scholarly journals Rothia mucilaginosus, an Uncommon Cause of Bacteremia in Immunocompromised Patients: Case Report and Literature Review

2008 ◽  
Vol 12 ◽  
pp. S37 ◽  
Author(s):  
Vicki Morrison ◽  
Shulasmith Bonham
2015 ◽  
Vol 2015 ◽  
pp. 1-5 ◽  
Author(s):  
Hao H. Nguyen ◽  
Nada Fadul ◽  
Muhammad S. Ashraf ◽  
Dawd S. Siraj

Mycobacterium marinum(M. marinum) is a ubiquitous waterborne organism that grows optimally at temperatures around 30°C. It is a nontuberculousMycobacteriumfound in nonchlorinated water with worldwide prevalence. It is the most common atypicalMycobacteriumthat causes opportunistic infection in humans.M. marinumcan cause superficial infections and localized invasive infections in humans, with the hands being the sites most frequently affected. It can cause skin lesions, which are either single, papulonodular lesions, confined to an extremity, or may resemble cutaneous sporotrichosis. This infection can also cause deeper infections including tenosynovitis, bursitis, arthritis, and osteomyelitis. Disseminated infections and visceral involvements have been reported in immunocompromised patients. We here report a case of severe deep soft tissue infection with necrotizing fasciitis and osteomyelitis of the left upper extremity (LUE) caused byM. marinumin an immunocompromised patient.


2018 ◽  
Vol 51 (3) ◽  
pp. 179-188 ◽  
Author(s):  
Malene Roed Spiegelhauer ◽  
Peter Fruergaard Andersen ◽  
Tove Havnhøj Frandsen ◽  
Rie Louise Møller Nordestgaard ◽  
Leif Percival Andersen

2021 ◽  
Vol 2021 ◽  
pp. 1-3
Author(s):  
Hemnishil K. Marella ◽  
Jiten P. Kothadia ◽  
Nasir Saleem ◽  
Bilal Ali ◽  
Yousef Abdel-Aziz ◽  
...  

Acute herpes simplex esophagitis (HSE) is common in immunocompromised patients. Eosinophilic esophagitis (EoE) is characterized by immune-mediated eosinophil-predominant esophageal inflammation. We report a patient with human immunodeficiency virus infection who presented with dysphagia and odynophagia and was found to have HSE and EoE. The combination of these two relatively rare conditions suggests possible predisposition.


2021 ◽  
Vol 108 (Supplement_6) ◽  
Author(s):  
N Glynn ◽  
S Martin ◽  
H Lewis

Abstract Aim This case report showcases an unusual presentation of tophaceous gout, in an immunocompromised patient. Furthermore, through a literature review, we highlight challenges posed by immunocompromised patients, the clinical manifestations of gout in the hand and principles of management. Method We report the case of a 62-year-old lady with previous liver transplant on immunosuppressants. She was admitted with a left palmar abscess, pyogenic tenosynovitis of the index finger and was taken to theatre for debridement and washout. Superimposed infection was apparent. This originated from an exophytic mass extending from the palm to FDS tendon insertion. This was debulked and histologically confirmed as gout. A review of the literature was performed using key search terms on PubMed relating to manifestations of gout in the tendons of the hand, and in patients on immunosuppression. Results Reports in the literature describe cases of gouty tendinopathy in both flexor and extensor tendons. Reported symptoms include triggering, tendon rupture and tenosynovitis. Gout occurs in a higher frequency in transplant patients. This can be attributed to medications such as cyclosporine which predispose to hyperuricaemia. Management of this condition involves medical optimisation. Despite concurrent problems with wound healing in the immunocompromised with gout, surgical intervention may be required. Indications include superimposed infection, attenuated tendon glide, joint movement, and neuropathy. Perioperative antibiotics are recommended in all immunocompromised patients. Conclusions This case highlights an unusual presentation of gout and the challenges of managing patients on immunosuppressant therapy. A greater awareness of this condition will allow for appropriate management in this high-risk patient cohort.


2009 ◽  
Author(s):  
C. L. Khoo ◽  
L. Regina ◽  
S. R. K. Naik ◽  
S. Kang

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