scholarly journals Staphylococcus pettenkoferiBacteremia: A Case Report and Review of the Literature

2015 ◽  
Vol 26 (6) ◽  
pp. 319-322 ◽  
Author(s):  
Abdulaziz Ahmed Hashi ◽  
Johannes Andries Delport ◽  
Sameer Elsayed ◽  
Michael Seth Silverman

Staphylococcus pettenkoferiis a relatively recently described coagulase-negative staphylococci species first described in 2002. Since then, nine additional cases of infection caused by this species have been reported in various countries around the world, including Germany, Belgium, France, South Korea, Italy, Brazil and Mexico. The present report describes a case ofS pettenkoferiperipheral line-associated bacteremia. To our knowledge, the present report is the first description of human infection caused byS pettenkoferiin Canada. The present report also provides an overview of the laboratory detection of uncommon coagulase-negative staphylococci.

1996 ◽  
Vol 110 (1) ◽  
pp. 52-56 ◽  
Author(s):  
Hidetoshi Haraguchi ◽  
Hitoshi Hentona ◽  
Hidekazu Tanaka ◽  
Atsushi Komatuzaki

AbstractPleomorphic adenoma arising in the external auditory canal is rare. We report the case of a 38-year-old man. To better grasp the clinical features and natural history of this uncommon tumour, we also reviewed the world wide literature and found 24 similar cases, which we analysed together with our own.


2015 ◽  
Vol 2015 ◽  
pp. 1-5
Author(s):  
Tiffany N. Latta ◽  
Aimee L. Mandapat ◽  
Joseph P. Myers

Spondylodiscitis caused byFusobacteriumspecies is rare. Most cases of spontaneous spondylodiscitis are caused byStaphylococcus aureusand most postoperative cases are caused byStaphylococcus aureusor coagulase-negative staphylococci.Escherichia coliis the most common Gram-negative organism causing spondylodiscitis.Fusobacteriumspecies are unusual causes for anaerobic spondylodiscitis. We report the case of a patient with spontaneous L2-L3 spondylodiscitis, vertebral osteomyelitis, and epidural abscess caused byFusobacteriumspecies and review the literature for patients withFusobacteriumspondylodiscitis.


Neurosurgery ◽  
1983 ◽  
Vol 13 (3) ◽  
pp. 322-326 ◽  
Author(s):  
Bruce Pendleton ◽  
Barton Carl ◽  
Michael Pollay

Abstract A lumbar spinal extradural ganglion cyst is reported, and the world literature on spinal ganglion cysts is reviewed. The clinical presentation, findings, etiology, and pathogenesis of these lesions are discussed.


Folia Medica ◽  
2021 ◽  
Vol 63 (2) ◽  
pp. 282-286
Author(s):  
Athena Myrou ◽  
Theodoros Aslanidis ◽  
Andreas Protopapas ◽  
Elisavet Psoma ◽  
Andreas Kontosis ◽  
...  

Though being usually a cutaneous tumor, melanomas can occur in several extracutaneous sites. Primary mucosal melanomas are rare, and primary gastric mucosal melanomas are considered extremely rare. Compared with cutaneous and ocular melanoma, mucosal melanomas have the lowest five-year survival. High level of suspicion of such rare condition may be the only way for early detection, diagnosis and chance for successful management of similar cases. In the present report, a case of a primary gastric melanoma in a 73-year-old man is described, along with a short review of the literature


2011 ◽  
Vol 53 (4) ◽  
pp. 219-222 ◽  
Author(s):  
José Luis Quirós ◽  
Ernesto Jiménez ◽  
Raúl Bonilla ◽  
Isabel Arce ◽  
Cristian Hernández ◽  
...  

Human abdominal angiostrongyliasis is a zoonotic disease caused by ingestion of the L3 larvae of Angiostrongylus costaricensis. The human infection gives rise to a pathological condition characterized by acute abdominal pain, secondary to an inflammatory granulomatous reaction, marked eosinophilia and eosinophilic vasculitis. Most commonly this disease is limited to intestinal location, primary ileocecal, affecting the mesenteric arterial branches and intestinal walls. We present one of the few cases reported around the world with simultaneous involvement of the intestines and liver, including proved presence of nematodes inside the hepatic arteriole.


2004 ◽  
Vol 128 (8) ◽  
pp. 922-925 ◽  
Author(s):  
Monica Garcia ◽  
Efren Buitrago ◽  
Pablo A. Bejarano ◽  
Javier Casillas

Abstract Liposarcoma is one of the most common neoplasms of adulthood. However, it is exceedingly rare in the gastrointestinal tract. To our knowledge, only 12 cases occurring in the esophagus have been reported in the world literature to date. We report the case of a 42-year-old man with a pleomorphic liposarcoma arising in the esophageal wall. The morphologic, immunophenotypic, and ultrastructural characteristics are presented, as well as the results of literature review.


2019 ◽  
Vol 11 (2) ◽  
pp. 157-165 ◽  
Author(s):  
Siriorn Udompanich ◽  
Kumutnart Chanprapaph ◽  
Poonkiat Suchonwanit

Linear and annular lupus panniculitis of the scalp (LALPS) is a unique subset of lupus panniculitis, which results in non-scarring alopecia along the Blaschko line of the scalp in an otherwise healthy young patient. Numerous cases have been reported around the world, but data on their trichoscopic findings and correlations with the underlying pathology is sparse. We hereby present a case of 23-year-old male with LALPS and further describe his trichoscopic findings as well as their correlations with histopathological features.


2017 ◽  
Vol 2017 ◽  
pp. 1-2 ◽  
Author(s):  
Murat Yasar Tas ◽  
Meral Merve Oguz ◽  
Mevlut Ceri

Acinetobacter lwoffii, a nonfermentative gram-negative aerobic bacillus, which presents in the normal flora of the oropharynx and skin, has recently been reported as a cause of human infection. Herein, the authors present a case report of peritonitis related to automated peritoneal dialysis caused by A. lwoffii.


2017 ◽  
Vol 2017 ◽  
pp. 1-5 ◽  
Author(s):  
Hussein Algahtani ◽  
Bader Shirah ◽  
Dina Abdulghani ◽  
Roiya Farhan ◽  
Raghad Algahtani

Brucellosis is a zoonotic bacterial infection which is transmitted to humans from infected animals and is endemic in many parts of the world including Saudi Arabia. In this article, we report a case of occupational neurobrucellosis that presented with a space-occupying lesion mimicking a brain tumor. We stress on the importance of obtaining detailed social history including occupation to reach the diagnosis in several conditions including brucellosis. We also stress on taking universal precautions when handling any specimens. It may be advisable that manipulation of all unknown specimens arriving at the laboratory should occur in biological safety cabinet until a highly infectious organism is ruled out. Neurobrucellosis should be included in the differential diagnosis in patients presenting with solitary mass lesion mimicking brain tumor especially in endemic areas or high occupational risk group.


2015 ◽  
Vol 2015 ◽  
pp. 1-4
Author(s):  
Daniela Hernández-Pérez ◽  
Claudia Butrón-Téllez Girón ◽  
Socorro Ruiz-Rodríguez ◽  
Arturo Garrocho-Rangel ◽  
Amaury Pozos-Guillén

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an uncommon inherited enzyme deficiency characterized by hemolytic anemia, caused by the inability of erythrocytes to detoxify oxidizing agents such as drugs, infectious diseases, or fava bean ingestion. In this later case, the disorder is known as favism. The aim of the present report was to present a review of the literature in this disease, to describe a case report concerning an affected 9-year-old male, and to review the main implications and precautions in pediatric dental management.


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