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Case Challenge A 10-Week-Old Female with Fever and an Inability to Move Her Left Leg Bilge Aldemir-Kocabas, MD; Adem Karbuz, MD; Suat Fitöz, MD; Ergin Çiftçi, MD; and Erdal Ince, MD Bilge Aldemir-Kocabaş, MD, is a Fellow, Division of Pediatric Infectious Diseases, Department of Pediatrics, School of Medicine, Ankara University. Adem Karbuz, MD, is a Fellow, Division of Pediatric Infectious Diseases, Department of Pediatrics, School of Medicine, Ankara University. Suat Fitöz, MD, is a Professor, Department of Radiology, School of Medicine, Ankara University. Ergin Çiftçi, MD, is a Professor, Division of Pediatric Infectious Diseases, Department of Pediatrics, School of Medicine, Ankara University. Erdal İnce, MD, is a Professor, Division of Pediatric Infectious Diseases, Department of Pediatrics, School of Medicine, Ankara University. Address correspondence to Bilge AldemirKocabaş, MD, Division of Pediatric Infectious Diseases, Department of Pediatrics, School of Medicine, Ankara University, TR-06590 Cebeci, Ankara, Turkey; email: [email protected]. Disclosure: The authors have no relevant financial relationships to disclose. doi: 10.3928/00904481-20141022-06 Figure 1. Magnetic resonance images showing signal hyperintensity and contrast enhancement (arrows) in the left quadriceps muscle group on the (A) coronal and (B) axial axes. A previously healthy 10-weekold female was admitted to our hospital with a fever and an inability to move her left leg. The mother also noted a decrease in the child’s breast-feeding in the 3 days prior to presentation. Although there was no history of major trauma, it was revealed that her brother had picked her up roughly by her leg 5 days before her admission. On initial physical examination, she had increased capillary refill and tachycardia with toxic appearance. Flexion-adduction and internal rotation posture, and warmth, tenderness, and limitation of movement of the left hip joint were detected. Her laboratory findings were as follows: white blood cell count of 11700/mm3, erythrocyte sedimentation rate of 87 mm/h, and C-reactive protein level of 86 mg/L. For diagnosis, see page 443 Editor’s note: Each month, this department features a discussion of an unusual diagnosis. A description and images are presented, followed by the diagnosis and an explanation of how the diagnosis was determined. As always, your comments are welcome via email at [email protected]. 442 Copyright © SLACK Incorporated Case Challenge Diagnosis: Pyomyositis Caused by Streptococcus pneumoniae The diagnoses of soft tissue infection and septic shock were established. Fluid replacement therapy was given to the patient immediately. After a blood culture was taken, intravenous ceftriaxone at a dose of 75 mg/kg/d was initiated. A heterogeneous appearance on the left quadriceps muscle group was detected sonographically. Pathological signal change, contrast enhancement, and myositis of the left quadriceps muscle group were identified by magnetic resonance imaging (Figure 1). The blood culture was positive for Streptococcus pneumoniae. Her fever resolved and limitation of abduction of the hip joint gradually improved at follow-up. Ceftriaxone treatment was continued for a total of 10 days, after which she was discharged from the hospital. Sonographic findings and physical examination were completely normal at the end of the first month of follow-up. The pneumococcal serotype was typed as S. pneumoniae serotype 5 according to polymerase chain reaction (PCR) assays. DISCUSSION Pyomyositis (PM) is a rare infection of the muscle tissue that occurs most often in childhood. Striated muscle is actually resistant to microorganism invasion. The most common cause of PM is Staphylococcus aureus. It is suggested that trauma is a facilitating factor for microorganism invasion in patients with PM,1-5 but trauma has been reported in only about 10% of PM patients (in our case there was a possibility of accidental trauma caused by the patient’s brother). Thus, invasion of pneumococci to the hip muscle might be facilitated by this event during the bacteremia caused by S. pneumoniae. PEDIATRIC ANNALS • Vol. 43, No. 11, 2014 A