Imunodeficiência comum variável associada à doença de Crohn-like: relato de caso e revisão da literatura

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL
Larissa Cristina Tavares de Castro, Z. Calamita
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引用次数: 0

Abstract

AIMS: To report the case of a patient diagnosed with common variable immunodeficiency and Crohn-like disease, describing the clinical picture, the diagnostic investigation process, the therapeutic approaches and the clinical outcome of the patient. To carry out a literature review of case reports addressing patients with the common variable immunodeficiency and Crohn-like disease association. Emphasize the importance of early diagnosis and treatment.CASE DESCRIPTION: A male patient was diagnosed with common variable immunodeficiency at nine years of age and with non-specific inflammatory bowel disease at 10 years, after colonoscopy and colonic biopsy indicated moderate lymphoplasmacytic, eosinophilic infiltrate and some neutrophils in lamina propria, with absence of granulomas. At age 14, the diagnosis of Crohn-like disease was confirmed by specialist after correlation between clinical history and complementary exams. Currently with 18 years of age, the patient is under treatment with intravenous human immunoglobulin, infliximab and azathioprine, with stabilization of the clinical picture.CONCLUSIONS: The literature review identified 11 case reports on the association between common variable immunodeficiency and Crohn-like disease, with no Brazilian studies, which highlights the rarity of such association. In this report, the patient received extensive and empirical treatments due to the difficulty in reaching a specific diagnosis, which was only performed at age 14, when more targeted and individualized treatment was started. Although currently stable, the patient presented several complications during the diagnostic investigation, which emphasizes the importance of early diagnosis and more precise treatment, targeted to meet the health needs of these patients.
与克罗恩病相关的常见免疫缺陷病毒:病例报告和文献综述
目的:报告一例被诊断为常见可变免疫缺陷和克罗恩样疾病的患者,描述患者的临床情况、诊断调查过程、治疗方法和临床结果。对涉及常见可变免疫缺陷和克罗恩病相关患者的病例报告进行文献综述。强调早期诊断和治疗的重要性。病例描述:一名男性患者在9岁时被诊断为常见可变免疫缺陷,在10岁时被确诊为非特异性炎症性肠病,结肠镜检查和结肠活检显示固有层有中度淋巴浆细胞、嗜酸性粒细胞浸润和一些中性粒细胞,无肉芽肿。在14岁时,通过临床病史和补充检查之间的相关性,专家确认了克罗恩样疾病的诊断。该患者目前18岁,正在接受静脉注射人类免疫球蛋白、英夫利昔单抗和硫唑嘌呤的治疗,临床情况稳定。结论:文献综述确定了11例关于常见变异性免疫缺陷与克罗恩病之间相关性的病例报告,但没有巴西的研究,这突出了这种相关性的罕见性。在本报告中,由于难以得出具体诊断,患者接受了广泛的经验治疗,而这一诊断仅在14岁时进行,当时开始了更有针对性和个性化的治疗。尽管目前病情稳定,但患者在诊断调查中出现了一些并发症,强调了早期诊断和更精确治疗的重要性,旨在满足这些患者的健康需求。
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来源期刊
Scientia Medica
Scientia Medica MEDICINE, GENERAL & INTERNAL-
CiteScore
0.70
自引率
20.00%
发文量
14
审稿时长
10 weeks
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