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利妥昔单抗治疗格雷夫斯病所致对皮质类固醇耐药的突眼、黏液性水肿和骨关节炎综合征的效用:一例报告

Utility of rituximab treatment for exophthalmos, myxedema, and osteoarthropathy syndrome resistant to corticosteroids due to Graves' disease: a case report.

作者信息

Ferreira-Hermosillo Aldo, Casados-V Ruben, Paúl-Gaytán Pedro, Mendoza-Zubieta Victoria

机构信息

Unidad de Investigación Médica en Endocrinología Experimental, Hospital de Especialidades, Centro Médico Nacional Siglo XXI, IMSS, Cuauhtémoc 330, colonia Doctores, Delegación Cuauhtémoc, Mexico City, CP 06720, Mexico.

Departamento de Endocrinología, Hospital de Especialidades, Centro Médico Nacional Siglo XXI, IMSS, Mexico City, Mexico.

出版信息

J Med Case Rep. 2018 Feb 16;12(1):38. doi: 10.1186/s13256-018-1571-9.

Abstract

BACKGROUND

Exophthalmos, myxedema, and osteoarthropathy syndrome is a very rare condition that is associated with Graves' disease. The presence of dermopathy and the involvement of joint/bone tissues indicate that it seems to be related with the severity of the autoimmune process. Owing to its low incidence, there is a lack of information regarding its treatment and clinical follow-up. Some cases improved after use of high doses of steroids; however, some patients do not respond to this treatment. Recently, the effectiveness of rituximab for treatment of Graves' ophthalmopathy resistant to corticosteroids has been demonstrated. However, it has never been used for the treatment of exophthalmos, myxedema, and osteoarthropathy syndrome (particularly for the treatment of osteoarticular manifestations).

CASE PRESENTATION

We present the case of a 54-year-old Mexican woman previously treated for Graves' disease who developed post-iodine hypothyroidism and exophthalmos, myxedema, and osteoarthropathy that did not improve after high doses of steroids (intravenous and oral). Her exophthalmos, myxedema, and osteoarthropathy syndrome symptoms improved as early as 6 months after treatment with rituximab.

CONCLUSION

Exophthalmos, myxedema, and osteoarthropathy syndrome is a non-classical presentation of Graves' disease, whose clinical manifestations could improve after treatment with rituximab, particularly in those patients with lack of response to high doses of corticosteroids.

摘要

背景

突眼、黏液性水肿和骨关节炎综合征是一种与格雷夫斯病相关的非常罕见的病症。皮肤病变的存在以及关节/骨组织的受累表明它似乎与自身免疫过程的严重程度有关。由于其发病率低,缺乏关于其治疗和临床随访的信息。一些病例在使用高剂量类固醇后有所改善;然而,一些患者对这种治疗没有反应。最近,已证明利妥昔单抗对治疗抵抗皮质类固醇的格雷夫斯眼病有效。然而,它从未用于治疗突眼、黏液性水肿和骨关节炎综合征(特别是用于治疗骨关节表现)。

病例报告

我们报告一例54岁墨西哥女性病例,该患者曾接受格雷夫斯病治疗,出现碘后甲状腺功能减退以及突眼、黏液性水肿和骨关节炎,高剂量类固醇(静脉和口服)治疗后未见改善。使用利妥昔单抗治疗后6个月,她的突眼、黏液性水肿和骨关节炎综合征症状就有所改善。

结论

突眼、黏液性水肿和骨关节炎综合征是格雷夫斯病的一种非典型表现,其临床表现用利妥昔单抗治疗后可能改善,特别是在那些对高剂量皮质类固醇无反应的患者中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5744/5815205/0490ba82e62a/13256_2018_1571_Fig1_HTML.jpg

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