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Thematische Bibliographien / POEMS syndrom / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „POEMS syndrom“

Autor: Grafiati

Veröffentlicht am 8. Februar 2025

Zuletzt aktualisiert am 31. Juli 2025

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1

Schwarz, Ricarda, and Marius Horger. "POEMS-Syndrom." RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren 190, no. 02 (2018): 106–10. http://dx.doi.org/10.1055/s-0043-121581.

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2

Braun, S. A., P. Albrecht, A. Methner, and S. Hanneken. "POEMS-Syndrom." Der Hautarzt 62, no. 10 (2011): 722–25. http://dx.doi.org/10.1007/s00105-011-2239-1.

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3

Cohnen, Mathias, Michael Uppenkamp, Peter Meusers, and Günter Brittinger. "POEMS-Syndrom." Medizinische Klinik 93, no. 11 (1998): 678–82. http://dx.doi.org/10.1007/bf03044880.

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4

Erbslöh-Möller, Brigitte, Boris Perras, and Klaus Sack. "POEMS-Syndrom mit Niereninsuffizienz." Medizinische Klinik 94, no. 3 (1999): 159–64. http://dx.doi.org/10.1007/bf03044846.

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5

Ebhardt, H., T. Eidner, A. Berndt, D. Katenkamp, and H. Kosmehl. "Das POEMS-Syndrom - Ein Fallbericht." Der Pathologe 21, no. 3 (2000): 255–59. http://dx.doi.org/10.1007/s002920050397.

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6

Mäurer, M., and C. Sommer. "POEMS-Syndrom - ungewöhnliche Manifestation mit beidseitigem Charcot-Gelenk." DMW - Deutsche Medizinische Wochenschrift 124, no. 12 (2008): 346–50. http://dx.doi.org/10.1055/s-2007-1024305.

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7

Schaumberg, J., C. Müller-Habich, and A. Müller-Jensen. "POEMS-Syndrom – schwierig zu diagnostizieren – schwierig zu therapieren." Aktuelle Neurologie 37, no. 02 (2010): 86–88. http://dx.doi.org/10.1055/s-0029-1223517.

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8

Birkenbach, A., F. Kühlhorn, M. Grube, H. Helbig, and M. A. Gamulescu. "POEMS-Syndrom als seltene Ursache eines bilateralen Papillenödems." Der Ophthalmologe 114, no. 3 (2016): 262–65. http://dx.doi.org/10.1007/s00347-016-0287-8.

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9

Kurzen, Kunz, and Nigg. "Blauverfärbung der Hände, Taubheitsgefühl an den Füssen, indolente Lymphknotenschwellung zervikal bei einem 73-jährigen Mann." Praxis 95, no. 41 (2006): 1589–93. http://dx.doi.org/10.1024/1661-8157.95.41.1589.

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Ein 73-jähriger Patient wurde uns zugewiesen wegen einer Blauverfärbung der Hände. Zusätzlich bestanden anamnestisch und klinisch eine B-Symptomatik, brennende Schmerzen mit Taubheitsgefühl an den Füssen bei Polyneuropathie sowie eine indolente Lymphknotenschwellung zervikal. 1996 und 2001 waren wegen einer lokalisierten angiofollikulären Lympknotenhyperplasie (Castleman-Erkrankung) bereits Halslymphknoten exzidiert worden. Laborchemisch bestanden erhöhte Entzündungszeichen, eine Hypothyreose und eine monoklonale Gammopathie. Die Bildgebung zeigte generalisierte Lymphknotenvergrösserungen zerv

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Barry, Jean-Cyriaque, Marc Gleichmann, and Helmut Wilhelm. "Beidseitige Papillenschwellung bei Polyneuropathie, Organomegalies Endokrinopathie, monoklonalen Proteinen und Hautveränderungen (POEMS-Syndrom)." Klinische Monatsblätter für Augenheilkunde 215, no. 07 (1999): 59–63. http://dx.doi.org/10.1055/s-2008-1034671.

