Arch Dermatol -- Table Of Contents (Vol. 123 No. 4, April 1987) 1987;123424. Systemic plasmacytosis and the crowfukase syndrome JL Burton Arch Dermatol. 1987;123425-426. Pityriasis rotunda a dermatophytosis? http://archderm.ama-assn.org/content/vol123/issue4/index.dtl
Arch Dermatol -- Abstracts: Shelley And Shelley 123 (1): 85 Discovery of a plasma cell tumor led to recognition of the crowfukase syndrome, and appropriate treatment with melphalan and prednisone. http://archderm.ama-assn.org/cgi/content/abstract/123/1/85
Extractions: Vol. 123 No. 1, January 1987 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Shelley WB Shelley ED Contact me when this article is cited W. B. Shelley and E. D. Shelley A man with a six-year history of intermittent burning sensations in his legs, hypothyroidism, and peripheral neuropathy also had hypertrichosis, hyperpigmentation, Terry nails, and taut thickened skin of the extremities. Discovery of a plasma cell tumor led to recognition of the Crow-Fukase syndrome, and appropriate treatment with melphalan and prednisone.
C From Linkspider UK Health Directory Jakob Disease; Cri du Chat Syndrome; CriglerNajjar Syndrome; Crohn s Disease; crow-fukase syndrome; Cryptorchidism; Cryptosporidiosis; http://linkspider.co.uk/Health/ConditionsandDiseases/C/
Extractions: Match » -All words -Any word -Exact text Search » The Web Jobs / Vacancy Images / Photos FTP / Downloads United Kingdom United States of America Argentina Austria Australia Bangladesh Belgium Bolivia Brazil Bulgaria Canada Chile China Cuba Cyprus Czech Republic Czechoslovakia Denmark Dominican Republic Ecuador Egypt Estonia Finland France Germany Ghana Greece Hong Kong Hungary Iceland India Indonesia Ireland Israel Italy Japan Jordan Kenya Kuwait Latvia Lithuania Luxembourg Malaysia Malta Mexico Moldavia Monaco Morocco Mozambique Nepal Netherlands New Zealand Nicaragua Nigeria North Korea Norway Pakistan Panama Paraguay Peru Philippines Poland Portugal Qatar Romania Russian Federation Saudi Arabia Singapore South Africa South Korea Spain Sri Lanka Sweden Switzerland Taiwan Tanzania Thailand Tunisia Turkey Ukraine United Arab Emirates Uruguay Venezuela Yemen Yugoslavia Zambia Zimbabwe Ranking » On (no duplicate) Off (allow duplicate) Add my Site Toolbar Affiliates Campylobacter Pylori Canavan Disease Cancer Candida ... Cytomegalovirus
Shinshu University Faculty Of Arts Browser[Ryuzo Nitta] crowfukase syndrome - immunoadsorption plasmapheresis effectively lowers elevated interleukin-6 concentration. Nephrol Dial Transplant Vol.14, pp.419 http://www.shinshu-u.ac.jp/souran/menu/gakubu-e/byoinb/byoink/fnaika2/higuchi.ht
Health Conditions And Diseases C 10 Creutzfeldt Jakob Disease@ 30 Cri du Chat Syndrome@ 5 CriglerNajjar Syndrome@ 3 Crohn s Disease@ 103 crow-fukase syndrome@ 2 Cryptorchidism@ 2 http://www.pastconnect.com/odp/directory/Health/Conditions_and_Diseases/C/
Chest -- Mokhlesi And Jain 115 (6): 1740 POEMS (polyneuropathy, organomegaly, endocrinopathy, Mprotein spike, and skin changes) syndrome, also known as Takatsuki-crow-fukase syndrome, was first http://www.chestjournal.org/cgi/content/full/115/6/1740
Health- Conditions And Diseases- C Najjar Syndrome@ (3); Crohn s Disease@ (103); crowfukase syndrome@ (2); Cryptorchidism@ (2); Cryptosporidiosis@ (10); Cubital Tunnel http://iasweb.com/ODP/Health/Conditions_and_Diseases/C/
Open Directory - Health: Conditions And Diseases: C Najjar Syndrome@ (5); Crohn s Disease@ (195); crowfukase syndrome@ (2); Cryptorchidism@ (2); Cryptosporidiosis@ (6); Cubital Tunnel http://dmoz.com/Health/Conditions_and_Diseases/C/
