IgG4-related skin disease, the Glossary
IgG4-related skin disease is the recommended name for skin manifestations in IgG4-related disease (IgG4-RD).[1]
Table of Contents
16 relations: Angiolymphoid hyperplasia with eosinophilia, Arthritis & Rheumatology, British Journal of Dermatology, Dermatology, Dermatology (journal), Eosinophilic cellulitis, Erythema, Gangrene, Histology, IgG4-related disease, Maculopapular rash, Pseudolymphoma, Psoriasis, Purpura, Raynaud syndrome, Urticarial vasculitis.
- IgG4-related disease
Angiolymphoid hyperplasia with eosinophilia
Angiolymphoid hyperplasia with eosinophilia (also known as: "Epithelioid hemangioma," "Histiocytoid hemangioma," "Inflammatory angiomatous nodule," "Intravenous atypical vascular proliferation," "Papular angioplasia," "Inflammatory arteriovenous hemangioma," and "Pseudopyogenic granuloma") usually presents with pink to red-brown, dome-shaped, dermal papules or nodules of the head or neck, especially about the ears and on the scalp. IgG4-related skin disease and Angiolymphoid hyperplasia with eosinophilia are IgG4-related disease.
See IgG4-related skin disease and Angiolymphoid hyperplasia with eosinophilia
Arthritis & Rheumatology
Arthritis & Rheumatology is a monthly peer-reviewed medical journal covering the natural history, pathophysiology, treatment, and outcome of the rheumatic diseases.
See IgG4-related skin disease and Arthritis & Rheumatology
British Journal of Dermatology
The British Journal of Dermatology is a monthly peer-reviewed medical journal that covers the field of dermatology.
See IgG4-related skin disease and British Journal of Dermatology
Dermatology
Dermatology is the branch of medicine dealing with the skin.
See IgG4-related skin disease and Dermatology
Dermatology (journal)
Dermatology is a peer-reviewed medical journal published by Karger Publishers.
See IgG4-related skin disease and Dermatology (journal)
Eosinophilic cellulitis
Eosinophilic cellulitis, also known as Wells' syndrome (not to be confused with Weil's disease), is a skin disease that presents with painful, red, raised, and warm patches of skin.
See IgG4-related skin disease and Eosinophilic cellulitis
Erythema
Erythema is redness of the skin or mucous membranes, caused by hyperemia (increased blood flow) in superficial capillaries.
See IgG4-related skin disease and Erythema
Gangrene
Gangrene is a type of tissue death caused by a lack of blood supply.
See IgG4-related skin disease and Gangrene
Histology
Histology, also known as microscopic anatomy or microanatomy, is the branch of biology that studies the microscopic anatomy of biological tissues.
See IgG4-related skin disease and Histology
IgG4-related disease (IgG4-RD), formerly known as IgG4-related systemic disease, is a chronic inflammatory condition characterized by tissue infiltration with lymphocytes and IgG4-secreting plasma cells, various degrees of fibrosis (scarring) and a usually prompt response to oral steroids.
See IgG4-related skin disease and IgG4-related disease
Maculopapular rash
A maculopapular rash is a type of rash characterized by a flat, red area on the skin that is covered with small confluent bumps.
See IgG4-related skin disease and Maculopapular rash
Pseudolymphoma
Pseudolymphoma is a benign lymphocytic infiltrate that resembles cutaneous lymphoma histologically, clinically, or both.
See IgG4-related skin disease and Pseudolymphoma
Psoriasis
Psoriasis is a long-lasting, noncontagious autoimmune disease characterized by patches of abnormal skin.
See IgG4-related skin disease and Psoriasis
Purpura
Purpura is a condition of red or purple discolored spots on the skin that do not blanch on applying pressure.
See IgG4-related skin disease and Purpura
Raynaud syndrome
Raynaud syndrome, also known as Raynaud's phenomenon, is a medical condition in which the spasm of small arteries causes episodes of reduced blood flow to end arterioles.
See IgG4-related skin disease and Raynaud syndrome
Urticarial vasculitis
Urticarial vasculitis (also known as "chronic urticaria as a manifestation of venulitis", "hypocomplementemic urticarial vasculitis syndrome", "hypocomplementemic vasculitis" and "unusual lupus-like syndrome") is a skin condition characterized by fixed urticarial lesions that appear histologically as a vasculitis.
See IgG4-related skin disease and Urticarial vasculitis
See also
- Angiolymphoid hyperplasia with eosinophilia
- Aortic aneurysm
- Aortic dissection
- Aortitis
- Autoimmune hypophysitis
- Autoimmune pancreatitis
- Benign lymphoepithelial lesion
- Cholecystitis
- Chronic sclerosing sialadenitis
- Idiopathic orbital inflammatory disease
- Idiopathic sclerosing mesenteritis
- IgG4-related disease
- IgG4-related ophthalmic disease
- IgG4-related prostatitis
- IgG4-related skin disease
- Inflammatory myofibroblastic tumour
- Interstitial nephritis
- Ligneous conjunctivitis
- Mastitis
- Mediastinitis
- Multifocal fibrosclerosis
- Parotitis
- Plasma cell granuloma
- Retroperitoneal fibrosis
- Riedel's thyroiditis