MOIN M, FARHOUDI A, MOIN A. PAPILLON-LEFE'VRE SYNDROME: NEUTROPHIL MOTILITY AND KILLING DEFECT IN A CHILD WITH RECURRENT SEVERE INFECTIONS. Med J Islam Repub Iran 1997; 11 (2) :149-152
URL:
http://mjiri.iums.ac.ir/article-1-1122-en.html
From the Department of Clinical Immunology and Allergy, Children's Medical Center, Tehran University of Medical Sciences, Tehran
Abstract: (4476 Views)
A case of palmoplantar hyperkeratosis with periodontosis and a history of
recurrent severe pyoderma, pneumonia and multiple liver abscesses is described
in a 12 year old girl. The patient demonstrated neutrophil dysfunction characterized
by decreased random migration and chemotaxis and defective bactericidal activity.
The exact immunopathological mechanism for susceptibility to infections in
Papillon-Lefe'vre syndrome patients still remains to be determined. However, the
mode of clinical presentation, laboratory findings and response to retinoid treatment,
all support the speculation of Papillon-Lefe'vre syndrome as a primary immunologic
disease with a variable defect in neutrophil motility and bactericidal activity. The
pattern of clinical presentations as skin and periodontal lesions alone or with
susceptibility to infection in other sites will change accordingly.
Type of Study:
case report |
Subject:
Immunology