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11

Ulas, Sevtap Tugce, and Süha Dasdelen. "Multizentrische Castleman-Erkrankung in Kombination mit Polyserositis und POEMS-Syndrom – Fallbericht und Übersichtsbeitrag." Der Internist 62, no. 7 (2021): 777–85. http://dx.doi.org/10.1007/s00108-021-01063-4.

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12

Dowker, A., B. Hermelin, and L. Pring. "A savant poet." Psychological Medicine 26, no. 5 (1996): 913–24. http://dx.doi.org/10.1017/s003329170003525x.

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SynopsisPoems by an individual with a diagnosis of Asperger's Syndrome were analysed and compared with those of a comparison poet. Though the savant poet performed less efficiently on formal language tests supposed to tap creativity, there were few differences between the two poets in regard to the poems' content and the use of various structural devices. The poems by the savant referred more often to aspects of self-analysis, while descriptions of people not related to the self were less frequent. Both poets made use of similes and metaphors. The results are discussed in terms of different mo

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13

Gutiérrez Araujo, Vianca, Esther Hernández Santos, and Luis Camacho Saavedra. "Síndrome de POEMS: a propósito de un caso." Horizonte Médico (Lima) 22, no. 3 (2022): e1561. http://dx.doi.org/10.24265/horizmed.2022.v22n3.10.

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Vaithy, Anandraj, Shanmugasamy K, Bhavani Bhavani, and Koteeswaran G. "Spectrum of Clinico-Pathological Profile of Poems Syndrome." Annals of Pathology and Laboratory Medicine 5, no. 6 (2018): A527–532. http://dx.doi.org/10.21276/apalm.1986.

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15

Valkova, Mirena, and Velina Guergueltcheva. "Polyneuropathy, organomegaly, endocrinopathy, m protein and skin changes syndrome (POEMS) – literature review." Bulgarian Neurology 25, no. 2 (2024): 51–54. https://doi.org/10.5281/zenodo.15358459.

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Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes syndrome (POEMS) is a rare paraneoplastic syndrome, associated with plasma cell dyscrasia. POEMS involves several clinical signs and symptoms with varying presentation. The first and most prominent of them is the subacute painful sensory and motor polyneuropathy. The diagnosis is based on Dispenzieri criteria (2017). Differential diagnosis involves chronic demyelinating polyneuropathy, amyloidosis, monoclonal gammopathy of undetermined significance, chronic hepatitis, Humman Immunodeficiency Virus and other paraneoplastic

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Kyle, Robert A. "POEMS Syndrome." Clinical Lymphoma 4, no. 3 (2003): 186. http://dx.doi.org/10.3816/clm.2003.n.030.

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17

Keddie, Stephen, and Michael P. Lunn. "POEMS syndrome." Current Opinion in Neurology 31, no. 5 (2018): 551–58. http://dx.doi.org/10.1097/wco.0000000000000610.

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18

Scarlato, Marina, and Stefano C. Previtali. "POEMS syndrome." Current Opinion in Neurology 24, no. 5 (2011): 491–96. http://dx.doi.org/10.1097/wco.0b013e328348e107.

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Kumar, Naresh, Deepak Rosha, Puneet Gupta, and Tarun Sharma. "POEMS Syndrome." Apollo Medicine 3, no. 3 (2006): 318–21. http://dx.doi.org/10.1016/s0976-0016(11)60219-6.

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Soubrier, Martin. "Syndrome POEMS." La Presse Médicale 36, no. 11 (2007): 1676–82. http://dx.doi.org/10.1016/j.lpm.2007.06.009.

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21

Marcant, P., L. Terriou, E. Boyle, P. Y. Hatron, and D. Staumont-Sallé. "Syndrome POEMS." Annales de Dermatologie et de Vénéréologie 146, no. 1 (2019): 82–85. http://dx.doi.org/10.1016/j.annder.2018.11.003.

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22

Leung, Nancy W. Y., Joseph C. K. Pang, and Christopher W. K. Lam. "Poems syndrome." Pathology 23, no. 2 (1991): 167–71. http://dx.doi.org/10.3109/00313029109060819.

