The characteristics of ascites in patients with POEMS syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00277-013-1829-7.pdf
Reference22 articles.
1. Nakanishi T, Sobue I, Toyokura Y, Nishitani H, Kuroiwa Y, Satoyoshi E et al (1984) The Crow–Fukase syndrome: a study of 102 cases in Japan. Neurology 34:712–720
2. Cui RT, Huang XS, Shi Q, Tian CL, Liu JX, Pu CQ (2011) POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes) syndrome in China. Intern Med J 41:481–485
3. Bardwick PA, Zveifler NJ, Gill GN, Newman D, Greenway GD, Resnick DL (1980) Plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, M protein and skin changes: the POEMS syndrome. Medicine 59:311–322
4. Dispenzieri A (2012) POEMS syndrome: update on diagnosis, risk-stratification, and management. Am J Hematol 87:804–814
5. Singh D, Wadhwa J, Kumar L, Raina V, Agarwal A, Kochupillai V (2003) POEMS syndrome: experience with fourteen cases. Leuk Lymphoma 44:1749–1752
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1. POEMS syndrome: Update on diagnosis, risk‐stratification, and management;American Journal of Hematology;2023-09-21
2. Porto-sinusoidal vascular disorder, report of a novel association with POEMS syndrome. Future challenge for the hepatologist;Clinics and Research in Hepatology and Gastroenterology;2023-05
3. Polyneuropathy organomegaly endocrinopathy M-protein and skin changes syndrome with ascites as an early-stage manifestation: A case report;World Journal of Clinical Cases;2023-01-06
4. From hepatomegaly to POEMS syndrome: A case report;Hepatology Forum;2023
5. A POEMS syndrome patient with idiopathic non-cirrhotic portal hypertension received the transjugular intrahepatic portosystemic shunt: a case report and literature review;Nigerian Journal of Clinical Practice;2022
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