Extractions: Volumen 12, número 3, 2003 Página principal Presentación Equipo directivo y comité científico Información para los autores ... Congreso virtual de neurología Síndrome de POEMS: Múltiples manifestaciones clínicas durante su larga evolución. Dra. Rocío Santibáñez, Dr. Jorge Astudillo, Dr. Enrique Díaz-Calderón, Dr. Rafael Aguirre. Servicio de Neurología Hospital Regional Dr. Teodoro Maldonado Carbo Guayaquil, Ecuador Correspondencia: Dra. Rocío Santibáñez, Casilla 09-04-462 Policentro, Guayaquil, Ecuador RESUMEN: ABSTRACT: Being a multisystemic disorder, POEMS syndrome has different clinical features.and comprises multiple organs. The referred acronym: polyneuropathy, organomegaly, endocrinopathy, monoclonal protein M and skin changes, results insufficient when this syndrome is described, because of the constellation of multiple signs and symptoms. Neurologically a chronic demyelinating peripheral neuropathy is the common clinical presentation, which is associated with an osteosclerotic myeloma in 50% of cases. Involvement of central nervous system includes papilledema and intracraneal hypertension, less frequently. We report a patient with POEMS syndrome with 11 years follow-up, who has recently developed intracraneal hypertension features. We discuss clinical findings and review literature.
DBGET Result: OMIM 192240 POEMS syndrome, also known as crowfukase syndrome (Crow, 1956; Shimpo, 1968),is a rare multisystem disorder of obscure pathogenesis and no conspicuous http://www.genome.jp/dbget-bin/www_bget?omim 192240
C Health, Directory Chondromalacia crowfukase syndrome Crohn s Disease Canavan Disease Crigler-Najjar Syndrome Chlamydia Cubital Tunnel Syndrome Colibacillosis http://www.lila-ilab.org/bGlfNDMzNDU=.aspx
?-www.sunbinmd.com Translate this page M-proteinand skin changes the POEMS syndrome. Medicine(Baltimore) 1980,59(4)3118 Nakanishi T Sobue I, Toyokura Y, et al. The crow-fukase syndrome http://www.sunbinmd.com/newsinfo.asp?nid=93
I-une.com: Conditions And Diseases > C Craniosynostosis@ (); Creutzfeldt Jakob Disease@ (); Cri du Chat Syndrome@ ();CriglerNajjar Syndrome@ (); Crohn s Disease@ (); crow-fukase syndrome@ http://dir.i-une.com/Health/Conditions_and_Diseases/C/
Health/Conditions And Diseases/C -- The Doctors Lounge(TM) CriglerNajjar Syndrome@ 4; Crohn s Disease@ 100; crow-fukase syndrome@ 2;Cryptorchidism@ 2; Cryptosporidiosis@ 10; Cubital Tunnel Syndrome@ 6 http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/C/index.cgi
MYOM2 - Myomesin 2 POEMS/crowfukase syndrome is a rare multisystem disorder associated with elevatedvascular endothelial growth factor ( VEGF), which clinically presents http://www.pdg.cnb.uam.es/UniPub/iHOP/gg/94437.html
a\ Yodoi J, Uchino H, Takatsuki K. Report of a patient with POEMS/Takatsukicrowfukase syndrome associated with focal pachymeningeal amyloidosis. http://www.kuhp.kyoto-u.ac.jp/~pathology/gyoseki_eigo.html
Extractions: 1980Niºa55Nj 1. Ichijima K, Yamabe H, Kobashi Y, Fujii Y, Inoue Y. Peliosis hepatis. An unusual case involving multiple organs. Acta Pathol Jpn 1980; 30: 109-120. 2. Ichijima K, Yamabe H, Kobashi Y, Iwata T. Metastasis of cancer to cancer. Acta Pathol Jpn 1980; 30: 293-300. 3. Nakashima Y, Hirose S, Hamashima Y. Proliferation of cultured rabbit renal glomerular cells stimulated by platelet factor. Acta Pathol Jpn 1980; 30:1-7. 4. Nakashima Y, Hirose S, Hamashima Y. Acid phosphatase activity in cultured rabbit renal glomerular cells. Acta Histochem Cytochem 1980; 13:211-217. 1981Niºa56Nj 5. Ichijima K, Yamabe H, Kobashi Y, Ogawa H, Akaishi K. An unusual case of metaphyseal chondrodysplasia with an abnormal perilacunar matrix associated with agranulocytosis and hypoplasia of the thymus. Virchows Arch A (Pathol Anat) 1981; 391: 275-289. 6. Ohtsuki H, Haebara H, Takahashi K, Midorikawa O, Tomoyoshi E, Torii S, Miura K. Aicardi's syndrome: report of an autopsy case. Neuropediatrics 1981; 12: 279-286. 7. Yamashita J, Handa H, Morimoto M, Oda Y, Nakashima Y. Xanthomatous meningioma. J Comput Assist Tomogr 5:272-273, 1981.
