Recurrent neutrophilic dermatosis of the face associated with aortitis syndrome: A case report.

1988 ◽  
Vol 50 (4) ◽  
pp. 650-656 ◽  
Author(s):  
Noriyuki MISAGO ◽  
Hiromu KOHDA
Head & Neck ◽  
1994 ◽  
Vol 16 (1) ◽  
pp. 75-78 ◽  
Author(s):  
Thiam Chye Lim ◽  
Walter Tiang Lee Tan ◽  
Yoke Sun Lee

2010 ◽  
Vol 163 (3) ◽  
pp. 638-640 ◽  
Author(s):  
T. Agostini ◽  
C. Catelani ◽  
A. Acocella ◽  
A. Franchi ◽  
R. Bertolai ◽  
...  

2014 ◽  
Vol 41 (7) ◽  
pp. 661-662 ◽  
Author(s):  
Takahiro Arita ◽  
Tomoko Nomiyama ◽  
Jun Asai ◽  
Hideya Takenaka ◽  
Miyuki Fukuoka ◽  
...  

1994 ◽  
Vol 34 (12) ◽  
pp. 821-824 ◽  
Author(s):  
Shinjitsu NISHIMURA ◽  
Michiyasu SUZUKI ◽  
Kazuo MIZOI ◽  
Takashi YOSHIMOTO

2000 ◽  
Vol 143 (1) ◽  
pp. 207-209 ◽  
Author(s):  
L. Gürses ◽  
D. Yücelten ◽  
A. Cömert ◽  
T. Ergun ◽  
O. Gürbüz

PEDIATRICS ◽  
1975 ◽  
Vol 56 (6) ◽  
pp. 1078-1079
Author(s):  
Abdul J. Khan ◽  
Hugh E. Evans ◽  
Marylu R. Macabuhay ◽  
Yu-En Lee ◽  
Robert Werner

Beta-hemolytic Streptococcus group G, a rare human pathogen, has long been implicated in human disease as causing pharyngitis, puerperal sepsis, empyema, and even septicemia. We are reporting a rare, life-threatening, acute illness, primary peritonitis, due to this organism, whose etiological source probably was a family dog. Case Report R.K., a 2-year-old girl, was admitted with the complaints of anorexia, vomiting of three days' duration, and severe abdominal distension of one day's duration. The symptoms started following a burn injury over the face and lips three days prior to admission. Past history was noncontributory. Physical examination revealed an ill child of average size, fully conscious.


2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841


JPRAS Open ◽  
2019 ◽  
Vol 19 ◽  
pp. 67-72 ◽  
Author(s):  
Stephen R Ali ◽  
Susan A Hendrickson ◽  
Graham Collin ◽  
Jon Oxley ◽  
Robert P Warr

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