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[下肢淋巴水肿:脊柱关节病的一种罕见表现]

[Lower limb lymphedema: A rare manifestation of spondyloarthropathy].

作者信息

Fourgeaud C, Vignes S

机构信息

Unité de Lymphologie, site constitutif du Centre national de référence des maladies vasculaires rares (lymphœdèmes primaires), hôpital Cognacq-Jay, 15, rue Eugène-Millon, 75015 Paris, France.

Unité de Lymphologie, site constitutif du Centre national de référence des maladies vasculaires rares (lymphœdèmes primaires), hôpital Cognacq-Jay, 15, rue Eugène-Millon, 75015 Paris, France.

出版信息

Rev Med Interne. 2019 Dec;40(12):837-840. doi: 10.1016/j.revmed.2019.06.007. Epub 2019 Jul 3.

DOI:10.1016/j.revmed.2019.06.007
PMID:31279481
Abstract

INTRODUCTION

Spondyloarthritis include articular (axial, peripheral or enthesitic) and extra-articular manifestations. We reported three cases of limb lymphedema associated with a spondyloarthritis.

CASE REPORTS

We report on two men and one female aged of 75, 52 and 39 years, respectively. The rheumatic disease was an ankylosing spondylitis HLA B27 positive in two patients and a psoriatic arthritis in the remaining one. Lymphedema, always unilateral, confirmed by the Stemmer's sign, involved the whole lower limb (n=2) or only the foot and calf (n=1). Lymphedema occurred 3 months, 40 and 9 years after the onset of spondyloarthritis. Lower limb lymphoscintigraphy was abnormal in all cases: decrease (n=2) or absence (n=1) of inguinal lymph node uptake, and visualization of the popliteal lymph node related to deep lymphatic pathway (n=1). Treatment of the spondyloarthritis did not improve lymphedema. Both the low-stretch bandage and elastic compression treatment allowed its reduction and stabilization.

CONCLUSION

Limb lymphedema is a rare extra-articular manifestation of spondyloarthritis. Its course appears to be independent of joint disease. Its management is specific and should be associated to that of the rheumatologic disorder.

摘要

引言

脊柱关节炎包括关节(中轴、外周或附着点相关)和关节外表现。我们报告了3例与脊柱关节炎相关的肢体淋巴水肿病例。

病例报告

我们报告了2名男性和1名女性,年龄分别为75岁、52岁和39岁。其中2例风湿性疾病为HLA B27阳性的强直性脊柱炎,另1例为银屑病关节炎。淋巴水肿均为单侧,通过施特默征确诊,累及整个下肢(2例)或仅累及足和小腿(1例)。淋巴水肿发生在脊柱关节炎发病后3个月、40年和9年。所有病例下肢淋巴闪烁造影均异常:腹股沟淋巴结摄取减少(2例)或缺失(1例),腘窝淋巴结通过深部淋巴途径显影(1例)。脊柱关节炎的治疗并未改善淋巴水肿。低弹性绷带和弹力压迫治疗均能减轻并稳定病情。

结论

肢体淋巴水肿是脊柱关节炎一种罕见的关节外表现。其病程似乎与关节疾病无关。其治疗具有特殊性,应与风湿性疾病的治疗相结合。

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