Infective endocarditis with Osler’s nodule in a patient with Osler’s disease: a case report and review of the literature

Background Hereditary hemorrhagic telangiectasia, also known as Osler–Weber–Rendu disease, induces arteriovenous malformations in visceral organs. Arteriovenous malformations increase the risk of severe infections and are a common complication associated with hemorrhagic telangiectasia. However, cases of endocarditis associated with hemorrhagic telangiectasia are rarely reported. Although hemorrhagic telangiectasia causes erythematous macules on the extremities, these macules are usually painless. We encountered a rare case of infective endocarditis in a patient with Osler–Weber–Rendu disease. Case presentation A 52-year-old Japanese woman who was diagnosed with hemorrhagic telangiectasia 5 years prior presented to our hospital with fever and muscular pain. She had erythematous nodules and tenderness on the finger, heel, and toe, suggestive of Osler’s nodes. A physical examination revealed tachycardia with a 3/6 pansystolic murmur. A transesophageal echocardiogram showed vegetations along the atrial side of the mitral valve and mild mitral regurgitation because of prolapse of the anterior commissure. Methicillin-sensitive Staphylococcus aureus was identified in the blood cultures. Detection of distinctive skin lesions, so-called Osler’s nodes, was the symptomatic key to early diagnosis, and the patient was treated without surgery. She was discharged with negative blood cultures after a 6-week intravenous antibiotic administration. Conclusions Our report highlights the importance of considering the risk of extracerebral infections including endocarditis in hemorrhagic telangiectasia. This rare case effectively demonstrates the importance of proper diagnosis of skin lesions.


Background
Hereditary hemorrhagic telangiectasia (HHT) or Osler-Weber-Rendu disease (Osler's disease) is an autosomal dominant disorder characterized by vascular anomalies that may visually develop in many organs [1]. Two main types of HHT represent 80% of cases: HHT type 1 results from mutations in the encoding for the endoglin (ENG) gene, while HHT type 2 results from mutations in the activin type II-like receptor kinase 1 (ACVRL1) gene (encoding for the activin receptor-like kinase). The ENG and ACVRL1 genes code for proteins of the TGFbeta receptor, which is involved in proper blood vessel development [2]. Four main clinical diagnostic criteria have been established and carefully delineated for HHT: epistaxis, telangiectasia, visceral lesions, and an appropriate family history [3]. Diagnosis of HHT is confirmed when any three of the given criteria are presented.

Open Access
*Correspondence: takawata-cardio@gifu-u.ac.jp Vascular anomalies in visceral organs include cerebral, spinal, hepatic, pancreatic, and pulmonary arteriovenous malformations (AVMs). These AVMs allow for direct communication between pulmonary and systemic circulation and expose patients with HHT to increased risk of severe infections. Although numerous cases of severe infections, such as cerebral abscesses, septicemia, arthritis, and osteomyelitis, have been reported, cases of endocarditis associated with HHT are relatively rare [4][5][6][7]. Here, we present a case of infective endocarditis in a patient with HHT.
Electrocardiography showed sinus tachycardia (heart rate, 110 beats/minute) with no significant arrhythmia or changes in the ST segment. Radiographic examinations, including chest radiography and computed tomography, revealed no significant findings suggestive of infection. Transthoracic echocardiography (TTE) showed left ventricular ejection fraction of 66%, and mild mitral regurgitation was observed. As TTE could not confirm the presence or absence of vegetation because of a poor echo image, transesophageal echocardiography (TEE) was performed. TEE revealed vegetation along the atrial side of the mitral valve and the anterior commissure prolapse of the mitral valve (Fig. 2). There were no findings in the TEE suggestive of a perivalvular abscess.
Blood cultures were drawn, and intravenous ceftriaxone (2 g every 12 hour) was administered. Methicillin-sensitive Staphylococcus aureus was subsequently identified in the blood cultures. Magnetic resonance imaging of the brain revealed multiple cerebral infarctions suggestive of septic emboli. After initiation of antibiotic treatment, repeat blood cultures drawn on day 3 were negative.
The patient was discharged with negative blood cultures after 6 weeks of intravenous antibiotic administration. Thereafter, she has been followed up regularly in the outpatient clinic and is progressing well with no recurrence signs.

Discussion and conclusions
HHT causes vascular abnormalities and, therefore, is considered to be a risk factor for developing cerebral infections. Additionally, numerous recent reports have described the risk of severe extracerebral infections Fig. 1 Osler's node (arrowhead) on the right ring finger (a), right heel (b), and fifth toe (c) associated with HHT. A retrospective analysis of 353 patients with HHT reported that 47 patients (13.6%) were affected by severe infection [7]. Among them, extracerebral infections accounted for 67% of all infections, and approximately 20% of them were caused by Staphylococcus aureus.
Several reports have proposed possible mechanisms of extracerebral infections in patients with HHT. Duval et al. [6] hypothesized that severe extracerebral infection complicating HHT is related to bacterial invasion of the nasal mucosa because of cotton packing. Guilhem et al. [8] reported that patients with HHT exhibit immunological abnormalities including T CD4, T CD8, and NK cell lymphopenia and increased levels of immunoglobulins G and A.
Despite the high risk of developing severe bacterial infections, infective endocarditis associated with HHT is relatively rare. To our knowledge, there are only eight cases of infective endocarditis in patients with HHT [9][10][11][12][13][14][15][16]. Among them, only two cases were treated medically without valvular surgery (Table 1). Our study is the third case report of infective endocarditis, successfully treated only with antibiotics. In addition to chest auscultation, skin examination is important for early diagnosis of infective endocarditis. Although HHT itself causes erythematous macules on the extremities, these macules are usually painless. Detection of erythematous nodules with tenderness (Osler's nodes) in this case was the symptomatic key finding that indicated infective endocarditis. Interestingly, Osler's disease and Osler's node were named after Sir William Osler. Both are known for their characteristic skin abnormalities; however, in this case, we could properly distinguish them based on whether they were painful. Moreover, early diagnosis based on this skin finding in our patient may have allowed for treatment without surgical intervention.
In conclusion, we encountered a rare case of infective endocarditis in a patient with HHT. Recognizing the risk  of extracerebral infections, including endocarditis, in patients with HHT is important for early diagnosis and for providing appropriate patient care. This rare case effectively demonstrates the importance of proper diagnosis of skin lesions, which leads to early diagnosis that can prevent progression of infective endocarditis and achieve good clinical course without invasive treatment.