$$\rightleftharpoonup{xx}$$
$$\longleftharp{xx}$$,
$$\longrightharp{xx}$$,
Sternoclavicular joint infection (SCJI) is a rare form of septic arthritis, accounting for less than 1% of all infectious arthritis cases1,2. Despite its low incidence, SCJI can lead to serious complications such as mediastinitis, chest wall abscess, and pulmonary empyema2,3,4. Staphylococcus capitis, a coagulase-negative staphylococcus (CoNS) and a common commensal organism of human skin, has been increasingly implicated in catheter-related bloodstream infections, prosthetic joint infections, and wound infections5,6,7. However, SCJI caused by Staphylococcus capitis has been rarely reported in the literature8. Common risk factors for SCJI include diabetes mellitus, immunosuppression, and a history of intravenous drug use2,9,10. Nonetheless, cases have also been reported in healthy individuals without underlying conditions11,12,13. While Staphylococcus capitis is generally regarded as a benign skin colonizer, it can act as an opportunistic pathogen under specific conditions5.
This case report describes a sternoclavicular joint infection caused by Staphylococcus capitis in a patient who presented primarily with chest tightness and palpitations. The diagnosis was ultimately established through imaging studies and microbiological examinations, confirming a Staphylococcus capitis–associated sternoclavicular joint infection. The patient underwent surgical debridement followed by a total of 10 weeks of antibiotic therapy, resulting in complete resolution of the infection. This case is clinically relevant and appropriate for reporting because it involves a typical high-risk population (elderly, diabetic, and history of malignancy) with an atypical initial presentation, thereby filling a key knowledge gap regarding S. capitis-induced SCJI. This report aims to increase clinicians' awareness of sternoclavicular joint infections caused by Staphylococcus capitis and highlights the importance of early diagnosis and individualized treatment strategies14,15,16.
CASE PRESENTATION:
A 74-year-old female patient presented to the First Affiliated Hospital of Zhejiang University with a chief complaint of palpitations and chest tightness that had persisted for half a day. The symptoms began suddenly while the patient was riding an elevator, characterized by palpitations, chest oppression, and shortness of breath. She denied dizziness, blurred vision, chest pain, or other discomfort. The patient had a 5-year history of type 2 diabetes, managed with metformin (two tablets daily), and a history of right-sided breast cancer, for which she underwent a radical mastectomy 20 years ago.
Upon admission, physical examination revealed the following: Temperature: 37.2 °C; Pulse: 78 beats/min; Respiratory rate: 19 breaths/min; Blood pressure: 128/79 mmHg. The patient was alert, oriented, and had a normal mental status. A reddish-purple mass, approximately 2 cm in diameter, was observed at the right sternoclavicular joint. The mass was soft, with localized skin warmth and purulent bloody discharge. No jaundice was noted in the skin or sclera. Pupils were equal and reactive to light. Lung auscultation was clear without rales, and the heart rhythm was regular with no pathological murmurs. The abdomen was soft, non-tender, and without rebound pain. No lower limb edema was observed, and muscle strength and tone were normal in all extremities, with no movement limitation.
Laboratory Investigations showed the following: white blood cells (WBC): 6.43 × 109/L; Neutrophils: 67.8%; C-reactive protein (CRP): 51.47 mg/L (normal < 6.00 mg/L); electrocardiogram (ECG): Supraventricular tachycardia (heart rate > 200 beats/min); Mycobacterium tuberculosis PCR polymerase chain reaction (PCR) assay of infected tissue: Negative.
Abdominal CT scan showed no acute abdominal pathology. Ultrasound revealed a mixed cystic-solid mass in the right subclavicular region, suggestive of inflammation. The MRI of the chest wall (3.0 T) showed an occupying lesion at the anterior edge of the right proximal clavicle and sternoclavicular joint, with recommended contrast-enhanced imaging. Inflammatory exudates were observed in the right chest wall, upper arm subcutaneous tissues, and fascial planes. Enlarged lymph nodes were noted in the left axilla and mediastinum. A preliminary diagnosis of skin infection involving the right sternoclavicular joint was made, and the patient was admitted for further treatment.
The patient received preoperative intravenous ertapenem (1.0 g/day) and surgical debridement of the infected lesion was performed. Intraoperatively, two purulent abscesses were identified at the right sternoclavicular joint, along with localized purulent sinus tracts and necrosis of both the fascia and bone. Intraoperative observation confirmed that the stability of the sternoclavicular joint was preserved and not compromised by infection or debridement. The procedure involved excising necrotic tissue, debriding osteomyelitic and necrotic fascia, and inflammatory subcutaneous tissue. The wound was irrigated, and hemostasis was achieved. The flap was closed, and two negative-pressure drainage tubes were placed.
Postoperative diagnosis confirmed clavicular osteomyelitis. The pus drainage was sent for culture and bacterial identification, which revealed Staphylococcus capitis, sensitive to ertapenem. The patient continued on ertapenem (1.0 g IV daily) and received supportive treatments, including pain management, gastric protection, and nutritional support. Inflammatory markers decreased rapidly postoperatively, with CRP levels dropping from 51.47 mg/L to 17.38 mg/L within 4 weeks.
The patient successfully completed a 10-week course of antibiotic therapy, consisting of 2 weeks of intravenous ertapenem, followed by 8 weeks of oral linezolid. No adverse drug reactions or complications were noted during the treatment. At 1-month follow-up, the wound had healed well, and the patient's symptoms had significantly improved, with complete resolution of palpitations, chest tightness, and dyspnea.
Diagnosis, Assessment, and Plan:
The patient was diagnosed with a rare primary sternoclavicular joint infection complicated by osteomyelitis, initially suspected clinically and radiologically as a bacterial pyogenic infection. Surgical exploration confirmed purulent material, necrotic soft tissue, and osteomyelitis involving the medial clavicle. The patient is an elderly female with multiple risk factors, including long‑standing diabetes and a history of malignant tumor, which predisposed her to opportunistic infection. Clinical presentation was atypical, with chest tightness and palpitations as chief complaints, while local inflammatory signs and elevated inflammatory markers supported an active infectious process. Imaging confirmed deep soft tissue and bone involvement, and microbiological culture identified Staphylococcus capitis as the causative pathogen. The treatment plan included urgent surgical debridement of necrotic bone and soft tissue, targeted antibiotic therapy based on culture results, and soft tissue reconstruction with a pedicled myofascial flap to achieve durable wound closure. Antibiotic therapy consisted of 2 weeks of intravenous ertapenem followed by 8 weeks of oral linezolid, with close monitoring of inflammatory markers and wound healing. Postoperative follow‑up was scheduled to assess healing, infection resolution, and potential recurrence. Long‑term management includes regular outpatient review, wound care education, and instruction regarding warning signs of recurrent infection.