Abdominal mass hiding rib osteomyelitis

Genny Raffaeli, Irene Borzani, Raffaella Pinzani, Caterina Giannitto, Nicola Principi, Susanna Esposito

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Background: Rib osteomyelitis is a rare entity, occurring in approximately 1 % or less of all cases of haematogenous osteomyelitis. Given its rarity and clinical heterogeneity, the diagnosis of rib osteomyelitis can be challenging and requires a high index of suspicion. We present a case of acute osteomyelitis of the rib due to community-acquired methicillin-resistant Staphylococcus aureus (MRSA), which occurred in an otherwise healthy 3-month-old infant and mimicked an epigastric hernia at first. Case presentation: An otherwise healthy 3-month-old female infant was sent by her primary care paediatrician to the paediatric emergency department for possible incarcerated epigastric hernia because for 2 days, she had suffered from mild to moderate fever, irritability, poor feeding, and tender epigastric swelling. Ultrasonographic imaging excluded epigastric hernia, and transthoracic echocardiography ruled out endocarditis. However, clinical assessment combined with laboratory criteria classified the child into the high-risk group for having severe bacterial infection. Consequently, awaiting the definitive diagnosis, she was immediately treated with a broad-spectrum regimen of intravenous antibiotic therapy based on vancomycin (40 mg/kg/die in 3 doses) and meropenem (100 mg/kg/die in 3 doses). Three days after admission, the blood culture result was positive for methicillin-resistant Staphylococcus aureus, and vancomycin remained as antibiotic therapy. On day 3, a second swelling appeared at the level of the seventh left rib, 2 cm-wide, non-erythematous, mildly painful. Ultrasonography of the left chest wall on this occasion showed an image consistent with an acute osteomyelitis of the anterior osteo-chondral region of the 7th rib and associated adjacent periosteal and soft tissue collection and magnetic resonance imaging confirmed the osteomyelitis of the anterior middle-distal part of the 7th left rib, near the costochondral junction. Vancomycin was continued up to a total of 6 weeks of therapy, and at the end, the child was discharged in good condition with no relapse during the follow-up. Conclusion: This is one of the few reported cases of paediatric rib osteomyelitis caused by community-acquired MRSA. Timely identification associated with prompt and targeted antibiotic therapy may allow full recovery.

Original languageEnglish
Article number251
JournalItalian Journal of Pediatrics
Volume42
Issue number1
DOIs
Publication statusPublished - Apr 12 2016

Fingerprint

Ribs
Osteomyelitis
Vancomycin
Methicillin-Resistant Staphylococcus aureus
Hernia
meropenem
Anti-Bacterial Agents
Pediatrics
Thoracic Wall
Therapeutics
Endocarditis
Bacterial Infections
Cartilage
Echocardiography
Hospital Emergency Service
Ultrasonography
Primary Health Care
Fever
Magnetic Resonance Imaging
Recurrence

Keywords

  • Bone infection
  • MRSA
  • Osteomyelitis
  • Rib
  • Staphylococcus aureus

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Abdominal mass hiding rib osteomyelitis. / Raffaeli, Genny; Borzani, Irene; Pinzani, Raffaella; Giannitto, Caterina; Principi, Nicola; Esposito, Susanna.

In: Italian Journal of Pediatrics, Vol. 42, No. 1, 251, 12.04.2016.

Research output: Contribution to journalArticle

Raffaeli, Genny ; Borzani, Irene ; Pinzani, Raffaella ; Giannitto, Caterina ; Principi, Nicola ; Esposito, Susanna. / Abdominal mass hiding rib osteomyelitis. In: Italian Journal of Pediatrics. 2016 ; Vol. 42, No. 1.
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