Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Language
Year range
1.
Revue Maghrebine de Pediatrie [La]. 2010; 20 (1): 49-54
in French | IMEMR | ID: emr-133606

ABSTRACT

The Kippel Trenaunay Weber syndrome is a rare entity. It is characterized by osteohypertrophic angiodysplasia. The vascular abnormalities touch especially the lymphatic and venous systems. However the existence of superficial or deep arteriovenous fistula is not rare. The deep one can have multiple visceral seats and put a strain on vital prognosis of patients in the event of a rupture. The authors report the case of a 9 year-old girl who presented a Klippel Trenaunay Weber Syndrome diagnosed on the occasion of a recurrent rectorrhagia which lead to severe anemia with 4,4g/100 ml of haemoglobin. The osteohypertrophic angiodysplasia touch the two inferior limbs. It is more marqued on the right side and extends to the lumbus. The colonoscopy found a rectosigmoidal fistula associated with a rectal prlapsus. The abdominal angioscan found multiple parietointestinal calcifications. It shows that vascular abnormalities in digestif tractus are diffuse. In the light of this case and the review of literature, the authors remind the clinical, para clinical aspects and difficulties of treatment of this rare entity

2.
Maroc Medical. 2002; 24 (3): 193-201
in French | IMEMR | ID: emr-60032

ABSTRACT

Behcet's disease is a predominantly venous vasculitis. It was first described as a clinical triad associating oral aphthae, genital aphthae and anterior uveitis. It concerns mainly young subjects of male gender originating from the Far-East and the Mediterranean basin. Its pathogenesis is not well known. It comprises neutrophil hyperreactivity owing to genetic predisposition, abnormalities in gd T cell function and microbial agents that could act as triggering factors. The most frequent clinical manifestations are cutaneo-mucous, ocular, vascular, neurological and articular. There is no specific biological abnormality and diagnosis is actually still purely based on clinical evidence. Treatment is not codified and only suspensive. It is based on colchicine, anti-inflammatory drugs and different immuno-supressives. In this work, we present a review on this subject according to some recent bibliographic data


Subject(s)
Humans , Vasculitis/etiology , Uveitis/etiology , Stomatitis, Aphthous
SELECTION OF CITATIONS
SEARCH DETAIL