number of risk factors have been identified for the development of pneumococcal infections and related complications such as PM. These include age (older than 65 years or younger than 2 years), chronic heart, lung, kidney, and liver diseases; diabetes mellitus; cerebrospinal fluid leaks; cochlear implants; some hematological diseases and malignancies; functional or anatomic asplenia; HIV infection; use of immunosuppressive drugs (including steroids); and solid organ transplantation or hypocomplementemia.5-7 In an at-risk group, gram-negative enteric organisms, anaerobes, and fungi also can be causative pathogens for PM. Diagnosis of PM requires both radiologic evidence and positive culture of blood, muscle aspirate, or other fluid. PM can be classified into three stages. In the early stage, treatment with antibiotics alone can be effective for controlling local infection and does not require surgery.5 Osteomyelitis, septic arthritis, fever of unknown origin, cellulitis, thrombophlebitis, and appendicitis should be kept in mind in the differential diagnosis of PM.1 Also, PM should be considered in the differential diagnosis of septic-appearing children as well as children complaining of joint pain or muscle pain.2 Our 10-week-old infant had received a 13-valent pneumococcal conjugate vaccine (PCV-13) 15 days before admission (PCV13 includes type 5). The incidence of invasive pneumococcal diseases in children younger than age 5 years has decreased dramatically with routine use of PCV.8 Bacteremia without a known site of infection is the most common invasive clinical presentation of pneumococcal infection among children age 2 years and younger, and it accounts for approximately 70% of invasive diseases in this age group. Before routine use of PCV, the burden of pneumococcal diseases among children younger than age 5 years was significant.8,9 Complete immune response requires at least three dosages of vaccine. Due to insuf- ficient maturity of the immune system in infancy and lack of a full dose of pneumococcal vaccination, infants are more prone to invasive pneumococcal infections. In conclusion, PM should be considered in the differential diagnosis of pain and restriction in movement of the hip joint in a child, especially in a child with a toxic appearance. Moreover, PM should also be kept in mind if a child with pneumococcal bacteremia has pain and limitation of hip joint on physical examination, and a child with these symptoms should be evaluated immediately with imaging techniques. REFERENCES 1.Zadroga RJ, Zylla D, Cawcutt K, et al. Pneumococcal pyomyositis: report of 2 cases and review of the literature. Clin Infect Dis. 2012;55(3):1217. 2. Taksande A, Vilhekar K, Gupta S. Primary pyomyositis in a child. Int J Infect Dis. 2009;13(4):149-151. 3.Bertrand SL, Lincoln ED, Prohaska MG. Primary pyomyositis of the pelvis in children: a retrospective review of 8 cases. Orthopedics. 2011;34(12):832-840. 4.Kern L, Rassbach C, Ottolini M. Streptococcal pyomyositis of the psoas: case reports and review. Pediatr Emerg Care. 2006;22(4):250-253. 5.Chen MC, Yang SH, Yao TK, Chong PN, Chen SH. Bilateral hip pain caused by adductor pyomyositis as the initial presentation of chronic myeloid leukemia in a 17-year-old child. Pediatr Neonatol. 2011;52(6):353-357. 6.Ekdahl K, Truedsson L, Sjoholm AG, Braconier JH. Complement analysis in adult patients with a history of bacteremic pneumococcal infections or recurrent pneumonia. Scand J Infect Dis. 1995;27(2):111-117. 7.Dee TH, Schiffman G, Sottile MI, Rytel MW. Immunologic studies in pneumococcal disease. J Lab Clin Med. 1977;89(6):1198-1207. 8.American Academy of Pediatrics. Pneumococcal infections. In: Pickering LK, Baker CJ, Kimberlin DW, Long SS, eds. Red Book: 2012 Report of the Committee on Infectious Diseases. 29th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2012:571-582. 9.Nuorti JP, Whitney CG; Centers for Disease Control and Prevention (CDC). Pneumococcal Disease. Prevention of pneumococcal disease among infants and children - use of 13-valent pneumococcal conjugate vaccine and 23-valent pneumococcal polysaccharide vaccine - recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep. 2010;59(RR-11):1-18. 443