白细胞介素-36受体拮抗剂突变携带者与泛发性脓疱型银屑病的急性呼吸窘迫综合征。

Q3 Medicine
Avital Baniel, Efrat Bar-Ilan, Yuval Hilerowicz, Ilan Merdler, Eden Shkury, Ofer Sarig, Marina Eskin-Schwartz, Eli Sprecher
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引用次数: 0

摘要

背景:冯-祖姆布什泛发性脓疱型银屑病是银屑病的一种罕见变异型,通常伴有全身症状,有时甚至危及生命。泛发性脓疱型银屑病有时会在妊娠期出现:一名 31 岁的女性患者,有精神分裂症病史和反复发作的妊娠相关性脓疱型银屑病,在第五次妊娠的第 22 周因全身脓疱性皮疹入住我科。临床和组织病理学检查均提示为泛发性脓疱型银屑病(von Zumbusch 型)。住院期间,她出现了急性呼吸困难、发烧、心动过速和明显的白细胞增多。大量检查未能发现感染、心脏或肺部异常,而严重的呼吸困难使她不得不进行机械通气。放射影像学检查发现肺泡弥漫性浸润,与急性呼吸窘迫综合征(ARDS)一致。由于没有其他合理的病因,ARDS 被认为是继发于她的皮肤病。基因分析发现,编码 IL-36 受体拮抗剂的 IL36RN 发生了新型突变。迄今为止,仅有 15 例继发于银屑病的 ARDS 病例。这是已知的 IL36RN 基因突变携带者首次报告这种非常罕见的并发症。IL36RN在肺部和表皮中均有大量表达,这一事实可能是这一戏剧性病例不同寻常的临床特征的原因:本病例提示,需要仔细监测妊娠相关性泛发性脓疱型银屑病患者是否可能出现危及生命的肺部并发症,以及是否与 IL36RN 基因突变有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute Respiratory Distress Syndrome in a Carrier of an Interleukin-36 Receptor Antagonist Mutation With Generalized Pustular Psoriasis.

Background: Generalized pustular psoriasis of von Zumbusch is a rare variant of psoriasis often accompanied by systemic, sometimes life-threatening, symptoms. Generalized pustular psoriasis sometimes arises in pregnancy.

Case report: A 31-year-old female, with a history of schizophrenia and recurrent episodes of gestation-associated pustular psoriasis, was admitted to our department because of a generalized pustular rash during the 22nd week of her fifth pregnancy. Clinical and histopathological examinations were suggestive of generalized pustular psoriasis (von Zumbusch type). During this hospitalization, she developed acute dyspnea, fever, tachycardia, and marked leukocytosis. An extensive workup failed to reveal an infectious, cardiac, or pulmonary abnormality, while severe respiratory distress necessitated mechanical ventilation. Radio-imaging revealed diffuse alveolar infiltrates consistent with acute respiratory distress syndrome (ARDS). In the absence of any other plausible cause, ARDS was considered as secondary to her skin disease. Genetic base was suspected, and genetic analysis uncovered a novel mutation in IL36RN encoding the IL-36 receptor antagonist. Only 15 cases of ARDS secondary to psoriasis have been described to date. This is the first report of this very rare complication in a known carrier of an IL36RN mutation. The fact that IL36RN is abundantly expressed in the lung as well as in the epidermis may underlie the unusual clinical features of this dramatic case.

Conclusion: The present case suggests the need to carefully monitor patients with pregnancy-associated generalized pustular psoriasis for possible life-threatening pulmonary complications and the possible link to IL36RN mutation.

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CiteScore
1.30
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