Common variable immunodeficiency and eosinophilic fasciitis

European Journal of Dermatology

Volumn 12, Issue 1, 2002, Pages 73-74

  Di Gioacchino, Mario ^a   Masci, Silvio ^a   Paolini, Franco ^a   Verna, Nicola ^a   Angelucci, Domenico ^a   Cavallucci, Enrico ^a   Paganelli, Roberto ^a  

^a Section of Allergy   (Italy)

Author keywords

Common variable immunodeficiency; Eosinophilic fasciitis; Hypogammaglobulinemia

Indexed keywords

IMMUNOGLOBULIN CLASS;

ADULT; ARTICLE; CASE REPORT; COMMON VARIABLE IMMUNODEFICIENCY; DISEASE ASSOCIATION; EOSINOPHILIC FASCIITIS; FEMALE; HUMAN; HYPOGAMMAGLOBULINEMIA; IMMUNOSUPPRESSIVE TREATMENT; PROTEIN DEPLETION; SKIN BIOPSY;

AGAMMAGLOBULINEMIA; ANKLE JOINT; ARM; BIOPSY; COMMON VARIABLE IMMUNODEFICIENCY; EOSINOPHILIA; FASCIITIS; FEMALE; HUMANS; IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; LEG; MIDDLE AGED;

EID: 0036162002     PISSN: 11671122     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Diffuse fasciitis with hypergammaglobulinaemia and eosinophilia, a new syndrome?
2. Eosinophilic fasciitis in children
3. Localized forms of scleroderma, including morphea, linear scleroderma, and eosinophilic fasciitis
4. Eosinophilic fasciitis - A case with hypogammaglobuinaemia
5. Common variable immunodeficiency: Clinical and immunological features of 248 patients
6. B cell lines from a subset of patient with common variable immunodeficiency undergo enhanced apoptosis associated with an increased display of CD95 (Apo-1/fas) diminished CD38 expression, and decreased IgG and IgA production