NEJM -- Sign In The two central features of the crowfukase syndrome are the The most frequentinitial findings in the crow-fukase syndrome25 are related to the http://content.nejm.org/cgi/content/full/328/21/1550
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ãw¤È@¤ÒÊ Translate this page vascular endothelial growth factor in platelets in crow-fukase syndrome. permeability factor is causative in Crow-Fukase (POEMS) syndrome. http://www.kufm.kagoshima-u.ac.jp/~md-io/staff/ArimuraK.html
Extractions: Clinical aspects of Minamata disease: neurological manifestations as seen in Minamata disease patients and in residents of methylmercury-polluted areas. Understanding of Minamata disease. Methymercury Poisoning in Minamata and Niigata, Japan. Edited by Yakizawa Y and Osame M. Japan Public Health Association. pp51, 2001
Special Topics Myelin And Myelination Bibliographic Database Diet, lipids and brain development; crowfukase syndrome; Animal Models forInherited Peripheral Neuropathies Chances to Find Treatment Strategies? http://csa.tsinghua.edu.cn/csa/e_products/bacontent/NEU000223.html
gbvy[W Yaguchi H, Tsuboi R, Ogawa H. 3, A case of crowfukase syndrome. 20th WorldCongress of Dermatology, Paris (2002.6.30-7.5), Ichikawa M , Okita M, Oh-iT http://www.tokyo-med.ac.jp/derma/gyouseki/i_ippan/i_ippan.htm
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POEMS Syndrome Synonyms, Eastern Carolina POEMS Syndrome Synonyms University Health Systems of Eastern Carolina servestarboro, ahoskie, edento, winsor, crow-fukase syndrome; PEP Syndrome http://www.uhseast.com/113927.cfm
Extractions: It is possible that the main title of the report POEMS Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. POEMS syndrome is an extremely rare multisystem disorder. POEMS is an acronym that stands for (P)olyneuropathy, disease affecting many nerves; (O)rganomegaly, abnormal enlargement of an organ; (E)ndocrinoapthy, disease affecting certain hormone-producing glands that help to regulate the rate of growth, sexual development, and certain metabolic functions (endocrine system); (M)onoclonal gammopathy or M proteins; and (S)kin defects. Common symptoms include progressive weakness of the nerves in the arms and legs, an abnormally enlarged liver and/or spleen (hepatosplenomegaly), abnormally darkening of the skin (hyperpigmentation) and excessive hair growth (hypertrichosis). Endocrine abnormalities such as failure of the ovaries and testes (gonads) to function properly (primary gonadal failure) and diabetes mellitus type I may be present. Specific endocrine abnormalities associated with POEMS syndrome vary from case to case.
Masson The Racand syndrome is associated with pulmonary hypertension. P1030. Chilblain lupuserythematosus in the A case of crowfukase syndrome. P1074 http://www.e2med.com/sync/cdRoms/wcd2002/mso0017.htm
Extractions: HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS This Article Abstract Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Cited by other online articles PubMed PubMed Citation Articles by LESPRIT, P. Articles by GHERARDI, R. Am. J. Respir. Crit. Care Med., Volume 157, Number 3, March 1998, 907-911 Pulmonary Hypertension in POEMS Syndrome REFERENCES POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) syndrome is a rare variant of plasma cell dyscrasia with multiple systemic manifestations. We followed the progress of 20 patients with POEMS syndrome in our institution over a 10-yr period. Pulmonary hypertension (PH) was