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23

Dispenzieri, Angela. "POEMS Syndrome." Hematology 2005, no. 1 (2005): 360–67. http://dx.doi.org/10.1182/asheducation-2005.1.360.

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Abstract POEMS syndrome is defined by the presence of a peripheral neuropathy (P), a monoclonal plasma cell disorder (M), and other paraneoplastic features, the most common of which include organomegaly (O), endocrinopathy (E), skin changes (S), papilledema, edema, effusions, ascites, and thrombocytosis. Virtually all patients will have either sclerotic bone lesion(s) or co-existent Castleman’s disease. Not all features of the disease are required to make the diagnosis, and early recognition is important to reduce morbidity. Other names for the syndrome include osteosclerotic myeloma, Crow-Fuk

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Laurenti, L., and S. De Matteis. "POEMS syndrome." Drugs of the Future 33, no. 6 (2008): 543. http://dx.doi.org/10.1358/dof.2008.033.06.1209527.

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25

Caswell, R., T. Warner, A. Mehta, and L. Ginsberg. "POEMS syndrome." Practical Neurology 6, no. 2 (2006): 111–16. http://dx.doi.org/10.1136/jnnp.2006.089003.

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Dispenzieri, Angela. "POEMS syndrome." Blood Reviews 21, no. 6 (2007): 285–99. http://dx.doi.org/10.1016/j.blre.2007.07.004.

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27

Perniciaro, Charles. "POEMS syndrome." Seminars in Dermatology 14, no. 2 (1995): 162–65. http://dx.doi.org/10.1016/s1085-5629(05)80013-6.

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28

Dispenzieri, Angela, Taxiarchis Kourelis, and Francis Buadi. "POEMS Syndrome." Hematology/Oncology Clinics of North America 32, no. 1 (2018): 119–39. http://dx.doi.org/10.1016/j.hoc.2017.09.010.

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Jaccard, Arnaud. "POEMS Syndrome." Hematology/Oncology Clinics of North America 32, no. 1 (2018): 141–51. http://dx.doi.org/10.1016/j.hoc.2017.09.011.

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30

Arkhipov, I. E., I. Yu Vergunova, N. A. Malkova, and D. S. Korobko. "POEMS-syndrome." Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova 123, no. 7 (2023): 15. http://dx.doi.org/10.17116/jnevro202312307215.

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31

Kumar, Naresh, Deepak Rosha, Puneet Gupta, and Tarun Sharma. "Poems Syndrome." Apollo Medicine 3, no. 3 (2006): 318–21. http://dx.doi.org/10.1177/0976001620060312.

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32

Juan, Enrique Gutierrez Valencia, Cruz Cruz Alais, Alberto Fuentes-Lara Jesús, et al. "Fractionated Stereotactic radiotherapy for POEMS syndrome: A case report." International Journal of Medical Reviews and Case Reports 3, no. 1 (2018): 54–56. https://doi.org/10.5455/IJMRCR.poems-syndrome-fractionated-stereotactic-radiotherapy.

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Background: POEMS syndrome is a rare neoplastic entity. It has population incidence of 0.3/100,000 and presents predominantly on the 5th or 6th decade of life. Its treatment is considered to be multidisciplinary. Case summary: We present the case of a 47 year old male patient with POEMS syndrome who was initially managed with chemotherapy but was treated with stereotactic radiation therapy for spinal cord compression associated due to a plasma cell neoplasm at the T6-T7 vertebral body. Conclusion: Radiation therapy is the preferred treatment modality for one to three isolated bone lesions, wit

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Paolo Sotelo, Pedro, Fanny Elizabeth Ramírez Calderón, and María Del Pilar Quiñones Avila. "SÍNDROME POEMS ASOCIADO A ENFERMEDAD DE CASTLEMAN. UN REPORTE DE CASO." Revista de la Facultad de Medicina Humana 19, no. 4 (2019): 120–25. http://dx.doi.org/10.25176/rfmh.v19i4.2145.

