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孤立性抗Ro/SSA血小板减少症:新生儿狼疮的一种罕见特征。

Isolated anti-Ro/SSA thrombocytopenia: a rare feature of neonatal lupus.

作者信息

Ayadi Imene Dahmane, Ben Hamida Emira, Boukhris Mohamed Riadh, Bezzine Ahlem, Chaouachi Sihem, Marrakchi Zahra

机构信息

Department of Neonatology, Charles Nicolle Hospital, Tunis-El Manar University, Tunis, Tunisia.

出版信息

Pan Afr Med J. 2015 Nov 27;22:312. doi: 10.11604/pamj.2015.22.312.6839. eCollection 2015.

Abstract

We report a rare case of isolated thrombocytopenia related to anti-Ro/SSA antibodies. The mother was followed for unlabeled familial thrombocytopenia. The mother had positive anti-Ro/SSA antibodies. She was asymptomatic without skin lesions or other criteria neither of systemic lupus erythematosus nor other connective tissue disease. Pregnancy was uneventful. The postnatal examination was normal. On the first day of life, blood cells count showed thrombocytopenia at 40 x 10(9)/L. Within the second day of life, platelet level dropped to 20 x 10(9)/L. The management of thrombocytopenia included platelet transfusion and human immunoglobulin infusion. On the fifth day of life, there has been a drop in platelet count to 10 x 10(9)/L requiring renewed platelet transfusion and human immunoglobulin infusion. On the 10(th) of life platelets rate was stable around 60 x 10(9)/L. The infant had no evidence of cardiac, dermatologic or hepatobilary involvement initially or throughout follow up.

摘要

我们报告了一例罕见的与抗Ro/SSA抗体相关的孤立性血小板减少症病例。母亲因未明确诊断的家族性血小板减少症而接受随访。母亲抗Ro/SSA抗体呈阳性。她没有症状,没有皮肤病变,也不符合系统性红斑狼疮或其他结缔组织病的其他标准。孕期顺利。产后检查正常。出生第一天,血细胞计数显示血小板减少,为40×10⁹/L。出生第二天内,血小板水平降至20×10⁹/L。血小板减少症的治疗包括输注血小板和人免疫球蛋白。出生第五天,血小板计数降至10×10⁹/L,需要再次输注血小板和人免疫球蛋白。出生第10天时,血小板计数稳定在60×10⁹/L左右。婴儿最初及整个随访过程中均无心脏、皮肤或肝胆受累的证据。

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