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一名可能患有灾难性抗磷脂综合征的婴儿出现皮肤坏死复发。

Recurrence of cutaneous necrosis in an infant with probable catastrophic antiphospholipid syndrome.

作者信息

Camacho-Lovillo Soledad, Bernabeu-Wittel Jose, Iglesias-Jimenez Estíbaliz, Falcón-Neyra Doloresm, Neth Olaf

机构信息

Department of Pediatric Infectious Diseases and Immunology, Hospital Infantil Virgen del Rocío, Seville, Spain.

出版信息

Pediatr Dermatol. 2013 Jul-Aug;30(4):e63-4. doi: 10.1111/j.1525-1470.2012.01832.x. Epub 2012 Sep 7.

Abstract

We present the case of a 3-month-old child with probable catastrophic antiphospholipid syndrome who, after initial successful management with immunomodulary therapies including rituximab, experienced a cutaneous relapse. This rare event was successfully re-treated with repeated administration of rituximab, supporting its role in the control of this disorder. Dermatologic manifestations may be the main clinical presentation of antiphospholipid syndrome, a possible underdiagnosed but potentially fatal pathology.

摘要

我们报告了一例3个月大的疑似灾难性抗磷脂综合征患儿,该患儿在最初使用包括利妥昔单抗在内的免疫调节疗法成功治疗后,出现了皮肤复发。这一罕见事件通过重复使用利妥昔单抗成功再次治疗,支持了其在控制该疾病中的作用。皮肤表现可能是抗磷脂综合征的主要临床表现,这是一种可能未被充分诊断但潜在致命的疾病。

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