scholarly journals Leclercia adecarboxylataMusculoskeletal Infection in an Immune Competent Pediatric Patient: An Emerging Pathogen?

2015 ◽  
Vol 2015 ◽  
pp. 1-3 ◽  
Author(s):  
W. Jeffrey Grantham ◽  
Shawn S. Funk ◽  
Jonathan G. Schoenecker

Case. An immune competent pediatric patient presented with a persistent lower extremity infection withLeclercia adecarboxylataafter a penetrating injury. This case report details the presentation, clinical course, and treatment.Conclusion.Leclercia adecarboxylatahas increasing reports in immunosuppressed and adult patients with musculoskeletal infection. This case now indicates thatLeclercia adecarboxylatais a potential pathogen in immune competent children in musculoskeletal tissue.

2011 ◽  
Vol 57 (4) ◽  
pp. 25-27
Author(s):  
A I Sazonova ◽  
N V Molashenko ◽  
I S Iarovaia ◽  
N Iu Kalinchenko ◽  
E A Troshina

This case report illustrates peculiarities of the clinical course of congenital adrenal cortical dysfunction in adult patients presenting with the salt-losing form of the disease. Analysis of this case confirmed the necessity of dynamic observation of adults with this pathology in order to avoid complications that are likely to develop in case of inadequate treatment.


2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Catherine A. Gao ◽  
James M. Walter ◽  
Jane E. Dematte D’Amico

Abstract Background Adult patients with coronavirus disease present primarily with respiratory symptoms, but children and some adults may display a more systemic inflammatory syndrome with rash, fever, mucosal changes, and elevated inflammatory biomarkers. Case presentation Here, we report the case of a 29-year-old Hispanic patient presenting with significant rash and multisystem inflammation. We describe his clinical course, review dermatological manifestations of coronavirus disease, and summarize the pathophysiology of coronavirus disease-associated multisystem inflammation. Conclusion This case should alert physicians to the atypical nature of presenting rash with minimal respiratory symptoms in coronavirus disease.


2002 ◽  
Vol 29 (4) ◽  
pp. 387-389 ◽  
Author(s):  
Takeshi Tanaka ◽  
Masaharu Sudo ◽  
Koji Iwai ◽  
Shigeharu Fujieda ◽  
Hitoshi Saito

2013 ◽  
Vol 201 (2) ◽  
pp. 427-432 ◽  
Author(s):  
Zeyad A. Metwalli ◽  
J. Herman Kan ◽  
Karuna A. Munjal ◽  
Robert C. Orth ◽  
Wei Zhang ◽  
...  

2020 ◽  
Vol 110 (4) ◽  
Author(s):  
Juan Carlos Goez ◽  
Roger Lee Kilfoil ◽  
Chen-An Wang ◽  
Zachary Sax ◽  
Farzana Arif

Nail pathologies have a broad range of origin and may sometimes be complicated in presentation or clinical course, specifically when the pathology remains recalcitrant after treatment. In this case report we discuss a pathologic disorder that was initially misdiagnosed as a pyogenic granuloma surrounding an ingrown nail but was later found to be a benign neoplastic bone growth, Dupuytren exostosis, also known as a subungual exostosis. Operative treatment was deemed appropriate for the patient, and the exostosis was resected, leaving a soft-tissue void at the distal toe. The remaining void was filled with a perinatal graft, the use of which has been deemed effective anecdotally in both chronic and acute lower-extremity wounds but has not been widely discussed in the lower-extremity literature. This graft was placed to aid in wound healing over a potentially difficult wound bed. As amniotic, chorionic, and umbilical grafts become more prevalent in lower-extremity surgery, its antitumor effects should be further explored and published. This is the first case report, to our knowledge, of the successful use of a perinatal graft in the setting of a bone tumor, and it demonstrates that certain benign neoplasms can be treated with resection and placement of a perinatal graft while helping to prevent chronic wounds at surgical sites.


1996 ◽  
Vol 35 (2) ◽  
pp. 241
Author(s):  
Hak Soo Lee ◽  
Hyun Chul Rhim ◽  
Yong Soo Kim ◽  
Soon Young Song ◽  
Byung Hee Koh ◽  
...  
Keyword(s):  

2005 ◽  
Vol 8 (1) ◽  
pp. 23 ◽  
Author(s):  
Sanjay Kumar ◽  
Bharati Sinha

Chylopericardium after intrapericardial cardiac operations is extremely rare. We present an unusual case of postoperative chylopericardium with cardiac tamponade following atrial septal defect repair, and we comment on the clinical course and treatment.


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