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Autoerythrocyte sensitization syndrome: Gardner-Diamond syndrome

机译:自身红细胞致敏综合征:Gardner-Diamond综合征

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Autoerythrocyte sensitization syndrome is a disease that mostly affects young woman and characterized by painful localized inflamation and ecchymoses. Ecchymoses can occur spontaneously, particularly with emotional stress and after mild trauma. The syndrome was described by Gardner and Diamond who concluded that the accompanying ecchymoses was the result of autosensitization to extravasated erythrocytes after tissue trauma. To support this conclusion they reproduced similar lesions by intradermal injections of autologous erythrocyte suspensions. The extremities are most commonly involved and an association with somatic and psychiatric syndromes has been recognised. AES syndrome should be considered in the differential diagnosis of factitial purpura and coagulopathies. A case of 21 year-old-female who has signs of emotional and somatic disturbance including depression, anxiety, headaches, insomnia, anorexia, muscle and joint aches with several episodes of circular ecchymoses on her arms and legs is presented and the literature is reviewed. The diagnosis was confirmed by induction of similar lesions by intradermal injection of the patient’s own erythrocytes.
机译:自身红细胞致敏综合症是一种主要影响年轻女性的疾病,其特征是局部发炎和瘀斑疼痛。瘀斑可自发发生,尤其是在情绪紧张和轻度创伤后。该综合征由Gardner和Diamond描述,他们得出结论,伴随的瘀斑是组织创伤后对渗出的红细胞自动敏化的结果。为了支持该结论,他们通过皮内注射自体红细胞悬液重现了相似的病变。肢体最常见,并且已经认识到与躯体和精神病综合症有关。在对事实性紫癜和凝血病的鉴别诊断中应考虑AES综合征。介绍了一个21岁女性的病例,该患者的情绪和躯体障碍包括抑郁症,焦虑症,头痛,失眠症,厌食症,肌肉和关节痛,胳膊和腿上有数次环状瘀斑发作,并对其文献进行了回顾。 。通过皮内注射患者自身的红血球诱导相似的病变,证实了诊断。

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