[Necrotizing pneumonia in a patient with selective IgA deficiency].

María Enriqueta Núnez-Núñez, Denisse Monraz-Monteón, Juan Carlos Lona-Reyes, Luis Iván Pozos-Ochoa, Diego Magallón-Picazo, Beatriz Bayardo-Gutierrez
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Abstract

Background: Inborn errors of immunity originate from monogenic mutations that should be considered in the suggestive diagnosis of patients with recurrent or severe infections, allergies, autoimmunity, autoinflammatory diseases, bone marrow failure and malignancy.

Case report: Pediatric patient, male, 4 years old, treated in the medical service for fever of 39°C, difficult to control. The simple chest x-ray reported left pulmonary consolidation. The infectious condition evolved into necrotizing pneumonia of the left upper lobe, so it was decided to perform a lobectomy. The diagnosis of some inborn error of immunity was suspected. The determination of serum immunoglobulins reported IgA below the reference values. At 4 years he continued to have decreased serum IgA (5.5 mg/dL).

Conclusions: The diagnosis of selective IgA deficiency is established after 4 years of life; However, due to the patient's severe infection, addressing some inborn error of immunity had to be implemented.

[选择性IgA缺乏患者的坏死性肺炎]。
背景:先天性免疫错误源于单基因突变,在反复或严重感染、过敏、自身免疫、自身炎症性疾病、骨髓衰竭和恶性肿瘤患者的暗暗性诊断中应予以考虑。病例报告:小儿患者,男,4岁,因发热39℃,难以控制而就诊。单纯胸片示左肺实变。感染状况演变为左上叶坏死性肺炎,因此决定进行肺叶切除术。怀疑某些先天性免疫错误的诊断。血清免疫球蛋白测定报告IgA低于参考值。4年后,他的血清IgA继续下降(5.5 mg/dL)。结论:选择性IgA缺乏症的诊断在4岁后确立;然而,由于患者感染严重,必须解决一些先天性免疫错误。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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