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Hypergammaglobulinemic Purpura of Waldenstrom (HGPW) in Pregnancy: A Rare Case Report

机译:Waldenstrom(HGPW)的妊娠性高γ-γ线性紫癜:罕见病例报告

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Hypergammaglobulinemic purpura of Waldenstrom (HGP)is a rare skin condition first described by Waldenstrom in1943. It presents as recurring purpura, elevated erythrocytesedimentation rate, mild anemia, hypergammaglobulinemiaand the presence of circulating immune complexes. Itcan be primary or secondary when associated with otherautoimmune diseases, especially Sjogren’s and lupus erythematosus.It usually affects females of reproductive-agegroup, i.e., between 18 to 40 years of age. It is usually abenign condition which does not require extensive investigationand treatment in its primary form. Limited literatureis available of its occurrence in pregnancy in whichcase HGPW requires prompt diagnosis and treatment forbetter fetal and maternal outcome. The presence of anti-Roantibodies in the maternal serum may lead to congenital heart block in 1–2% of pregnancies, neonatal lupus rash inaround 10–20% of cases with nine times risk of recurrence.Circulating immunoglobulins may lead to IUGR,preeclampsia, anemia or even IUD. Successful fetal andmaternal outcome is possible in current and subsequentpregnancies if HGPW is diagnosed and managed on time.
机译:Waldenstrom(HGP)的高伽玛球蛋白性紫癜是一种罕见的皮肤病,由Waldenstrom于1943年首次描述。它表现为反复发作的紫癜,红细胞沉降率升高,轻度贫血,高球蛋白血症和循环免疫复合物的存在。与其他自身免疫性疾病(尤其是干燥的红斑狼疮和红斑狼疮)有关时,它可能是原发性或继发性疾病。它通常会影响年龄在18至40岁之间的育龄女性。它通常是良性疾病,不需要以其主要形式进行广泛的调查和治疗。关于其在妊娠中的发生的文献有限,在这种情况下,HGPW需要迅速诊断和治疗以改善胎儿和产妇的预后。孕产妇血清中存在抗罗氏抗体可能会导致1-2%的孕妇发生先天性心脏传导阻滞,约占10%到20%的新生儿狼疮皮疹的发生率是复发的9倍。贫血甚至宫内节育器。如果及时诊断和处理HGPW,则当前和以后的妊娠都可能成功获得胎儿和母亲的预后。

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