Jarkoc Tarik, Cengic Adisa, Selmanovic Velma, Hadzimuratovic Amila, Vukas Emina, Uzicanin Sajra, Huseinbegovic Zinka, Sarajlic Mirna
Pediatric Clinic, Clinical Center University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
Mater Sociomed. 2025;37(2):106-110. doi: 10.5455/msm.2025.37.106-110.
Benign acute childhood myositis (BACM) is a rare complication of viral URTIs, usually occurring in winter. It is characterized by acute onset of bilateral calf pain and difficulty/refusal to walk. A prodromal phase precedes these manifestations, consisting of catarrhal and constitutional symptoms. These are associated with increased muscle-specific enzymes, usually normal inflammatory parameters, and leukopenia.
Our study aimed to define the demographic, clinical, and laboratory characteristics of BACM patients and determine the etiology leading to their development.
Medical charts for patients diagnosed with BACM from October to April 2023/2024 at the Pediatric Clinic Clinical Center University of Sarajevo, Department of Allergology, Rheumatology, and Immunology were reviewed retrospectively. Relevant medical information was collected for 20 patients. Statistical analysis was done in Microsoft Excel 2013.
Demographic analysis demonstrated male predominance (75%), with primarily school-aged children affected (median age 8.36). Most cases occurred in winter (60%). The majority of patients presented with bilateral calf pain (100%), difficulty walking (90%), and fever (100%). All cases demonstrated increased CK levels, with median values of 3779 U/L; a notable number had leukopenia (70%). The most commonly isolated pathogen was Influenza B virus (75%).
BACM is relatively rare but presents acutely and leads to plenty of distress for both patients and their parents. A child with coryzal symptoms complicated by bilateral calf pain or difficulty/refusal to walk and an increase in CK levels should raise suspicion of BACM. The condition is self-limiting and usually resolves without complications.
儿童良性急性肌炎(BACM)是病毒性上呼吸道感染(URTIs)的一种罕见并发症,通常发生在冬季。其特征为双侧小腿疼痛急性发作,以及行走困难/不愿行走。在这些表现出现之前有一个前驱期,包括卡他症状和全身症状。这些症状与肌肉特异性酶升高、通常正常的炎症参数以及白细胞减少有关。
我们的研究旨在确定BACM患者的人口统计学、临床和实验室特征,并确定导致其发病的病因。
回顾性分析2023年10月至2024年4月在萨拉热窝大学临床中心儿科诊所过敏、风湿病和免疫学系诊断为BACM的患者的病历。收集了20例患者的相关医学信息。在Microsoft Excel 2013中进行统计分析。
人口统计学分析显示男性占优势(75%),主要影响学龄儿童(中位年龄8.36岁)。大多数病例发生在冬季(60%)。大多数患者表现为双侧小腿疼痛(100%)、行走困难(90%)和发热(100%)。所有病例的肌酸激酶(CK)水平均升高,中位值为3779 U/L;相当数量的患者有白细胞减少(70%)。最常分离出的病原体是乙型流感病毒(75%)。
BACM相对罕见,但起病急,给患者及其父母带来诸多困扰。出现卡他症状并伴有双侧小腿疼痛或行走困难/不愿行走且CK水平升高的儿童应怀疑患有BACM。该病具有自限性,通常无需并发症即可痊愈。