scholarly journals Spinal abscess in a patient with undiagnosed gerbode defect: a case report

Author(s):  
Y W Liao ◽  
B Ensam ◽  
A Kodamanchile ◽  
S Duckett

Abstract Background Gerbode defect is a rare cardiac defect in which an abnormal communication occurs between the left ventricle and right atrium. The aetiology is usually congenital but acquired defects can occur. Case summary We report on a 47-year-old male with atrioventricular block prior to decompression of an epidural abscess extending from the skull base to the seventh thoracic vertebrae. Following positive blood cultures for Staphylococcus Aureus, a transoesophageal echocardiogram performed revealed a small Gerbode defect with associated endocarditis. In our case, the defect was small and there was no evidence of heart failure, there was little guidance or literature available on how to best manage our patient. A multidisciplinary decision was taken to treat the endocarditis medically and to not close the defect in the acute setting. He recovered well and did not suffer any further cardiac complications. A repeat transthoracic echocardiogram did not reveal any evidence of endocarditis. Conclusion Gerbode defects are rare but have been known to increase the risk of developing endocarditis. It is important to have a high clinical suspicion of endocarditis in patients with evidence of conduction disorders and systemic infection.

2019 ◽  
Vol 5 (3) ◽  
pp. 103-106
Author(s):  
Mohammad Reza Hasanjani Roushan ◽  
Soheil Ebrahimpour ◽  
Zeinab Mohseni Afshar ◽  
Arefeh Babazadeh

Abstract Introduction Human brucellosis, the most prevalent zoonotic disease worldwide, is a systemic infection which can involve several organs. Among musculoskeletal complaints, spondylitis is the most frequent complication of brucellosis and primarily affects the lumbar and thoracic vertebrae. The involvement of the cervical spine is infrequent. Case report This case report concerns an unusual case of cervical spine spondylitis with an epidural abscess due to Brucella in a 43-year-old man. The diagnosis was based on the patient being domiciled in an endemic region, his symptoms and his occupation. Clinical outcomes improved following antimicrobial therapy of rifampin, doxycycline, and gentamycin, and were confirmed radiologically. Conclusion Early diagnosis and treatment are crucial for these patients. The timely commencement of medical treatment can help prevent surgery.


2021 ◽  
Vol 5 (2) ◽  
Author(s):  
Nicholas Sunderland ◽  
Ahmed El-Medany ◽  
Justin Temporal ◽  
Laura Pannell ◽  
Gemina Doolub ◽  
...  

Abstract Background  The Gerbode defect is a rare abnormal communication between the left ventricle (LV) and right atrium (RA). The lesion is either congenital or acquired. Acquired defects are largely iatrogenic or infective in origin. We present two cases of acquired Gerbode defects with similar clinical presentations but very different outcomes. Case summaries Patient 1 A 64-year-old male presented with features of decompensated cardiac failure and a low-grade temperature. Dehiscence of a recently implanted bioprosthetic aortic valve and high-velocity LV to RA jet (Gerbode defect) was found on echocardiography. Blood cultures grew Staphylococcus warneri and the diagnosis of infective endocarditis was established. The patient was treated with intravenous antibiotics and the aortic valve and Gerbode defect were successfully surgically repaired. Patient 2 An 81-year-old male presented after being found on the floor at home. On admission, he was clinically septic with evidence of decompensated heart failure. No clear infective focus was initially found. Transthoracic echocardiography revealed severe left ventricular impairment, with a normal bioprosthetic aortic valve. He was treated with intravenous antibiotics, but later deteriorated with evidence of embolic phenomena. Repeat echocardiography revealed a complex infective aortic root lesion with bioprosthetic valve dehiscence and flow demonstrated from the LV to RA. Unfortunately, the patient succumbed to the infection and cardiac complications. Discussion  The Gerbode defect is a rare but important complication of infective endocarditis and valve surgery. Care needs to be taken to assess for Gerbode defect shunts on echocardiogram, especially in the context of previous cardiac surgery.


Folia Medica ◽  
2016 ◽  
Vol 58 (4) ◽  
pp. 289-292 ◽  
Author(s):  
Hatice Reşorlu ◽  
Suzan Saçar ◽  
Beşir Şahin Inceer ◽  
Ayla Akbal ◽  
Ferhat Gökmen ◽  
...  

