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角层下脓疱性皮肤病与IgA骨髓瘤。

Subcorneal pustular dermatosis and IgA myeloma.

作者信息

Atukorala D N, Joshi R K, Abanmi A, Jeha M T

机构信息

Riyadh Armed Forces Hospital, Saudi Arabia.

出版信息

Dermatology. 1993;187(2):124-6. doi: 10.1159/000247221.

DOI:10.1159/000247221
PMID:8358100
Abstract

A case of subcorneal pustular dermatosis (SCPD), as a presenting feature in a patient with multiple myeloma, is described. This is the seventh case report of this association and the first from the Middle East. Five of these cases, including the present report, have been of the IgA paraprotein type, IgA intraepidermal deposits have been described in a few patients with SCPD associated with IgA paraproteinaemias but have not been detected in our patient.

摘要

本文描述了一例以角膜下脓疱性皮肤病(SCPD)为首发特征的多发性骨髓瘤患者。这是该关联的第七例病例报告,也是中东地区的首例报告。包括本报告在内的其中五例病例为IgA副蛋白类型,少数伴有IgA副蛋白血症的SCPD患者有IgA表皮内沉积的描述,但在我们的患者中未检测到。

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Subcorneal pustular dermatosis and IgA myeloma.角层下脓疱性皮肤病与IgA骨髓瘤。
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Immune-Mediated Dermatoses in Patients with Haematological Malignancies: A Comprehensive Review.血液系统恶性肿瘤患者的免疫介导性皮肤病:全面综述。
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Subcorneal pustular dermatosis in childhood: a case report and review of the literature.
儿童角层下脓疱性皮肤病:一例报告并文献复习
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IgA pemphigus associated with monoclonal gammopathy completely resolved after achievement of complete remission of multiple myeloma with bortezomib, cyclophosphamide and dexamethasone regimen.硼替佐米、环磷酰胺和地塞米松方案治疗多发性骨髓瘤达到完全缓解后,IgA 天疱疮伴单克隆丙种球蛋白病完全消退。
Wien Klin Wochenschr. 2010 May;122(9-10):311-4. doi: 10.1007/s00508-010-1361-x.