免疫与生长的相互作用:一例合并可变免疫缺陷症和生长激素缺乏症的病例。

IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2024-09-30 eCollection Date: 2024-11-01 DOI:10.1097/MS9.0000000000002623
Sameer K Majety, Sagar Modh, Devrakshita Mishra, Nafisa Alam, Tarun K Suvvari, Chandra G M Pagadala, Gopichand Muppana
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引用次数: 0

摘要

导言:常见变异性免疫缺陷病(CVID)是临床上较常见的免疫缺陷病之一,病理复杂;而生长激素缺乏症(GHD)是一种以完全或相对缺乏人体生长激素为特征的疾病:本病例报告的患者是一名 13 岁女性,长期反复呼吸道感染和耳部感染,在其生命的第二个十年初期发育迟缓。诊断依据是针对 CVID 的血清免疫球蛋白彻底检查和针对 GHD 的促生长激素试验。为此,医生为患者量身定制了 IVIGs、促生长素治疗方案,并使用抗生素治疗反复感染:病例讨论:CVID 患者通常会反复出现呼吸道和耳部感染,免疫力明显下降。GHD通常在儿童时期被诊断出来,表现为生长发育迟缓和牙齿发育不良。在过去几十年中,免疫缺陷综合征与内分泌疾病并存的研究明显增多。本病例强调并讨论了将这两种病症联系在一起的复杂的潜在病理,同时也排除了各种差异:本报告强调了临床医生和患者在处理可能具有相对非特异性表现的双重健康问题时所面临的各种挑战。其中包括诊断困难、患者经济压力导致随访不力,以及从长远来看出现各种并发症。这就强调了早期疾病诊断和严格管理方案的重要性,以全面提高患者的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The interplay of immunity and growth: a case of combined variable immunodeficiency and growth hormone deficiency.

Introduction: Common variable immunodeficiency (CVID) is one of the more common immunodeficiencies seen in clinical practice with a complex disease pathology; while growth hormone deficiency (GHD) is a disorder characterized by complete or relative absence of the human growth hormone.

Case presentation: This case report presents a 13-year-old female patient with a long history of recurrent respiratory tract and ear infections, along with a notable failure to hit her developmental milestones early in the second decade of her life. The diagnosis was based on a thorough investigation of serum immunoglobulins for CVID and a GH stimulation test for GHD. For these, the patient was placed on a tailored regimen of IVIGs, somatropin therapy, and antibiotics for the recurrent infections.

Case discussion: CVID patients characteristically present with recurrent respiratory and ear infections, showing a marked decrease in immunity. Often diagnosed in childhood, GHD typically presents as growth failure along with developmental delays in dentition. There has been a notable rise in the coexistence of immunodeficiency syndromes and endocrinopathies studied in the past few decades. The case highlights and discusses the complex underlying pathology at play that links the two conditions to each other, while also excluding the various differentials.

Conclusion: The report highlights the various challenges faced by both clinicians and patients when dealing with dual health conditions that may have a relatively nonspecific presentation. Some of which include the diagnostic difficulties, financial strains on the patient leading to poor follow-up, and in the long-term, the development of various complications. This emphasizes the importance of early disease diagnosis and strict management protocols for the said disease, for the overall betterment of the patient's quality of life.

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Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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