AbstractBrucellosis is a zoonotic disease widely seen in endemic regions and that can lead to systemic involvement. The musculoskeletal system is frequently affected, and the disease can exhibit clinical involvements such as arthritis, spondylitis, spondylodiscitis, osteomyelitis, tenosynovitis and bursitis. Spondylitis and spondylodiscitis, common complications of brucellosis, predominantly affect the lumbar and thoracic vertebrae.Epidural abscess may occur as a rare complication of spondylitis. Spinal brucellosis and development of epidural abscess in the cervical region are rare. Development of epidural abscess affects the duration and success of treatment. Spinal brucellosis should be considered in patients presenting with fever and lower back-neck pain in endemic regions, and treatment must be initiated with early diagnosis in order to prevent potential complications.


2010 ◽  
Vol 21 (1) ◽  
pp. e75-e78 ◽  
Author(s):  
Colin B Josephson ◽  
Saleh Al-Azri ◽  
Daniel J Smyth ◽  
David Haase ◽  
B Lynn Johnston

Intravesical Bacillus Calmette-Guérin (BCG) immunotherapy is an accepted treatment for transitional cell carcinoma of the bladder. Carcinoma in situ of the bladder progresses to invasive muscular disease in approximately 54% of untreated patients, mandating early initiation of therapy once the diagnosis is confirmed. Should BCG treatment fail, an additional course of BCG combined with interferon-alpha, both administered intravesically, is a promising second-line immunotherapy. In greater than 95% of patients, BCG is tolerated without significant morbidity or mortality. However, both early (within three months of the original treatment) and late presentations of systemic infection resulting from intravesical BCG treatment have been described. The present study describes the course of a 75-year-old man with a late presentation of BCG vertebral osteomyelitis, discitis, epidural abscess, bilateral psoas abscesses and probable cerebral tuberculoma, following treatment regimens of intravesical BCG followed by intravesical BCG plus interferon-alpha 2b.


Author(s):  
Aditi Sharma ◽  
Thilipan Thaventhiran ◽  
Suzanne Braggins ◽  
Channa N Jayasena ◽  
Vassiliki Bravis

Summary Infection is a common complication of advanced diabetic foot disease, increasing the risk of acute admission and amputation. It is less well-known that foot ulceration and osteomyelitis may cause bacteraemia-associated hematogenous seeding and subsequent epidural abscess formation. Here we describe the case of a 57-year-old woman with known diabetic foot ulcer with underlying osteomyelitis admitted with backpain in the absence of trauma. Her condition deteriorated secondary to overwhelming sepsis. MRI of the spine confirmed spondylodiscitis and posterior epidural collection, not amenable to surgical intervention due to patient’s comorbidities and high surgical risk. Despite prolonged antibiotic therapy, the patient died following a hospital admission lasting 2.5 months. This case highlights the importance of regular contact with diabetes foot service for optimisation and prompt treatment of diabetic foot disease, which can be an underestimated potential source of remote site invasive systemic infection. Secondly, high clinical suspicion in admitting clinicians is imperative in ensuring timely diagnosis and early intervention to minimise fatal consequences. Learning points Approximately 10% of patients with diabetes will develop a foot ulcer in their lifetime. Spondylodiscitis (incorporating vertebral osteomyelitis, spondylitis and discitis) is a rare condition and diabetes is the most common predisposing risk factor. Spondylodiscitis often presents with no other symptom other than back pain. Neurological or infective symptoms can be present or absent. High clinical suspicion in clinicians is imperative in ensuring timely diagnosis and early intervention to minimise devastating consequences.


2019 ◽  
Vol 1 (1) ◽  
pp. 2-10
Author(s):  
Andy Wijayanto ◽  
◽  
Nunuk Muktiati ◽  
Farhad Bal'afif ◽  
Sri Rianawati ◽  
...  

