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一名患有特发性骨髓纤维化和胸腺瘤-重症肌无力-免疫缺陷综合征患者患Sweet综合征:依曲替酯治疗的疗效

Sweet's syndrome in a patient with idiopathic myelofibrosis and thymoma-myasthenia gravis-immunodeficiency complex: efficacy of treatment with etretinate.

作者信息

Altomare G, Capella G L, Frigerio E

机构信息

Istituto di Dermatologia, Università degli Studi di Milano, Italy.

出版信息

Haematologica. 1996 Jan-Feb;81(1):54-8.

PMID:8900854
Abstract

Here we present the case of a patient affected with a unique association of Sweet's syndrome, idiopathic myelofibrosis, spindle-cell thymoma, myasthenia gravis and Good's syndrome (a rare form of thymoma-related, combined immunodeficiency presenting with recurrent respiratory infections). Conventional therapies (corticosteroids, colchicine, DDS, clofazimine) were ineffective or were contraindicated. Treatment with etretinate (50 mg/day) proved effective on skin lesions. Moreover, the patient's general condition unexpectedly improved, with long-lasting (11 months) suppression of respiratory infections and a slight but consistent improvement of hematological parameters such as Hct, MCV, Hb level, RBC, WBC and lymphocyte absolute counts.

摘要

在此,我们报告一例患者,其患有Sweet综合征、特发性骨髓纤维化、梭形细胞胸腺瘤、重症肌无力和Good综合征(一种罕见的与胸腺瘤相关的联合免疫缺陷,表现为反复呼吸道感染)的独特关联。传统疗法(皮质类固醇、秋水仙碱、氨苯砜、氯法齐明)无效或禁忌使用。依曲替酯(50毫克/天)治疗对皮肤病变有效。此外,患者的总体状况意外改善,呼吸道感染得到长期(11个月)抑制,血液学参数如红细胞压积、平均红细胞体积、血红蛋白水平、红细胞、白细胞和淋巴细胞绝对计数有轻微但持续的改善。

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