Upper Digestive Hemorrhage as Clinical Presentation of Leukocytoclastic Vasculitis: An Unusual Endoscopic Diagnosis

Endoscopy ◽  
1993 ◽  
Vol 25 (08) ◽  
pp. 542-543 ◽  
Author(s):  
C. Martin de Argila ◽  
A. L. Sanroman ◽  
V. F. Moreira ◽  
M. Garcia Gonzalez ◽  
I. Alvarez Baleriola
1993 ◽  
Vol 17 (4) ◽  
pp. 349
Author(s):  
Eduardo M. Targarona ◽  
Inmaculada Pros ◽  
Carmen Balagué ◽  
Carlos Parada ◽  
Jaume Ordi ◽  
...  

Chirurgia ◽  
2016 ◽  
Vol 111 (6) ◽  
pp. 505 ◽  
Author(s):  
Claudiu Turculet ◽  
Dragos Ene ◽  
Teodor Florin Georgescu ◽  
E. Ciuca ◽  
A. Vladascau ◽  
...  

1982 ◽  
Vol 83 (2) ◽  
pp. 410-416 ◽  
Author(s):  
P. Rutgeerts ◽  
G. Vantrappen ◽  
L. Broeckaert ◽  
J. Janssens ◽  
G. Coremans ◽  
...  

2019 ◽  
Vol 6 (2) ◽  
pp. 537
Author(s):  
Mohammed S. Alharbi

Acute hemorrhagic edema of infancy (AHEI) is an unusual form of leukocytoclastic vasculitis with dramatic distinguishing skin lesions that occurs in infants who age 4 to 24 months old. Clinical presentation at onset requires clinical and, less often, histological evaluation to distinguish it from more serious diseases and other vasculitis. Treatment of AHEI remains controversial; and since it is a self-limiting disease, a conservative approach should be considered first. Although some authors have reported that the use of steroids may be beneficial if started early on, we think their use, based on our presented cases here, may accelerate the healing and improves the color of preexisting skin lesions but does not significantly alter the course of the disease. Authors reported here two clinical Cases of AHEI (Diagnosed based on characteristic skin lesions and confirmed with Histological evaluation) who were treated initially with systemic steroids, besides we reviewed the role of systemic steroids in the treatment of AHEI.


Author(s):  
Amal Hajri ◽  
Oussama Lafkih ◽  
Driss Erguibi ◽  
Saad Rifki El Jai ◽  
Rachid Boufettal ◽  
...  

Liver abscesses secondary to bilio-enteric fistulas are rare and therefore unknown to the attending physician. In this report, we present a bilio-enteric communication, between the gallbladder; which was macro lithiasic; and the stomach revealed by an upper digestive hemorrhage in a septic context in a 34 year old man. A pyogenic bacterial liver abscess developed because of the fistula without biliary obstruction. The patient was treated surgically with disconnection of the fistula and drainage of the abscess. The liver abscess is probably due to the contamination of the bile by the cholecysto-gastric fistula. The germ isolated was a citrobacter freundii which is rarely involved in liver abscesses.


2020 ◽  
Vol 8 (7) ◽  
pp. 741-743
Author(s):  
El Oukli Yassir ◽  
Youssef Kerroum ◽  
Mohamed Alaoui Maliki ◽  
Khedid Yahya Zin El Abidin ◽  
Mohamed El Absi ◽  
...  

2021 ◽  
pp. 1-5
Author(s):  
Oghowan Abdelrahman ◽  
Andleeb Shadan ◽  
Laila Al Dabal ◽  
Tasnim R. Keloth

On 11 March 2020, WHO declared the SARS-CoV-2 outbreak as a pandemic, representing a public health emergency of unprecedented dimension. COVID-19 is a multisystem Novel viral infection with protean manifestations and variable degrees of clinical presentation. The most common presentation is upper and lower respiratory tract illness. Cutaneous manifestations of COVID-19 have rarely been described. In this case report, we present a 41-year-old male patient who presented with fatigue and follicular skin rash followed almost 2 weeks later with fever, left upper limb transient weakness, and pneumonia. Of interest is that the patient’s skin lesions tested positive on COVID-19 antigen test. The patient received a course of anti-COVID-19 treatment as per our national guideline, and he made a full clinical and radiology recovery.


Author(s):  
Line Buhl ◽  
David Muirhead

There are four lysosomal diseases of which the neuronal ceroid lipofuscinosis is the rarest. The clinical presentation and their characteric abnormal ultrastructure subdivide them into four types. These are known as the Infantile form (Santavuori-Haltia), Late infantile form (Jansky-Bielschowsky), Juvenile form (Batten-Spielmeyer-Voght) and the Adult form (Kuph's).An 8 year old Omani girl presented wth myclonic jerks since the age of 4 years, with progressive encephalopathy, mental retardation, ataxia and loss of vision. An ophthalmoscopy was performed followed by rectal suction biopsies (fig. 1). A previous sibling had died of an undiagnosed neurological disorder with a similar clinical picture.


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