IgG4-Related Skin Disease Presenting as a Pseudolymphoma in a White Adolescent Girl.


Journal

The American Journal of dermatopathology
ISSN: 1533-0311
Titre abrégé: Am J Dermatopathol
Pays: United States
ID NLM: 7911005

Informations de publication

Date de publication:
Sep 2019
Historique:
pubmed: 7 3 2019
medline: 6 2 2020
entrez: 7 3 2019
Statut: ppublish

Résumé

Immunoglobulin gamma (Ig) type 4-related disease (IgG4-RD) is a chronic immunologic systemic disorder that has gained worldwide recognition in the past decade. This entity can affect almost every organ system, and its characteristic lesions have been found in a variety of organs such as lacrimal and salivary glands, pancreas, liver, bile ducts, lungs, kidneys, retroperitoneum, breast, aorta, thyroid, and prostate. This case reports a very rare case of IgG4-RD presenting with a cutaneous lesion in a young female patient mimicking a lymphoproliferative disorder. IgG4-RD affecting the skin is a rare entity and has mostly been reported in Japanese men of middle to older age. IgG4-RD with cutaneous involvement should be in the differential of non-neoplastic, lymphomas, autoimmune, and infectious disorders of the skin.

Identifiants

pubmed: 30839348
doi: 10.1097/DAD.0000000000001401
doi:

Types de publication

Case Reports Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

675-679

Auteurs

Aria Shakeri (A)

University of Virginia School of Medicine, Charlottesville, VA.

Kimball Jade Kindley (KJ)

Department of Dermatology, University of Virginia School of Medicine, Charlottesville, VA.

Mary Margaret Noland (MM)

Department of Dermatology, University of Virginia School of Medicine, Charlottesville, VA.

Alejandro Ariel Gru (AA)

Department of Pathology, University of Virginia School of Medicine, Charlottesville, VA.

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Classifications MeSH