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获得性皮肤松弛症与多发性骨髓瘤相关:一例病例报告及文献复习

Cutis laxa acquisita associated with multiple myeloma: a case report and review of the literature.

作者信息

McCarty M J, Davidson J M, Cardone J S, Anderson L L

机构信息

Hematology/Oncology Service, Womack Army Medical Center, Fort Bragg, North Carolina, USA.

出版信息

Cutis. 1996 Apr;57(4):267-70.

PMID:8727781
Abstract

Cutis laxa acquisita is a rare disorder that affects collagen and elastin metabolism. The cause is unknown. Characteristic features include sagging and laxity of the skin, as well as involvement of the lungs, heart, gastrointestinal system, and urogenital tract. Three cases of cutis laxa acquisita have been reported in association with multiple myeloma. Due to the rarity of these disorders, a linkage has been postulated. The clinical and histologic data from the fourth case of cutis laxa acquisita associated with multiple myeloma were compared to the three other cases previously reported in the literature. The relationship between acquired cutis laxa and multiple myeloma is unclear, with only one case revealing possible immune-mediated elastin destruction via IgG immunoglobulin bound to dermal elastin fibers on immunofluoresence examination. No pattern in the clinical courses of the disorder can be seen on review of the four cases with coincident disease. We hypothesize that cutis laxa acquisita represents a paraneoplastic process of multiple myeloma, given the rarity of these diseases. Further investigation is necessary to determine the underlying linkage between these disorders. We suggest that serum and urine protein electrophoresis results be obtained in patients presenting with cutis laxa acquisita to screen for multiple myeloma given this association.

摘要

获得性皮肤松弛症是一种罕见的疾病,会影响胶原蛋白和弹性蛋白的代谢。病因不明。其特征性表现包括皮肤松弛下垂,以及肺部、心脏、胃肠道系统和泌尿生殖道受累。已有三例获得性皮肤松弛症与多发性骨髓瘤相关的报道。由于这些疾病罕见,有人推测它们之间存在联系。将第四例与多发性骨髓瘤相关的获得性皮肤松弛症的临床和组织学数据与文献中先前报道的其他三例进行了比较。获得性皮肤松弛症与多发性骨髓瘤之间的关系尚不清楚,只有一例在免疫荧光检查中显示通过与真皮弹性纤维结合的IgG免疫球蛋白可能存在免疫介导的弹性蛋白破坏。回顾这四例合并疾病的病例,未发现该疾病临床病程中的规律。鉴于这些疾病的罕见性,我们推测获得性皮肤松弛症代表多发性骨髓瘤的一种副肿瘤性过程。有必要进一步研究以确定这些疾病之间的潜在联系。鉴于这种关联,我们建议对患有获得性皮肤松弛症的患者进行血清和尿蛋白电泳检测,以筛查多发性骨髓瘤。

相似文献

1
Cutis laxa acquisita associated with multiple myeloma: a case report and review of the literature.获得性皮肤松弛症与多发性骨髓瘤相关:一例病例报告及文献复习
Cutis. 1996 Apr;57(4):267-70.
2
Multiple myeloma associated with acquired cutis laxa.与获得性皮肤松弛症相关的多发性骨髓瘤。
Cutis. 1980 Aug;26(2):209-11.
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Marked bilateral lower eyelid ectropion in cutis laxa: a paraneoplastic process in multiple myeloma.
Orbit. 2012 Jun;31(3):174-6. doi: 10.3109/01676830.2011.648808.
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Acquired cutis laxa associated with multiple myeloma.获得性皮肤松弛症伴多发性骨髓瘤。
Cutis. 2002 Feb;69(2):114-8.
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Acquired cutis laxa in a 55-year-old female with multiple myeloma and serologic evidence of systemic lupus erythematosus.一名55岁患有多发性骨髓瘤且有系统性红斑狼疮血清学证据的女性出现获得性皮肤松弛症。
Dermatol Online J. 2011 Jul 15;17(7):8.
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[Acquired cutis laxa and myeloma: large vacuolated cells in the dermis].[获得性皮肤松弛症与骨髓瘤:真皮中的大空泡细胞]
Ann Dermatol Venereol. 2007 Jun-Jul;134(6-7):548-51. doi: 10.1016/s0151-9638(07)89266-0.
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Acquired cutis laxa associated with multiple myeloma.获得性皮肤松弛症与多发性骨髓瘤相关。
Arch Dermatol. 1976 Jun;112(6):853-5.
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Acquired cutis laxa following urticarial vasculitis associated with IgA myeloma.与IgA骨髓瘤相关的荨麻疹性血管炎后获得性皮肤松弛症。
J Am Acad Dermatol. 2009 Jun;60(6):1052-7. doi: 10.1016/j.jaad.2008.09.059.
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Elastin production and degradation in cutis laxa acquisita.获得性皮肤松弛症中的弹性蛋白生成与降解
J Invest Dermatol. 1994 Oct;103(4):583-8. doi: 10.1111/1523-1747.ep12396893.
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Cutis Laxa Acquisita After Urticarial Vasculitis in SLE Patients.系统性红斑狼疮患者荨麻疹性血管炎后获得性皮肤松弛症
Am J Dermatopathol. 2018 Jun;40(6):433-437. doi: 10.1097/DAD.0000000000001084.

引用本文的文献

1
Primary systemic amyloidosis, acquired cutis laxa and cutaneous mucinosis in a patient with multiple myeloma.一名多发性骨髓瘤患者出现原发性系统性淀粉样变性、获得性皮肤松弛症和皮肤黏液瘤病。
An Bras Dermatol. 2013 Nov-Dec;88(6 Suppl 1):32-5. doi: 10.1590/abd1806-4841.20132531.
2
The complexity of elastic fibre biogenesis in the skin--a perspective to the clinical heterogeneity of cutis laxa.皮肤弹性纤维发生的复杂性——皮肤松弛症临床异质性的一个视角。
Exp Dermatol. 2013 Feb;22(2):88-92. doi: 10.1111/exd.12025. Epub 2012 Oct 23.