[Chronic non-bacterial osteomyelitis with autoimmune hepatitis: a case report and literature review].

M Jin, X M Zhong, Y C Yan, K Y Yao, J M Lai
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Abstract

Objective: To summarize the clinical characteristics and treatments of chronic non-bacterial osteomyelitis with autoimmune hepatitis in children. Methods: A child who had chronic non-bacterial osteomyelitis with autoimmune hepatitis was admitted to the Department of Gastroenterology of the Children's Hospital Capital Institute of Pediatrics at April 2022. The clinical data was retrospectively analyzed. Using the keywords of "chronic non-bacterial osteomyelitis""autoimmune hepatitis" in Chinese and English, the literature from database establishment to December 2022 in CNKI, Wanfang, China Biomedical Literature Database and Pubmed was searched. Combined with this case, the clinical characteristics and treatment of chronic non-bacterial osteomyelitis combined with autoimmune hepatitis were analyzed. Results: A 5 years and 3 months girl was admitted to the Department of Gastroenterology of Children's Hospital, Capital Institute of Pediatrics for "transaminase elevated for 1 year and swelling of right maxillofacial area for half a year". The physical examinations at admission found a 4.0 cm × 4.0 cm swelling area with tenderness before the right ear, abdominal distention with visible abdominal wall vein, firm and enlarged liver (10.0 cm below the xiphoid and 4.5 cm below the right ribs), and splenomegaly (Line Ⅰ 10.0 cm, Line Ⅱ 11.5 cm, and Line Ⅲ 25.0 cm). There was no redness, swelling or restriction of the limbs. Laboratory examination found abnormal liver function with alanine aminotransferase 118 U/L, aspartate aminotransferase 227 U/L, γ-glutamyltransferase 360 U/L, and positive direct anti-human globulin test; immunology test found immunoglobulin G 41.60 g/L and a homogeneous type of antinuclear antibody of 1∶1 000; the autoimmune hepatitis antibody test found a positive anti-smooth muscle antibody (1∶100). Liver biopsy showed moderate interfacial inflammation and the patient was diagnosed with autoimmune hepatitis (International Autoimmune Hepatitis Group 19). The imaging findings showed extensive involvement of the bilateral mandible, while the right side was severe. There were expansile bone changes, thinning of the bone cortex, and significant swelling of the surrounding soft tissue in the mandibular body, mandibular angle, and mandibular ramus. After treatment of glucocorticoid, the swelling of the right maxillofacial region disappeared and the transaminase returned to normal. Only one case was reported before in English and none in Chinese. The two cases were both girls whose main clinical features were joint pain and swelling. The previous case started with pain in both knee joints, and developed liver injury during treatment while this case had liver injury as the initial clinical presentation. Besides, the affected sites and degrees of arthritis in the 2 cases were different. After glucocorticoid treatment, the clinical symptoms were alleviated, and transaminases returned to normal. Conclusions: Chronic non bacterial osteomyelitis may involve the liver and manifest as autoimmune hepatitis. Glucocorticoids therapy is effective.
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慢性非细菌性骨髓炎合并自身免疫性肝炎1例报告并文献复习。
目的:总结儿童慢性非细菌性骨髓炎合并自身免疫性肝炎的临床特点及治疗方法。方法:2022年4月,首都儿科研究所儿童医院消化内科收治1例慢性非细菌性骨髓炎合并自身免疫性肝炎患儿。回顾性分析临床资料。以中文和英文“慢性非细菌性骨髓炎”“自身免疫性肝炎”为关键词,检索CNKI、万方、中国生物医学文献数据库和Pubmed数据库自建库至2022年12月的文献。结合该病例,分析慢性非细菌性骨髓炎合并自身免疫性肝炎的临床特点及治疗方法。结果:1例5岁零3个月女童因“转氨酶升高1年,右侧颌面部肿胀半年”入住首都儿科研究所儿童医院消化内科。入院体检发现右耳前肿胀区4.0 cm × 4.0 cm,有压痛,腹胀可见腹壁静脉,肝脏紧实肿大(剑突下方10.0 cm,右肋下方4.5 cm),脾肿大(Ⅰ10.0 cm,Ⅱ11.5 cm,Ⅲ25.0 cm)。四肢没有发红、肿胀或受限。实验室检查发现肝功能异常,丙氨酸转氨酶118 U/L,天冬氨酸转氨酶227 U/L, γ-谷氨酰转氨酶360 U/L,直接抗人球蛋白试验阳性;免疫学检查发现免疫球蛋白G为41.60 G /L,抗核抗体为1∶1 000均质型;自身免疫性肝炎抗体试验抗平滑肌抗体阳性(1∶100)。肝活检显示中度界面炎症,诊断为自身免疫性肝炎(国际自身免疫性肝炎第19组)。影像学结果显示双侧下颌骨广泛受累,而右侧严重。骨膨胀性改变,骨皮质变薄,下颌体、下颌角、下颌支周围软组织明显肿胀。经糖皮质激素治疗后,右颌面部肿胀消失,转氨酶恢复正常。此前英文报告1例,中文报告无一例。两例均为女童,主要临床特征为关节疼痛和肿胀。前一例患者以双膝关节疼痛为首发症状,在治疗过程中出现肝损伤,而本例患者的首发临床表现为肝损伤。此外,2例患者患关节炎的部位和程度不同。经糖皮质激素治疗后,临床症状减轻,转氨酶恢复正常。结论:慢性非细菌性骨髓炎可累及肝脏,表现为自身免疫性肝炎。糖皮质激素治疗是有效的。
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