Group A Beta-Haemolytic Streptococcal Necrotising Fasciitis: Early Diagnosis and Clinical Features

Dermatology ◽  
2004 ◽  
Vol 208 (1) ◽  
pp. 5-9 ◽  
Author(s):  
T. Simonart
The Lancet ◽  
1994 ◽  
Vol 344 (8930) ◽  
pp. 1111-1115 ◽  
Author(s):  
J. Chelsom ◽  
A. Halstensen ◽  
J. Chelsom ◽  
T. Haga ◽  
E.A. Høiby

2020 ◽  
Vol 16 ◽  
Author(s):  
Molla Imaduddin Ahmed ◽  
Rosalind V Saunders ◽  
Srini Bandi

: We reviewed the clinical presentation and management of children with Invasive group A streptococcal infections admitted to our tertiary Children’s Hospital in the last eight years. Our study highlighted the varied symptomatology and management practices in children with iGAS and showed that early diagnosis and prompt initiation of appropriate antibiotics for iGAS can help in resolution of symptoms and good outcome.


2020 ◽  
Vol 13 (12) ◽  
pp. e236800
Author(s):  
Grace Anne McCabe ◽  
Thomas Hardy ◽  
Thomas Gordon Campbell

A previously independent 56-year-old immunocompetent woman presented with septic shock in the setting of periorbital swelling and diffuse infiltrates on chest imaging. Blood cultures were positive for growth of group A Streptococcus (GAS). Broad spectrum antimicrobials were initiated with the inclusion of the antitoxin agent clindamycin. Necrosis of periorbital tissue was noted and surgical consultation was obtained. Débridement of both eyelids with skin grafting was performed. GAS was isolated from wound cultures and also observed on periorbital tissue microscopy. The final diagnosis was bilateral periorbital necrotising fasciitis (PONF) associated with invasive GAS infection. The patient had a prolonged intensive care unit course with input from multiple specialist teams. This case demonstrates the importance of early recognition and treatment of PONF, the profound systemic morbidity caused by these infections, and illustrates successful multidisciplinary teamwork.


1998 ◽  
Vol 16 (3) ◽  
pp. 403-407 ◽  
Author(s):  
David B Drake ◽  
Julia A Woods ◽  
Timothy J Bill ◽  
Bradley W Kesser ◽  
Mark A Wenger ◽  
...  

1994 ◽  
Vol 28 (3) ◽  
pp. 359 ◽  
Author(s):  
Julia Chelsom ◽  
Alfred Halstensen ◽  
Tore Haga ◽  
Arne Høiby

PEDIATRICS ◽  
1977 ◽  
Vol 60 (6) ◽  
pp. 935-937
Author(s):  
David W. McCandless ◽  
William E. Hodgkin

Subacute necrotizing encephalomyelopathy (SNE) was first described in 1951 by Denis Leigh.1 Since then, well over 100 cases have been described, and probably as many as 100 more have been diagnosed (at postmortem examination) and not recorded. With an increased awareness of the clinical features of this disease comes an increase in early diagnosis. Such diagnosis is not easy, however, since there is a broad range of variability in symptoms and time of onset. Characteristically, most patients with SNE develop normally until about 1 year of age. the parents may note a gradual reduction in development. There is usually a loss of appetite with resultant weight loss.


2011 ◽  
Vol 17 (3) ◽  
pp. 358-364 ◽  
Author(s):  
B.R. Kittang ◽  
T. Bruun ◽  
N. Langeland ◽  
H. Mylvaganam ◽  
M. Glambek ◽  
...  

2013 ◽  
Vol 33 (3) ◽  
pp. 227-229
Author(s):  
Raashid Hamid ◽  
Sajad A Wani ◽  
AH Shera ◽  
Sheikh Khurshid ◽  
NA Bhat ◽  
...  

Meckel’s Diverticulum (MD) is a frequent congenital anomaly of small bowel often difficult to diagnose. It is usually asymptomatic and can present as bleeding, obstruction and inflammation. We report a case of MD in a 3 year old male child, diagnosed by 99mTc pertechnetate scan and confirmed on laparotomy. Excised specimen revealed a large MD with multiple ileal ulcers, as a source of massive bleeding per rectum. The clinical features and need for early diagnosis and treatment are discussed. DOI: http://dx.doi.org/10.3126/jnps.v33i3.7802   J. Nepal Paediatr. Soc. 2013;33(3):227-229


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