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34

Wysocka-Dubielecka, Kalina, Andrzej Bizoń, Katarzyna Głogowska, et al. "Pseudoscleroderma associated with POEMS syndrome." Dermatology Review 106, no. 5 (2019): 529–37. http://dx.doi.org/10.5114/dr.2019.90001.

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Valencia, Juan, Alais Cruz, Jess FuentesLara, et al. "Fractionated Stereotactic radiotherapy for POEMS syndrome, a case report." International Journal of Medical Reviews and Case Reports 2, Reports in Surgery and Dermatolo (2019): 1. http://dx.doi.org/10.5455/ijmrcr.poems-syndrome-fractionated-stereotactic-radiotherapy.

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Del Río, R., M. Alsina, J. Monteagudo, et al. "POEMS syndrome and multiple angioproliferative lesions mimicking generalized histiocytomas." Acta Dermato-Venereologica 74, no. 5 (1994): 388–90. http://dx.doi.org/10.2340/0001555574388390.

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A case of POEMS syndrome and Castleman's multicentric disease is reported. Multiple long-standing cutaneous lesions, histologically similar to histiocytomas, were the initial manifestation of POEMS syndrome. A high incidence of angiomatous lesions associated with POEMS syndrome has already been established. To our knowledge, this report is the first report to associate multiple angioproliferative lesions mimicking generalized histiocytomas with POEMS syndrome.

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Rose, C., M. Mahieu, E. Hachulla, et al. "Le POEMS syndrome." La Revue de Médecine Interne 18, no. 7 (1997): 553–62. http://dx.doi.org/10.1016/s0248-8663(97)80807-7.

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Ding, Chao, and Yanqiu Li. "A case of paraprotein-negative POEMS syndrome: Case report and literature review." Medicine 103, no. 36 (2024): e39267. http://dx.doi.org/10.1097/md.0000000000039267.

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Rationale: POEMS syndrome is a rare monoclonal plasma cell disease. The diagnosis of POEMS requires polyradiculoneuropathy and monoclonal plasma proliferating as 2 mandatory criteria, at least 1 of the major criteria (Castleman disease, elevated vascular endothelial growth factor level, and sclerotic bone lesion), and at least 1 of the minor criteria (organomegaly, extravascular volume overload, endocrinopathy, skin changes, papilledema, and thrombocytosis/polycythemia). This multisystem disorder is of high heterogeneity, and few variants of POEMS with no evidence of monoclonal gammopathy have

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Dörner, Marc, Mihai Ceanga, Frank Schreiber, et al. "High-Resolution Nerve Ultrasound Abnormalities in POEMS Syndrome—A Comparative Study." Diagnostics 11, no. 2 (2021): 264. http://dx.doi.org/10.3390/diagnostics11020264.

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Background: High-resolution nerve ultrasound (HRUS) has been proven to be a valuable tool in the diagnosis of immune-mediated neuropathies, such as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes) is an important differential diagnosis of CIDP. Until now, there have been no studies that could identify specific HRUS abnormalities in POEMS syndrome patients. Thus, the aim of this study was to assess possible changes and compare findings with CIDP patients. Methods: We retrospectively analyzed

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Ueda, Shuji, Sayoko Yonemoto, Kazumasa Oka, et al. "Lenalidomide and Dexamethasone for a Patient of POEMS Syndrome Presenting with Massive Ascites." Case Reports in Hematology 2014 (2014): 1–3. http://dx.doi.org/10.1155/2014/818946.

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POEMS syndrome is a multisystem disorder characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes. POEMS syndrome is a rare cause of refractory ascites. We report the case of a patient with POEMS syndrome presenting with massive ascites who was treated with very-low-dose lenalidomide and dexamethasone. A 57-year-old Japanese man was admitted to our hospital with pleural effusion, massive ascites, and leg edema. The diagnosis of POEMS syndrome was made based on the combination of the following findings: peripheral neuropathy, organomegaly, endocrino

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Korotaeva, V. V., Ya B. Kushnir, O. V. Kudyasheva, A. Yu Polushin та V. S. Krasnov. "POEMS-syndrome with the disease onset in the form of сhronic dysimmune neuropathy". Russian Medical Inquiry 6, № 10 (2022): 589–95. http://dx.doi.org/10.32364/2587-6821-2022-6-10-589-595.

