 bpm, and her skin was warm and damp. In addition, a diffusely hypertrophic thyroid gland was palpated. Palpable lymphadenopathy and splenomegaly were not detected. On peripheral smear, only thrombocytopenia was found. Increased levels of anti-thyroid peroxidase, anti-thyroglobulin, and thyroid-stimulating antibody and enhanced uptake of radioactive iodine were observed, and the diagnosis of Graves' disease was confirmed. Methimazole therapy at daily doses of 30 mg was initiated. Without any additional immunosuppressive treatment, at week 12 of methimazole therapy, thyroid stimulating hormone (TSH) levels returned to normal, and platelet counts rose to tolerable levels.
When her hospital records were analyzed, they revealed that a year ago, when she had been diagnosed with ITP, her TSH values had been suppressed. At that time, the patient had not described any complaint suggesting hyperthyroidism. She had been given intravenous immune globulin (0.5 g/kg/day for 4 days) and oral steroid (1 mg/kg/day) for the treatment of ITP. The patient, whose platelet counts returned to being within normal limits, was followed-up with for 6 months. During this period, her platelet values were maintained at normal levels, and during her control visits, her TSH levels were measured twice and were within normal limits. The patient's laboratory test results are shown in chronological order [Table 1].
| Discussion|| |
The association between Graves' disease and thrombocytopenia was first defined in 1931.  Afterwards, concomitancy of autoimmune thyroid diseases such as Hashimoto thyroiditis and Graves' disease with ITP has been reported many times. 
In Graves' disease, the lifespan of platelets is shortened significantly, and moderate degrees of thrombocytopenia are frequently seen.  The potential mechanism involved in this process is increased phagocytic activity of the reticuloendothelial system.  The association between ITP and Graves' disease is explained by immune dysregulation, which is the main mechanism underlying both diseases and involves an increase in the levels of antiplatelet and anti-thyroid antibodies in these patients. 
Because of the strong fundamental autoimmune mechanism underlying both diseases, it is known that the treatment of associated autoimmune thyroid disorder contributes to the remission of ITP. It has been reported that the treatment of underlying Graves' disease in patients refractory to standard immunosuppressive therapy ensured remission of ITP.  Besides, only anti-thyroid treatment without additional immunosuppressive treatment enabled remission of ITP. 
In our case, Graves' disease had been overlooked during the diagnostic work-up for ITP. Although spontaneous remissions can be seen in Graves' disease, we think that immunosuppressive therapy given for the treatment of ITP-induced a transient euthyroidism in Graves' disease. During the 6 months following ITP therapy of our patient, whose TSH values remained at normal levels, Graves' disease and concomitant ITP recurrences were observed, and only anti-thyroid therapy increased platelet counts to tolerable levels.
| Conclusion|| |
In the presence of thrombocytopenia, the patients should be carefully evaluated for hyperthyroidism. It should be kept in mind that immunosuppressive therapy without considering thyroid function tests may result in a transient euthyroid state, which potentially masks Graves' disease accompanying immunosuppressive therapy and associated recurrent ITP attacks.
| References|| |
Cheung E, Liebman HA. Thyroid disease in patients with immune thrombocytopenia. Hematol Oncol Clin North Am 2009;23:1251-60.
Jackson AS. Acute hemorrhagic purpura associated with exopthalmic goiter. JAMA 1931;96:38-9.
Brent GA. Clinical practice. Graves' disease. N Engl J Med 2008;358:2594-605.
Panzer S, Haubenstock A, Minar E. Platelets in hyperthyroidism: Studies on platelet counts, mean platelet volume, 111-indium-labeled platelet kinetics, and platelet-associated immunoglobulins G and M. J Clin Endocrinol Metab 1990;70:491-6.
Gill H, Hwang YY, Tse E. Primary immune thrombocytopenia responding to antithyroid treatment in a patient with Graves' disease. Ann Hematol 2011;90:223-4.
Sugimoto K, Sasaki M, Isobe Y, Tamayose K, Hieda M, Oshimi K. Improvement of idiopathic thrombocytopenic purpura by antithyroid therapy. Eur J Haematol 2005;74:73-4.
|This article has been cited by|
||The effect of anti-thyroid antibodies positivity on children with primary immune thrombocytopenia
| ||Suzan O. Mousa,Gamal T. Soliman,Ahmed A.-F. Saedii,Emad N. Hameed |
| ||Pediatric Hematology and Oncology. 2017; : 1 |
|[Pubmed] | [DOI]|
||Elevated interleukin-1ß in peripheral blood mononuclear cells contributes to the pathogenesis of autoimmune thyroid diseases, especially of Hashimoto thyroiditis
| ||Li Sun,Xiaoxu Zhang,Fang Dai,Jijia Shen,Cuiping Ren,Chunlin Zuo,Qiu Zhang |
| ||Endocrine Research. 2016; : 1 |
|[Pubmed] | [DOI]|