Background: Tuberculosis is an infectious disease that develop from systemic infection caused by bacterium Mycobacterium tuberculosis complex. Generally, M.tuberculosis spread from one person to another through nuclear droplet air transmission. Although TB has a lower transmission rate compared to another infectious disease, TB still become a global health problem. It is estimated that approximately one third of the world’s population is infected by tuberculosis. Every year it is estimated that there are nine million new cases and close to two million death cases caused by tuberculosis. Case: A 24-year-old female was admitted to the hospital complaining of could not move both of her legs and could not urinate. One month before admission, she was diagnosed with meningitis TB; miliary TB; and meningioma at thoracic vertebrae T11-12 based on physical examination, laboratory examination, Chest X-Ray, Head CT Scan without contrast, and thoracolumbal MRI. When admitted to the hospital, the patient already treated with Fixed Dose Combination of antituberculosis Drugs first category for one and a half month from Turen Primary Healthcare. Then the patient underwent bronchoscopy examination. The result of the anatomical pathology examination showed class two. Then the patient underwent a laminectomy surgery and tumor excision at thoracic vertebrae T11-12. The result of postoperative Anatomical Pathology examination showed a neurofibroma pattern. After surgery, the Physical Medicine and Rehabilitation Department placed thoracic lumbosacral orthoses (TLSO) to the patient. Postoperative evaluation up to three months showed that the patient’s general condition was quite good but still cannot move both of her legs and cannot urinate.


Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 2793-2793
Author(s):  
Ranjan Pathak ◽  
Madan Raj Aryal ◽  
Smith Giri ◽  
Paras Karmacharya ◽  
Anthony A Donato

Abstract Background Thrombotic thrombocytopenic Purpura (TTP) has been reported to be associated with serious cardiac complications including arrhythmia, sudden cardiac death, myocardial infarction, cardiogenic shock, and heart failure. These complications are believed to be the sequelae of diffuse platelet thrombi leading to infarction in cardiac tissue. However, the true burden of cardiac complications in TTP in clinical practice remains unclear. Methods We used the 2009-2011 Nationwide Inpatient Sample database to identify hospitalizations in patients ≥18 years with a diagnosis of TTP (International Classification of Diseases, 9th revision, Clinical Modification [ICD-9-CM] code 446.6. Nationwide Inpatient Sample is the largest all-payer publicly available inpatient care database in the US. It contains data from five to eight million hospital stays from about 1,000 hospitals across the country and approximates a 20% sample of all US hospitals. ICD-9-CM codes were used to identify any of the following coded cardiac complications- 1) arrhythmias, 2) acute myocardial infarction (MI), 3) cardiogenic shock, 4) acute heart failure, and 5) conduction abnormalities. Univariate and multivariate logistic regression was used to determine the odds of various cardiac complications in patients with TTP compared to patients without TTP. Univariate analysis was done to compare baseline demographic and hospital characteristics between patients among TTP patients with and without cardiac complications. Data analysis was done using STATA version 13.0 (College Station, TX). Results Of the estimated total 4,367 TTP hospitalizations, 22.2 % (n=969) developed at least 1 of the above cardiac complications. Mean age of our cohort was 56.2±17.3, with the majority of patients being white (55.1%). Compared to those with TTP and no reported cardiac events, dyslipidemia (p=0.01) hypertension (p=0.001), peripheral vascular disease (p=0.03), acute kidney injury (p<0.001), chronic kidney disease (p=0.003), stroke (p=0.01), sepsis (p=0.01) and coronary artery disease (p<0.001) were more likely in patients with cardiac complications (Table 1). On multivariate analysis, patients with TTP were found to develop acute MI more commonly than patients without TTP (OR 5.22, 95% CI 3.81-7.15; p<0.001). Interestingly, acute heart failure was found to be less common in TTP patients (OR 0.7, 95% CI 0.55-0.90; p=0.002). There was no significant difference in the incidence of arrhythmias, cardiogenic shock and conduction disorders among patients with TTP compared to patient without TTP (Figure 1). Conclusion In this study of large national database, acute MI was found to be the most common cardiac complication in patients with TTP. Although reported, arrhythmias, cardiogenic shock and conduction disorders were not significantly associated with TTP. Table Characteristic TTP without Cardiac Complications (n=3,398) TTP with Cardiac Complications (n=969) p Age, mean ± SD 44.5±15.2 56.2±17.3 <0.001 Sex 0.094 Male 31.3 38.7 Female 68.7 61.3 Race 0.009 White 41.8 55.1 Black 45.1 33.5 Hispanic 8.3 4 Asian or Pacific Islander 1.1 3.5 Native American 0.7 0.6 Other 3 3.3 Primary Payer <0.001 Medicare 18.9 37.8 Medicaid 23.9 14.9 Private insurance 42.4 37.4 Self-pay 10.1 5 No charge 0.7 2 Other 4 2.9 Region 0.520 Northeast 15.6 18.2 Midwest 26.7 27.9 South 45.6 39.5 West 12.1 14.4 Comorbidities Smoking 26.8 26.2 0.871 Obesity 12.1 9.1 0.210 Dyslipidemia 13.2 21.9 0.009 Hypertension 50.3 62.9 0.001 DM 23.5 27.9 0.227 PVD 1.1 4.4 0.029 CAD 5.1 15.4 <0.001 AKI 35.5 61.1 <0.001 CKD 16.5 27.3 0.003 Stroke 4.9 11.8 0.007 Sepsis 3.9 9.7 0.01 AKI = Acute Kidney Injury; CAD = Coronary Artery Disease; CKD = Chronic Kidney Disease; DM = Diabetes Mellitus; PVD = Peripheral Vascular Disease Figure 1. Multivariate analysis of Cardiac Complications in TTP Figure 1. Multivariate analysis of Cardiac Complications in TTP Disclosures No relevant conflicts of interest to declare.


