A disease difficult to diagnose: Gardner-Diamond syndrome accompanied by platelet dysfunction.

Abstract

Gardner Diamond syndrome is a rare condition characterized with painful ecchymoses in different parts of the body and cutaneous and mucosal hemorrhages. The etiology is not known fully and psychogenic factors are thought to be involved. Cutaneous lesions and hemorrhages develop mostly following emotional stress and rarely minor traumas and may recur. Although the extremities are involved with the highest rate, the lesions may be observed in any part of the body. Hemostatic tests are generally normal. The majority of the subjects is composed of young women. It is observed more rarely in men and children. In this article, a patient who presented with recurring painful echymoses and bleeding disorder and diagnosed with Gardner Diamond syndrome by intracutaneous injection of autologous blood was presented to emphasize that this syndrome is observed rarely in the childhood and should be considered not only in the differential diagnosis of cutaneous lesions, but also in the differential diagnosis of various system hemorrhages.

• Authors: Zeynep Karakaş, Serap Karaman, Burcu Avcı, Ayşegül Ünüvar, Gülyüz Öztürk, Sema Anak, Ömer Devecioğlu
• Journal: Turk pediatri arsivi (Turk Pediatri Ars) Vol. 49 Issue 3 Pg. 250-3 (Sep 2014) ISSN: 1306-0015 [Print] Turkey
• PMID: 26078671 (Publication Type: Case Reports)