scholarly journals A Rapidly Fatal Case of Lactobacillus Rhamnosus Sepsis Associated with Thyroid Storm in an Immunocompetent Patient

Author(s):  
Rita Dhar ◽  
Nasser Al-Rubai’aan ◽  
Wadha Alfouzan

We report a rapidly fatal case of 29-year-old man who presented with typical features of sepsis along with thyrotoxicosis. Presence of thrombotic lesions in his lower extremities led to the assumption that the source of infection could be endocarditis. However, transthoracic echocardiography did not confirm the preliminary diagnosis. Report of facultative anaerobic Gram-positive bacilli seen in the Gram stain of positive blood culture prompted initiation of treatment with ceftriaxone, vancomycin and metronidazole. Thyrotoxicosis was managed with propranolol, propylthiouracil, Lugol’s iodine and hydrocortisone. Diagnostic criteria for thyroid storm and infective endocarditis and therapy of Lactobacillus sepsis with a possible cause of death in the present case are discussed.

2018 ◽  
pp. bcr-2018-225265
Author(s):  
Mohd Shakirin Pairan ◽  
Nurashikin Mohammad ◽  
Sanihah Abdul Halim ◽  
Wan Syamimee Wan Ghazali

We present an interesting case of late-onset intracranial bleeding (ICB) as a complication of Streptococcus gordonii causing infective endocarditis. A previously healthy young woman was diagnosed with infective endocarditis. While she was already on treatment for 2 weeks, she had developed seizures with a localising neurological sign. An urgent non-contrasted CT brain showed massive left frontoparietal intraparenchymal bleeding. Although CT angiogram showed no evidence of active bleeding or contrast blush, massive ICB secondary to vascular complication of infective endocarditis was very likely. An urgent decompressive craniectomy with clot evacuation was done immediately to release the mass effect. She completed total 6 weeks of antibiotics and had postoperative uneventful hospital stay despite having a permanent global aphasia as a sequel of the ICB.


2020 ◽  
Vol In Press (In Press) ◽  
Author(s):  
Guive Sharifi ◽  
Mohammadreza Hajiesmaeili ◽  
Ilad Alavi Darazam ◽  
Maryam Haghighimorad ◽  
Muhanna Kazempour ◽  
...  

Introduction: Cerebral aspergillum is rare and usually misdiagnosed because its presentation mimics tuberculous meningitis, brain abscess, or tumor. The diagnosis and treatment of central nervous system (CNS) infections due to Aspergillus are very difficult because accurate diagnosis is often made intra-operatively. Case Presentation: Here, we report a case of cerebral aspergilloma in an immunocompetent host. A 35-year-old man admitted with progressive left hemifacial paresthesia followed by severe pain in trigeminal nerve territory. On physical examination, except for fifth nerve palsy and difficult mastication, there was not any sensory and motor deficit. Magnetic resonance imaging (MRI) of the brain showed T1 iso and T2 low signal lesion in the left parasellar region with enhancement. The lesion is extended to the left side of the prepontine cistern in the course of trigeminal nerve, craniotomy, and total surgical resection of the mass was performed. Isolated brain lesion and the pathology from stereotactic biopsy confirmed cerebral aspergillosis. The result of testing for human immunodeficiency virus (HIV) was negative. Although the patient had two subsequent recurrences, at first, good outcome was achieved by treatment with a combination of surgical intervention, and antifungal amphotericin B deoxycholate was administered, then changed to voriconazole. Unfortunately, after two years, he experienced new progressive symptoms, and the patient died despite several reoperations due to malfunctioning of external ventricle devices as well as the treatment of recurrent post-operation meningitis and voriconazole therapy. Conclusions: Most cases of intracranial aspergillosis show that this infection is pathogenic in immunocompromised hosts; however, in some cases, invasive Aspergillus was reported as an opportunistic infection in immunocompetent patients. In these patients, though primary cranial aspergillosis is very rare, it is possible that isolated brain involvement in a previously healthy case may be explained by unknown defects in immune pathways or massive exposure to spores.


Author(s):  
N. Sharma ◽  
M. Thalji ◽  
T. Chopade ◽  
A. Saini ◽  
A. Sharma ◽  
...  

CHEST Journal ◽  
2020 ◽  
Vol 158 (4) ◽  
pp. A470
Author(s):  
Fizza Hirani ◽  
Emily Zagorski ◽  
Marc Filstein ◽  
Rameez Phulphoto

2003 ◽  
Vol 36 (6) ◽  
pp. 697-704 ◽  
Author(s):  
Arthur J. Morris ◽  
Dragana Drinkovic ◽  
Sudha Pottumarthy ◽  
Marianne G. Strickett ◽  
Donald MacCulloch ◽  
...  

2018 ◽  
Vol 27 ◽  
pp. S592
Author(s):  
Van Truong ◽  
Rishendran Naidoo ◽  
Andrew Clarke ◽  
Vinod Sharma

Cureus ◽  
2020 ◽  
Author(s):  
Rony Shah ◽  
Linda C Klumpp ◽  
Nishant Nerella ◽  
Gustine Liu-Young ◽  
Jeffrey Jordan

2017 ◽  
Vol 7 (1) ◽  
pp. 63-66 ◽  
Author(s):  
Aijan Ukudeeva ◽  
◽  
Hal K. Hawkins ◽  
Masood Ahmad ◽  
Peerawut Deeprasertkul ◽  
...  

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