Author(s):  
Younes A ◽  
◽  
Yalamanchili S ◽  
Ali H ◽  
Onyekwelu C ◽  
...  

Chagas disease is a systemic infection due to Trypanosoma cruzi, a parasitic protozoan. Trypanosoma cruzi is endemic in Latin America; however, the prevalence has been increasing in the United States. The infection is mostly vector-borne secondary to triatomine or “kissing” bug bites. However, the infection can also spread via organ transplantation, blood transfusion, or transplacentally resulting in congenital manifestations. Chronic Chagas disease can cause cardiac or gastrointestinal complications that may be irreversible if left untreated. Major cardiac complications include dilated cardiomyopathy, arrhythmias, sudden cardiac death, and thromboembolism.


2020 ◽  
Vol 4 (2) ◽  
pp. 01-03
Author(s):  
Lindsey Tilling

Background Hydroxychloroquine (HCQ) is a 4-aminoquinoline derivative, used in the treatment of malaria and rheumatic diseases. HCQ has also been suggested as a treatment in patients suffering from severe acute respiratory syndrome–coronavirus 2 (SARS–CoV-2). One of the cardiac complications of SARS-CoV-2 is myocarditis and ventricular dysfunction. Case summary We present the case of a 52 year old lady presenting with 2 months history of breathlessness, found to have severely impaired left ventricular function. She had been taking HCQ for 28 months for seronegative inflammatory arthritis. No cause was identified on initial investigation. She was treated with optimal medical therapy, and HCQ was stopped. After 5 months a cardiac MRI scan revealed full remodelling of the ventricle. Discussion This case highlights one of the lesser recognized side effects of HCQ, and the potential for severe cardiac dysfunction. As this drug continues to be investigated and used in the management of SARS-CoV-2 it is important to recognize the potential for cardiac decompensation in patients who are already at increased risk of myocardial dysfunction.


2021 ◽  
Vol 5 (1) ◽  
Author(s):  
Anne Sofie Frederiksen ◽  
Steen Hylgaard Jørgensen ◽  
Henrik Wiggers ◽  
Ellen-Margrethe Hauge

Abstract Background Extra-articular manifestations (EAMs) are common in patients with rheumatoid arthritis (RA). Cardiac EAMs are rare but may cause complete heart block and damage to the heart valves. Case summary We present the case of a middle-aged woman with long-standing RA and EAMs as the most prominent symptoms. The patient experienced complete atrioventricular heart block and developed nodular vegetations affecting the mitral valve, ultimately leading to severe mitral regurgitation and valve replacement. Discussion The diagnosis of cardiac EAMs in RA may be challenging for the clinicians. Symptoms and findings may mimic more common conditions such as malignancy and infectious endocarditis. A multidisciplinary approach is of paramount importance in order to make an early diagnosis and to provide optimal treatment to patients with RA and cardiac complications.


Sign in / Sign up

Export Citation Format

Share Document