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POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, M-protein, Skin changes) is a rare paraneoplastic disease associated with plasma cell dyscrasias, the pathogenesis of which is currently not fully understood. The diagnosis of POEMS syndrome is commonly confirmed after an extended period of time from the disease onset, since the syndrome is rare and can be mistaken for other neurological diseases, for instance, chronic inflammatory demyelinating polyneuropathy (CIDP). The article describes a clinical case of the disease in a young male patient with the onset of neurological disorder

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Bhattacharjee, S., I. Siyad, and BV Maramattom. "Chronic diarrhea - The poetic masquerade." Journal of Postgraduate Medicine 68, no. 4 (2022): 239–42. http://dx.doi.org/10.4103/jpgm.jpgm_1169_21.

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Chronic diarrhea, by definition, is the passage of loose/liquid stools, with increased frequency (more than three times/day), or an output of over 200 g/day, lasting for a duration of four or more weeks. The clinical approach to identify the cause of chronic diarrhea generally depends on the local socioeconomic status. In high-income countries, systemic causes such as irritable bowel syndrome (IBS), inflammatory bowel disease, malabsorption syndromes (lactose intolerance/coeliac disease) are primarily considered. In mid- to low-income countries, infective causes like chronic bacterial, mycobac

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Shi, Huan, Xiaohong Jiang, Long Wang, and Jiayan Zhou. "Missed diagnosis of POEMS syndrome with onset of progressive fatigue and numbness: a case report." Journal of International Medical Research 49, no. 2 (2021): 030006052098670. http://dx.doi.org/10.1177/0300060520986706.

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POEMS syndrome is a rare multisystem disease associated with an underlying plasma cell disorder. Its name is an acronym for peripheral neuropathy (P), endocrinopathy (E), organomegaly (O), monoclonal plasma cell proliferative disorder (M), and skin changes (S). This case report describes a patient with POEMS syndrome who presented with progressive fatigue and numbness in the lower extremities. Initially, the patient was erroneously diagnosed with diabetes and diabetic peripheral neuropathy because of the endocrinopathy associated with POEMS syndrome. After a second hospitalization, the patient

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Aguilar-Vázquez, Crhistian Alejandro, and Nallely Denisse Ruvalcaba-Sánchez. "Síndrome de POEMS. Reporte de tres casos y revisión de literatura." Revista Médica del Instituto Mexicano del Seguro Social 62, no. 4 (2024): e5666. https://doi.org/10.5281/zenodo.11397295.

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<strong>Resumen</strong> <strong>Introducción: </strong>el síndrome de POEMS es un trastorno paraneoplásico incapacitante, relacionado con una neoplasia de células plasmáticas. Clínicamente se caracteriza por neuropatía periférica de predominio desmielinizante y muchas veces inicia en miembros pélvicos, organomegalia, endocrinopatía, cambios en la piel y proteína M sérica elevada. Para el diagnóstico se requiere cumplir un conjunto de criterios clínicos en los que la polirradiculoneuropat&iac

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Liang, Minrui, Zhixing Jiang, Zhiguang Lin, et al. "Polyneuropathy as Novel Initial Manifestation in a Case of “Nonsecretory” POEMS Syndrome with Sjögren’s Syndrome." Case Reports in Medicine 2017 (2017): 1–6. http://dx.doi.org/10.1155/2017/1276759.

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POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) is a paraneoplastic syndrome driven by plasma cell dyscrasias. We report a patient with novel initial manifestation of polyneuropathy, which was considered due to Sjögren’s syndrome but with poor response to methylprednisolone (120 mg/d) and intravenous immunoglobulin (IVIg). Further investigation by imaging tests and following biopsy eventually confirmed the diagnosis of POEMS syndrome secondary to solitary plasmocytoma. To our knowledge, this is the first reported case of POEMS syndrome wit

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Rathore, Hemant, and Nirav Thaker. "Chronic Inflammatory Demyelinating Polyradiculoneuropathy as a Presentation of Plasmacytoma." Indian Journal of Nuclear Medicine 38, no. 4 (2023): 379–80. http://dx.doi.org/10.4103/ijnm.ijnm_44_23.

