Torres-Saavedra Fabio, León-Sierra Lina
Division of Rheumatology, GRUA Investigation Group, Universidad de Antioquia, 050010, Medellín, Colombia.
IPS Artmedica, Medellín, Colombia.
BMC Rheumatol. 2022 May 19;6(1):26. doi: 10.1186/s41927-022-00258-y.
POEMS syndrome is a rare paraneoplastic syndrome caused by plasma cell disorder almost always lambda restricted. Secondary Raynaud's phenomenon is an overlooked skin manifestation of the disease even though it is present in twenty percent of patients. On POEMS syndrome have not been described positive antinuclear antibodies (ANA) and this could lead to a misdiagnosis of autoimmune disease, mainly systemic sclerosis.
A 47-year-old man presented with color changes on fingertips consistent with biphasic Raynaud's phenomenon; an antinuclear antibody test was positive (at 1:320 titers in a speckled pattern) with normal nailfold capillaroscopy. Clinical features of systemic sclerosis were absent. Twenty-four months later, the patient presented symmetric sensorimotor demyelinating polyneuropathy, and he was diagnosed with Guillain-Barre syndrome; treatment with intravenous gammaglobulin had an incomplete response. Raynaud's phenomenon persisted associated with acrocyanosis, white nails, and positive ANA (1:1280 in a nucleolar pattern). POEMS syndrome was suspected, and serum protein electrophoresis (SPEP) was done. The SPEP revealed polyclonal gammopathy, and serum immunofixation showed monoclonal (M)-protein (IgG lambda). Serum vascular endothelial growth factor concentration showed increased levels. The patient was diagnosed with POEMS syndrome, and treatment with lenalidomide and dexamethasone improved the Raynaud's phenomenon, acrocyanosis, and white nails, but the neurological response was partial.
POEMS syndrome may mimic clinical manifestations of systemic sclerosis v.g. Raynaud's phenomenon, skin thickening, telangiectasia, and positive ANA. Raynaud's phenomenon may precede other clinical manifestations of POEMS syndrome by several months. It is necessary to have a high index of suspicion for the diagnosis, especially in patients with peripheral polyneuropathy and monoclonal paraprotein. The significance of positive ANA in this condition is unknown and deserves further investigation.
POEMS综合征是一种罕见的副肿瘤综合征,由浆细胞疾病引起,几乎总是λ限制型。继发性雷诺现象是该疾病一种被忽视的皮肤表现,尽管20%的患者存在此现象。POEMS综合征患者中尚未有抗核抗体(ANA)阳性的报道,这可能导致误诊为自身免疫性疾病,主要是系统性硬化症。
一名47岁男性出现指尖颜色变化,符合双相雷诺现象;抗核抗体检测呈阳性(斑点型,滴度为1:320),甲襞毛细血管镜检查正常。无系统性硬化症的临床特征。24个月后,患者出现对称性感觉运动性脱髓鞘性多发性神经病,被诊断为吉兰 - 巴雷综合征;静脉注射免疫球蛋白治疗反应不完全。雷诺现象持续存在,并伴有手足发绀、白甲和ANA阳性(核仁型,1:1280)。怀疑为POEMS综合征,进行了血清蛋白电泳(SPEP)检查。SPEP显示多克隆丙种球蛋白病,血清免疫固定显示单克隆(M)蛋白(IgG λ)。血清血管内皮生长因子浓度升高。患者被诊断为POEMS综合征,来那度胺和地塞米松治疗改善了雷诺现象、手足发绀和白甲,但神经反应部分改善。
POEMS综合征可能模仿系统性硬化症的临床表现,如雷诺现象、皮肤增厚、毛细血管扩张和ANA阳性。雷诺现象可能比POEMS综合征的其他临床表现早出现数月。诊断时必须高度怀疑,特别是对于患有周围性多发性神经病和单克隆副蛋白的患者。这种情况下ANA阳性的意义尚不清楚,值得进一步研究。