首页> 外文期刊>Journal of Medical Case Reports >Refractory immune thrombocytopenia successfully treated with high-dose vitamin D supplementation and hydroxychloroquine: two case reports
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Refractory immune thrombocytopenia successfully treated with high-dose vitamin D supplementation and hydroxychloroquine: two case reports

机译:大剂量维生素D补充和羟氯喹成功治疗难治性免疫性血小板减少症2例

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Introduction Immune thrombocytopenic purpura is thought to be characterized by an immune response against the host’s own platelets. If the thrombocytopenia is severe, patients are initially treated with high-dose steroids. Other more toxic second line treatments are considered if steroids fail. Here, we report the case of two patients in whom conventional treatment was unsuccessful but who responded to hydroxychloroquine and high-dose vitamin D replacement therapy. To the best of our knowledge, this is the first description of successful treatment for immune thrombocytopenia with high-dose vitamin D and hydroxychloroquine. Case presentation Case 1: We report the case of a 79-year-old Caucasian man who presented with high titer antinuclear antibodies, positive anti-SSA/Ro autoantibodies and clinically was felt to have an overlap of systemic lupus erythematosus and/or Sj?gren’s syndrome with profound life-threatening thrombocytopenia. There was no evidence of underlying malignancy. The patient’s platelet count significantly increased with vitamin D and hydroxychloroquine treatment, but upon vitamin D discontinuation his platelet levels plummeted. Hydroxychloroquine therapy was maintained throughout treatment. With reinstitution of high-dose vitamin D therapy, platelet counts were restored to normal levels. Case 2: We also report the case of an 87-year-old Caucasian woman who presented with high titer antinuclear antibodies, positive anti-SSA/Ro autoantibodies and was felt to have an overlap of systemic lupus erythematosus and/or Sj?gren’s syndrome with immune thrombocytopenia; she also had severely low levels of 25-hydroxy vitamin D (17ng/mL). There was no evidence of underlying malignancy. She responded to high-dose vitamin D replacement and hydroxychloroquine treatment, thereby alleviating the need for high-dose steroid treatment. She remains in remission while taking vitamin D, hydroxychloroquine and very low-dose prednisone. No untoward side effects were observed in either patient. Conclusions In our two case reports, we found an association between vitamin D deficiency and immune thrombocytopenia where platelet levels responded to vitamin D treatment and hydroxychloroquine but not to prednisone. We believe there may be synergism between vitamin D supplementation and hydroxychloroquine. The mechanism by which high-dose vitamin D results in increased platelet counts in immune thrombocytopenia patients is unknown. However, vitamin D has long been thought to play an immunomodulatory role, which may include a dampened immune response in patients with immune thrombocytopenia or other autoimmune diseases.
机译:简介免疫性血小板减少性紫癜被认为具有针对宿主自身血小板的免疫反应的特征。如果血小板减少严重,则首先应使用大剂量类固醇治疗患者。如果类固醇失败,则考虑使用其他毒性更大的二线治疗药物。在这里,我们报告了两名患者的病例,其中常规治疗未成功,但对羟氯喹和大剂量维生素D替代疗法有反应。据我们所知,这是首次使用大剂量维生素D和羟氯喹成功治疗免疫性血小板减少症。病例介绍病例1:我们报告了一个79岁的白人男子的病例,该男子表现出高滴度的抗核抗体,抗SSA / Ro自身抗体阳性,临床上被认为与系统性红斑狼疮和/或Sj有重叠?格林氏综合症,伴有严重威胁生命的血小板减少症。没有证据表明潜在的恶性肿瘤。维生素D和羟氯喹治疗后,患者的血小板计数显着增加,但是在维生素D停用后,其血小板水平骤然下降。在整个治疗过程中维持羟氯喹治疗。随着大剂量维生素D治疗的恢复,血小板计数恢复到正常水平。案例2:我们还报告了一个87岁的白种女人的情况,该女人表现出高滴度的抗核抗体,抗SSA / Ro自身抗体阳性,并被认为与系统性红斑狼疮和/或Sj?gren综合征重叠患有免疫性血小板减少症;她的25-羟基维生素D(17ng / mL)含量也很低。没有证据表明潜在的恶性肿瘤。她对大剂量维生素D替代和羟氯喹治疗产生了反应,从而减轻了对大剂量类固醇治疗的需求。服用维生素D,羟氯喹和极低剂量的泼尼松可使她保持缓解状态。两名患者均未观察到不良副作用。结论在我们的两个病例报告中,我们发现维生素D缺乏与免疫性血小板减少症之间存在关联,其中血小板水平对维生素D治疗和羟氯喹有反应,但对泼尼松无反应。我们认为补充维生素D和羟氯喹之间可能存在协同作用。大剂量维生素D导致免疫性血小板减少症患者血小板计数增加的机制尚不清楚。然而,长期以来人们一直认为维生素D起到免疫调节作用,其中可能包括免疫性血小板减少症或其他自身免疫性疾病患者的免疫反应减弱。

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