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狼疮性肺炎:新生儿狼疮罕见表现的病例报告

Lupus Pneumonitis: Case Report of a Rare Manifestation of Neonatal Lupus.

作者信息

Barreto Mota Ricardo, Santos Nuno Rodrigues, Éden Paulo, Rodrigues Mariana, Brito Iva, Soares Henrique

机构信息

Neonatology Department, Centro Hospitalar Universitário de São João, Porto, Portugal.

Pediatric Cardiology Department, Centro Hospitalar Universitário São João, Porto, Portugal.

出版信息

J Investig Med High Impact Case Rep. 2022 Jan-Dec;10:23247096221077815. doi: 10.1177/23247096221077815.

Abstract

Neonatal lupus is a rare entity, secondary to placental transfer of antibodies from mothers with immune-mediated conditions. While pulmonary involvement is common in lupus, its incidence in neonates is extremely rare, with very few cases being reported in the literature. The authors report a case of a neonate whose mother was diagnosed with systemic lupus erythematosus, with a prenatal diagnosis of third-degree atrioventricular block. While initially admitted in the neonatal intensive care unit with no need for organ support, he presented progressive respiratory failure, initially attributed to sepsis. Favorable clinical progression after pacemaker placement allowed ventilatory weaning, but respiratory failure was again apparent. Chest computer tomography revealed areas of ground-glass lesions, raising the suspicion for lupus pneumonitis. He was started on immunoglobulin and corticosteroids, with clinical improvement. The authors consider this case to be relevant due to the rarity of acute lupus pneumonitis in neonates, alerting that it must be considered a differential diagnosis in neonates with prolonged ventilator dependency.

摘要

新生儿狼疮是一种罕见病症,继发于患有免疫介导疾病的母亲经胎盘传递抗体。虽然肺部受累在狼疮中很常见,但其在新生儿中的发病率极其罕见,文献报道的病例极少。作者报告了一例新生儿病例,其母亲被诊断为系统性红斑狼疮,产前诊断为三度房室传导阻滞。该新生儿最初入住新生儿重症监护病房时无需器官支持,但随后出现进行性呼吸衰竭,最初归因于败血症。植入起搏器后临床进展良好,得以撤机,但呼吸衰竭再次出现。胸部计算机断层扫描显示磨玻璃样病变区域,怀疑为狼疮性肺炎。给予免疫球蛋白和皮质类固醇治疗后,临床症状改善。鉴于新生儿急性狼疮性肺炎罕见,作者认为该病例具有相关性,并提醒对于呼吸机依赖时间延长的新生儿,必须考虑将其作为鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fb/9016583/dea8c0b5feb3/10.1177_23247096221077815-fig1.jpg

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