Health Conditions And Diseases C Najjar Syndrome @ (3); Crohn s Disease @ (103); crowfukase syndrome @ (2); Cryptorchidism @ (2); Cryptosporidiosis @ (10); Cubital Tunnel http://freshlinks.net/odp.aspx/Health/Conditions_and_Diseases/C/
Descipher™ - Disease And Condition Index - C Jakob dementia CreutzfeldtJakob disease CRF Crigler-Najjar syndrome crisis, celiac Crohn s disease croupous bronchitis crow-fukase syndrome cruris, tinea http://www.descipher.com/argo/diseases/c/
C Site Information At B2bYellowpages.com - Business To Business Najjar Syndrome@ (5); Crohn s Disease@ (100); crowfukase syndrome@ (2); Cryptorchidism@ (2); Cryptosporidiosis@ (6); Cubital Tunnel http://b2byellowpages.com/web.cgi/Health/Conditions_and_Diseases/C/
Extractions: Clinical manifestations of 102 cases with the Crow- Fukase syndrome (the syndrome of polyneuropathy, anasarca, skin changes, endocrinopathy, dysglobulinemia, and organomegaly), with or without myeloma, were reviewed. Fifty-six cases with myeloma consisted of 31 with osteosclerotic, 17 with mixed osteosclerotic and osteolytic, and 8 with osteolytic. Forty-six cases without myeloma consisted of 2 with extramedullary plasmacytoma, 33 with M protein alone, and 11 with polyclonal protein alone. There was no
MASSON Editeur P1073. A case of crowfukase syndrome. P1074. Serum leptin levels are increased in Behçet disease. P1075. Poikiloderma atrophicans vasculare-dermatomyositis. P1076. http://www.e2med.com/sync/cdRoms/wcd2002/mso0017.htm
Extractions: Clinical and prognostic associations of anti-topoisomerase I antibody in systemic sclerosis Elevated levels of soluble HLA in the saliva of patients with severe collagen vascular disease Eruptive skin vascular tumors associated with graft versus host disease Cutaneous findings in thirty-seven patients with chronic lymphocytic leukaemia ... The erythemateous lupus in children
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.
ORPHANET - Maladies Rares - Médicaments Orphelins Translate this page Glossaire, Version pour Impression, MALADIE POEMS syndrome, Synonyme(s) crow-fukase, syndrome de, Aucun descriptif disponible, Signes cliniques(23), http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=2905
POEMS Translate this page POEMS. Voir également Castleman (tumeur ou maladie de),. En anglais POEMS syndrome. Synonymes syndrome de crow-fukase, syndrome de Takatsuki. http://www.vulgaris-medical.net/textp/poems.html
Extractions: Syndrome (association de symptômes) rare dont l'origine est inconnue et qui a tout d'abord été décrit au Japon. Il se caractérise par une neuropathie (atteinte du système nerveux) périphérique (à différencier du système nerveux central regroupant le cerveau, le cervelet et la moelle épinière entre autres). Symptômes Il montre une dysglobulinémie monoclonale. La dysglobulinémie est une maladie rencontrée parfois chez le sujet âgé ou chez certains malades présentant une atteinte du système lymphoïde (rate, thymus, ganglions, organes lymphoïdes), une maladie auto-immune (le malade fabrique des anticorps contre ses propres tissus) ou une cirrhose du foie. Cette pathologie inconnue peut frapper 2 à 3 % de la population de plus de 70 ans. Elle est causée par la présence d'une certaine quantité de protéines anormales dans le sang. Ce sont des anticorps (immunoglobulines) provenant dune lignée unique, appelés également clones de cellules plasmocytaires. Les plasmocytes sont issus dune variété de globules blancs fabriqués dans la moelle osseuse.
