Polyneuropathy organomegaly endocrinopathy M-protein and skin changes syndrome with ascites as an early-stage manifestation: A case report

Polyneuropathy organomegaly endocrinopathy M-protein and skin changes (POEMS) syndrome is a rare paraneoplastic syndrome caused by a potential plasma cell tumor. The clinical manifestations of POEMS syndrome are diverse. Due to the insidious onset and lack of specific early-stage manifestations, POE...

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Published inWorld journal of clinical cases Vol. 11; no. 1; pp. 135 - 142
Main Authors Zhou, Xiao-Lei, Chang, Ying-Hao, Li, Lan, Ren, Juan, Wu, Xiao-Ling, Zhang, Xue, Wu, Peng, Tang, Shan-Hong
Format Journal Article
LanguageEnglish
Published United States Baishideng Publishing Group Inc 06.01.2023
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Summary:Polyneuropathy organomegaly endocrinopathy M-protein and skin changes (POEMS) syndrome is a rare paraneoplastic syndrome caused by a potential plasma cell tumor. The clinical manifestations of POEMS syndrome are diverse. Due to the insidious onset and lack of specific early-stage manifestations, POEMS syndrome is easily misdiagnosed or never diagnosed, leading to delayed treatment. Neurological symptoms are usually the first clinical manifestation, while ascites is a rare symptom in patients with POEMS syndrome. A female patient presented with unexplained ascites as an initial symptom, which is a rare early-stage manifestation of the condition. After 1 year, the patient gradually developed progressive renal impairment, anemia, polyserosal effusion, edema, swollen lymph nodes on the neck, armpits, and groin, and decreased muscle strength of the lower extremities. The patient was eventually diagnosed with POEMS syndrome after multidisciplinary team discussion. Treatment comprised bortezomib + dexamethasone, continuous renal replacement therapy, chest and abdominal closed drainage, transfusions of erythrocytes and platelets, and other symptomatic and supportive treatments. The patient's condition initially improved after treatment. However, then her symptoms worsened, and she succumbed to the illness and died. Ascites is a potential early manifestation of POEMS syndrome, and this diagnosis should be considered for patients with unexplained ascites. Furthermore, multidisciplinary team discussion is helpful in diagnosing POEMS syndrome.
Bibliography:Author contributions: Zhou XL and Chang YH were the patient’s physicians, reviewed the literature, and contributed to manuscript drafting; Li L, Ren J, and Wu XL contributed to manuscript drafting and interpreted the imaging findings; Zhang X and Wu P contributed to revision of the manuscript; Tang SH was responsible for revising the manuscript for important intellectual content; All authors approved the final submitted version of the manuscript.
Corresponding author: Shan-Hong Tang, MD, PhD, Assistant Professor, Associate Chief Physician, Director, Graduate School, Southwest Medical University, No. 319 Section 3 Zhongshan Road, Luzhou 646099, Sichuan Province, China. shanhongtang@163.com
ISSN:2307-8960
2307-8960
DOI:10.12998/wjcc.v11.i1.135