Background: Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by progressive cerebellar ataxia, growth retardation, immunodeficiency, chronic pulmonary disease and chromosomal instability. Cutaneous granulomas are a known phenomenon in A-T but extra-dermal manifestation of granulomas at bone and synovia has not been reported so far. The clinical presentation, immunological findings, the long-term course and treatment options of eight patients with severe granulomas will be reported.Methods: From our cohort of 44 classical A-T patients, eight patients aged 2–11 years (18.2%) presented with granulomas. Immunological features of patients with and without granulomas were compared. Five patients suffered from cutan...
We report the case of a 55-year-old Japanese patient with granuloma faciale (GF) successfully treate...
A 36-year-old male with anaplastic large T cell lymphoma (A; nodal manifestations in the left iliac ...
Ataxia-Telangiectasia is a rare multisystem autosomal recessive disorder [OMIM 208900], caused by mu...
Background: Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by prog...
Background: Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by prog...
Background: Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by prog...
Background: Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by prog...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
textabstractBackground: Non-infective cutaneous granulomas with unknown pathogenesis occur in variou...
Ataxia-telangiectasia (A-T) is a complex multisystem disorder characterized by progressive neurologi...
Development of cutaneous granulomas in 8 patients with ataxia-telangiectasia is reported from the De...
with an appropriate T-cell receptor reper-toire and the unopposed activity of T cells and/or nat...
Ataxia-telangiectasia (A-T) is a complex multisystem disorder characterized by progressive neurologi...
Granulomatosis with polyangiitis (GPA) is a granulomatous disorder linked with systemic necrotizing ...
Background: Granuloma annulare (GA) is a benign, usually self-limited, inflammatory skin disease. Al...
We report the case of a 55-year-old Japanese patient with granuloma faciale (GF) successfully treate...
A 36-year-old male with anaplastic large T cell lymphoma (A; nodal manifestations in the left iliac ...
Ataxia-Telangiectasia is a rare multisystem autosomal recessive disorder [OMIM 208900], caused by mu...
Background: Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by prog...
Background: Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by prog...
Background: Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by prog...
Background: Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by prog...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
textabstractBackground: Non-infective cutaneous granulomas with unknown pathogenesis occur in variou...
Ataxia-telangiectasia (A-T) is a complex multisystem disorder characterized by progressive neurologi...
Development of cutaneous granulomas in 8 patients with ataxia-telangiectasia is reported from the De...
with an appropriate T-cell receptor reper-toire and the unopposed activity of T cells and/or nat...
Ataxia-telangiectasia (A-T) is a complex multisystem disorder characterized by progressive neurologi...
Granulomatosis with polyangiitis (GPA) is a granulomatous disorder linked with systemic necrotizing ...
Background: Granuloma annulare (GA) is a benign, usually self-limited, inflammatory skin disease. Al...
We report the case of a 55-year-old Japanese patient with granuloma faciale (GF) successfully treate...
A 36-year-old male with anaplastic large T cell lymphoma (A; nodal manifestations in the left iliac ...
Ataxia-Telangiectasia is a rare multisystem autosomal recessive disorder [OMIM 208900], caused by mu...