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Polyneuropathy, organomegaly, endocrinopathy, M protein elevation, and skin changes (POEMS) syndrome is one of the rare paraneoplastic disorders of the multiorgan association whose initialism describes the principal clinical features as polyneuropathy, organomegaly, endocrinopathy, M-protein elevation, and skin changes caused by an underlying plasma cell disorder, one of the major diagnostic criteria for which is the presence of an osseous lesion. We present a case of POEMS syndrome with nearly all signs and symptoms on clinical and hematological examinations, which was further investigated wi

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Du, Hua Ping, Ye Zhang, Lei Min Sun, and Liang Luo. "Two cases of special POEMS syndrome without monoclonal protein expression: a case report and literature review." Journal of International Medical Research 49, no. 4 (2021): 030006052199096. http://dx.doi.org/10.1177/0300060521990967.

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POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, skin changes) syndrome is rare, with polyneuropathy and monoclonal plasma cell disorder generally considered as essential diagnostic symptoms. We report two cases of POEMS syndrome without monoclonal protein expression. The first case was a 72-year-old man who had experienced recurrent edema of the lower limbs for 2 years and abdominal distention for 2 months. The other case was a 62-year-old man with a 5-year history of recurrent numbness of the extremities and muscle weakness, which had become serious over the preceding

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Casacov, Rolando, Oscar Díaz Moyano, and Mercedes Cassino. "Sindrome de Poems." Revista de la Facultad de Ciencias Médicas de Córdoba 56, no. 2 (2023): 113–21. http://dx.doi.org/10.31053/1853.0605.v56.n2.40331.

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Poems syndrome :s a rare multisistemic disorder. It manifestations are Polynueropathy, Organomegaly, Endocrinopathy,and / 01Edema. Monoclonal protein and changes in the Skin. (P.O.E.M.S.)Though some bibliography make no difference with osteoesclerotic mieloma it is considered a real syndrome.The polynueropathy is customarily severe. Although high levels of inrnullo- globulins has been found in the poems, it has not been isolatcd a specific antibody that explain the polynueropathy even though it is strongly suspected.The organomegaly, endocrinopathy, changes in the skin and other systems and in

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Valkova, Mirena, Elena Tzolova, and Velina Guergueltcheva. "Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes syndrome (POEMS) – case report." Bulgarian Neurology 25, no. 2 (2024): 77–78. https://doi.org/10.5281/zenodo.15360454.

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Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes syndrome (POEMS) is a rare paraneoplastic syndrome, associated with plasma cell dyscrasia. We present a clinical case of POEMS syndrome with specific subacute painful polyneuropathy, weight loss, diarrhea, edema, JAK2 negative polycythemia and Mprotein.Conclusion: POEMS should be considered incases with specific subacute painful sensory and motor polyneuropathy and characteristic bone lesions or skin changes.

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Bourgeault, Emilie, Alice Dahl, Marie-Marthe Thibeault, Audrey Dupéré, Anne-Marie Drolet, and Jean Mathieu. "POEMS Syndrome Complicated by Extensive Calciphylaxis: A Remarkable Recovery." Journal of Cutaneous Medicine and Surgery 19, no. 3 (2015): 309–12. http://dx.doi.org/10.2310/7750.2014.14086.

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Background and Objective Calciphylaxis is life threatening. It has traditionally been associated with end-stage renal disease and hyperparathyroidism but is increasingly common in other clinical contexts. The association of polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome and calciphylaxis has been reported only in a few cases. This case is the first of patient survival in such widespread disease. Methods and Results A 42-year-old man with POEMS syndrome developed extensive calciphylaxis despite normal renal and parathyroid function. Rapid

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