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一名因STAT1功能缺失变异和原发性免疫缺陷病而患多灶性骨髓炎的儿童发生播散性卡介苗感染,经抗结核治疗后显著改善:病例报告

Disseminated BCG infection in a child with multifocal osteomyelitis due to STAT1 LOF variant and primary immunodeficiency disease was significantly improved after anti-tuberculosis treatment: a case report.

作者信息

Ouyang Haiping, Yang Di, Wang Zhongliang

机构信息

Department of Orthopedics Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key, Laboratory of Child Development and Disorders, Chongqing Municipal Health Commission Key Laboratory of Children's Vital Organ Development and Diseases, Chongqing, China.

出版信息

Front Pediatr. 2025 Sep 5;13:1626146. doi: 10.3389/fped.2025.1626146. eCollection 2025.

Abstract

BACKGROUND

This was a rare case where the diagnosis was not obvious during treatment, but the treatment was effective after diagnosis. An infant with recurrent fever was considered for systemic multiple osteomyelitis after two surgical biopsies. After a third operation to take a lymph node biopsy, the patient was finally diagnosed as having disseminated Bacille Calmette-Guerin(BCG) disease caused by BCG vaccination. After diagnosis, the child was effectively treated with anti-tuberculosis therapy.

CASE DESCRIPTION

A 2-month-old female patient was hospitalized twice for fever and surface mass. The patient underwent a puncture biopsy of the right tibia and a puncture biopsy of the lesion of the right leg respectively. The patient was diagnosed with systemic multiple osteomyelitis. The patient still had recurrent fever after antibiotic treatment. At outpatient follow-up, the patient was found to have primary immunodeficiency disease with STAT1 LOF mutation. When the child was one year and one month old, she was hospitalized again with a fever. The patient underwent a third operation, a biopsy of the left axillary lymph node. The pathological results suggested granulomatous inflammation, which was considered tuberculosis. The child was diagnosed with disseminated BCG vaccine disease. After 16 months of oral treatment with isoniazid, rifampicin, ethambutol,and levofloxacin, the child's condition was significantly improved.

CONCLUSIONS

The performance of multiple surgical biopsies is crucial in cases of infants presenting with recurrent fever and widespread bone destruction, as well as in children diagnosed with primary immunodeficiency disease, particularly when the available etiological tests offer limited diagnostic evidence.

摘要

背景

这是一例在治疗过程中诊断不明确,但确诊后治疗有效的罕见病例。一名反复发热的婴儿在两次手术活检后被考虑为全身性多发性骨髓炎。在进行第三次手术取淋巴结活检后,患者最终被诊断为卡介苗接种引起的播散性卡介苗病。确诊后,患儿接受抗结核治疗,病情得到有效控制。

病例描述

一名2个月大的女性患者因发热和体表肿物两次住院。患者分别接受了右胫骨穿刺活检和右腿肿物穿刺活检,被诊断为全身性多发性骨髓炎。抗生素治疗后患者仍反复发热。门诊随访时,发现患者患有STAT1基因功能缺失突变的原发性免疫缺陷病。患儿1岁1个月时因发热再次住院,接受了第三次手术,即左腋窝淋巴结活检。病理结果提示肉芽肿性炎症,考虑为结核。患儿被诊断为播散性卡介苗病。经异烟肼、利福平、乙胺丁醇和左氧氟沙星口服治疗16个月后,患儿病情明显改善。

结论

对于出现反复发热和广泛骨质破坏的婴儿,以及诊断为原发性免疫缺陷病的儿童,尤其是在现有病因学检查提供的诊断证据有限时,多次手术活检至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/12446307/ec9d99cffaa5/fped-13-1626146-g001.jpg

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