Clinical Evaluation and Outcomes of Mesenteric Lymphadenopathy in Children: A Cross-Sectional Analysis.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Medical Bulletin of Sisli Etfal Hospital Pub Date : 2025-03-18 eCollection Date: 2025-01-01 DOI:10.14744/SEMB.2025.59752
Bekir Yukcu, Zeynep Yildiz Yildirmak, Alper Ozel, Dildar Bahar Genc
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Abstract

Objectives: This study aimed to evaluate the etiology, clinical characteristics, and outcomes of mesenteric lymphadenopathy (ML) in children, with an emphasis on its clinical significance and management strategies.

Methods: This cross-sectional, single-center study was conducted between July 2016 and May 2017 and included pediatric patients aged 1 month to 18 years diagnosed with ML via abdominal ultrasonography. Patients with malignancies, acute infections, ongoing corticosteroid or antibiotic treatment, or incomplete follow-up were excluded. Data collection included demographic, clinical, and laboratory findings. Statistical analyses were performed using IBM SPSS Statistics version 25. The Mann-Whitney U test was used for comparisons of numerical variables between groups, while the chi-square and Fisher's exact tests were applied for categorical variables. A p-value less than 0.05 was considered statistically significant.

Results: A total of 106 patients were included with a median age of 7.4 years (range: 8 months-16.4 years), of whom 55.7% were male. The majority (63%) were aged 6-11 years. Abdominal pain was the most common symptom (64.2%), and 99.1% of the ML cases were localized in the right lower quadrant. At 1-month follow-up, lymph node sizes regressed to normal in 71.7% of cases, while 28.3% remained pathological. Antibiotic use did not significantly affect lymph node regression. At 6 months, no new symptoms or diagnoses were reported in the 91 patients contacted. ML was most often idiopathic (76.4%), with secondary causes including gastrointestinal and respiratory infections, acute abdomen, and Familial Mediterranean Fever.

Conclusion: In children, ML is predominantly benign and self-limiting, and in most cases, it resolves without medical intervention. Although its association with symptoms such as abdominal pain may cause anxiety in parents, careful monitoring of patients can prevent unnecessary interventions. This study underscored the importance of conservative management and highlighted the need for further research with larger cohorts and extended follow-up periods to explore rare etiologies and long-term outcomes.

儿童肠系膜淋巴结病的临床评价和预后:横断面分析。
目的:本研究旨在评价儿童肠系膜淋巴结病(ML)的病因、临床特点和转归,重点探讨其临床意义和治疗策略。方法:本横断面单中心研究于2016年7月至2017年5月进行,纳入1个月至18岁的通过腹部超声诊断为ML的儿科患者。排除恶性肿瘤、急性感染、正在进行皮质类固醇或抗生素治疗或随访不完全的患者。数据收集包括人口统计、临床和实验室结果。采用IBM SPSS Statistics version 25进行统计分析。数值变量组间比较采用Mann-Whitney U检验,分类变量组间比较采用卡方检验和Fisher精确检验。p值小于0.05被认为具有统计学意义。结果:共纳入106例患者,中位年龄7.4岁(范围:8个月~ 16.4岁),其中55.7%为男性。大多数(63%)年龄在6-11岁之间。腹痛是最常见的症状(64.2%),99.1%的ML病例局限于右下腹。在1个月的随访中,71.7%的病例淋巴结大小恢复正常,28.3%的病例保持病理状态。抗生素使用对淋巴结消退无显著影响。在6个月时,91名接触的患者没有报告新的症状或诊断。ML通常是特发性的(76.4%),继发原因包括胃肠道和呼吸道感染、急性腹部和家族性地中海热。结论:在儿童中,ML主要是良性和自限性的,并且在大多数情况下,无需药物干预即可解决。尽管它与腹痛等症状有关,可能会引起父母的焦虑,但对患者的仔细监测可以防止不必要的干预。该研究强调了保守治疗的重要性,并强调需要进一步研究更大的队列和延长随访期,以探索罕见的病因和长期结果。
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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来源期刊
Medical Bulletin of Sisli Etfal Hospital
Medical Bulletin of Sisli Etfal Hospital MEDICINE, GENERAL & INTERNAL-
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16.70%
发文量
41
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