منابع مشابه
Autoerythrocyte Sensitization or Psychogenic Purpura?
The above quotation is taken from the original clinical report in which Gardner and Diamond (1955) described the syndrome of autoerythrocyte sensitization as an unusual purpuric syndrome in which crops of apparently spontaneous painful inflammatory ecchymoses occurred in four women who had sustained physical injury shortly before the onset of symptoms. They postulated that, as a result, their p...
متن کاملPsychogenic Purpura Successfully Treated with Antidepressant Therapy
Psychogenic purpura (PP) or Gardner-Diamond syndrome is a very rare condition characterized by spontaneous, recurrent, and painful edematous skin lesions progressing to ecchymoses [1]. Bleeding from the nose, gastrointestinal organs, kidneys, and uterus has also been reported [2]. PP is commonly regarded as an autoimmune vasculopathy with sensitization to phosphatidylserine, a component of eryt...
متن کامل[Psychogenic purpura with hematuria and sexual pain disorder: a case report].
Psychogenic purpura (Gardner-Diamond syndrome) is the occurrence and spontaneous recurrence of painful ecchymosis following emotional stress and minor trauma. Although the exact mechanism of this syndrome remains unknown, apart from skin lesions, different types of hemorrhaging have been reported, such as epistaxis, gastrointestinal bleeding, and bleeding from the ear canals and eyes. We report...
متن کاملUnique endoscopic images in a patient with Henoch-Schönlein purpura.
A 59-year-old woman was admitted to the dermatology section for a skin eruption. She was initially diagnosed as having a drug-induced skin rash. Endoscopic examination performed for severe abdominal pain and melena revealed a reddish elevated lesion with an ulceration on the top in the descending part of her duodenum (Picture 1). While a duodenal tumor was suspected, a biopsy was not performed ...
متن کاملIdiopathic thrombocytopenic purpura: a practice guideline developed by explicit methods for the American Society of Hematology.
DIOPATHIC thrombocytopenic purpura (ITP, also I known as primary immune thrombocytopenic purpura) is a hematologic disorder for which appropriate diagnostic and treatment strategies are uncertain. In 1994, the American Society of Hematology (ASH) established a panel to produce explicitly developed practice guidelines for the diagnosis and management of ITP. “Explicitly developed,” evidencebased...
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ژورنال
عنوان ژورنال: American Journal of Hematology
سال: 1997
ISSN: 0361-8609,1096-8652
DOI: 10.1002/(sici)1096-8652(199707)55:3<146::aid-ajh5>3.0.co;2-s