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Review
. 2017 Sep;38(9):623-627.
doi: 10.1016/j.revmed.2017.01.008. Epub 2017 Mar 28.

[Gardner-Diamond syndrome in a young man: A case report and literature review]

[Article in French]
Affiliations
Review

[Gardner-Diamond syndrome in a young man: A case report and literature review]

[Article in French]
P Henneton et al. Rev Med Interne. 2017 Sep.

Abstract

Introduction: Gardner-Diamond syndrome is a rare condition secondary to a sensitization to self-erythrocytes. It is predominantly seen in women and presents as a painful ecchymotic disorder. An underlying psychiatric disease or a triggering psychological stress is of important diagnostic value.

Case report: We report a 24-year-old patient who presented with intermittent spontaneous painful ecchymosis since 5 years. Complementary investigations failed to identify an organic disorder. Gardner-Diamond syndrome was retained because of the clinical presentation, the negativity of diagnostic work-up and the identification of a psychological trauma. Patient management (pain, psychological support) is difficult, justifying a multidisciplinary approach.

Conclusion: Gardner-Diamond syndrome is a rare and unrecognized disorder, which should be discussed in the presence of ecchymotic or purpuric lesions that do not have a diagnostic orientation. Early recognition of this disorder enables initiation of an appropriate management, but also limits unnecessary additional explorations.

Keywords: Autoerythrocyte sensitization syndrome; Gardner–Diamond syndrome; Painful bruising syndrome; Psychogenic purpura; Purpura psychogénique; Syndrome de Gardner-Diamond; Syndrome des ecchymoses douloureuses; Syndrome d’autosensibilisation érythrocytaire.

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