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         Crow-fukase Syndrome:     more detail

61. 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
Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA For The Media Classified Ads Meetings Peer Review Congress
Vol. 123 No. 4, pp. 424-536, April 1987 Content Access Register Subscribe One-time Access E-mail Alerts Table of Contents Jump to Section ARTICLES
ARTICLES Antibiotic prophylaxis and dermatologic surgery
B. Lycka
Arch Dermatol.
Acral erythema: graft-vs-host disease or toxicoderma?
E. Martin-Ortega; J. Palou; J. M. Mascaro; J. M. Marti; A. Granena
Arch Dermatol.
Systemic plasmacytosis and the Crow-Fukase syndrome
J. L. Burton
Arch Dermatol. Pityriasis rotunda: a dermatophytosis? A. D. Lewis Arch Dermatol. Actinomycetoma caused by Nocardiopsis dassonvillei L. Ajello; J. Brown; E. Macdonald; E. Head Arch Dermatol. Cryotherapy of psoriasis R. B. Scoggins Arch Dermatol. Anthralin minute entire skin treatment: a follow-up and comparison with methoxsalen plus ultraviolet light P. Duschet; T. Schwarz; M. Pusch; A. Wagner; F. Gschnait

62. 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
Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA For The Media Classified Ads Meetings Peer Review Congress
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
The skin changes in the Crow-Fukase (POEMS) syndrome. A case report
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.
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63. C From Linkspider UK Health Directory
Jakob Disease; Cri du Chat Syndrome; CriglerNajjar Syndrome; Crohn s Disease; crow-fukase syndrome; Cryptorchidism; Cryptosporidiosis;
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64. 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
Makoto Higuchi
Assistant, M.D., Ph.D Second Department of Internal Medicine E-mail : mhiguchi@hsp.md.shinshu-u.ac.jp Phone : + Fax : +
Academic Background Niigata University School of Medicine, 1986
Assistant since 1999 Research and Educational Interests Clinical and experimental Nephrology, Microcirculation
Clinical investigation of IgA nephropathy
Role of macrophage in primary glomerulonephritis and diabetic
nephropathy
key words: nephrology, macrophage, diabetic nephropathy Selected Publications
  • "Plasma exchange with concurrent hemodiafiltration saved two patients with fulminant hepatitis." Therapeutic Plasmapheresis (IX) Vol.318, pp.353-356 (1991)
  • "Effects of pravastatin on serum lipids and apolipoproteins in hyperlipidemia of the nephrotic syndrome." Jpn J Nephrol Vol.34(4) ,pp.397-403 (1992)
  • "A case of cryoglobulinemia accompanied by macroglobulinemia during long-term double filtration plasmapheresis. Therapeutic Plasmapheresis (X) Vol.321, pp.422- 426 (1992)
  • "Benefical effect of dibutyryl cyclic AMP (DbcAMP) on ischemic acute renal failure." Renal Failure Vol.14(4), pp.461-465 (1992)
  • 65. 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
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    66. 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
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    Download to Citation Manager Chest. American College of Chest Physicians
    Pulmonary Manifestations of POEMS Syndrome
    Case Report and Literature Review
    Babak Mokhlesi , MD and Manu Jain , MD From the Division of Pulmonary and Critical Care, Department of Medicine, Northwestern University Medical School, Chicago, IL. Abstract TOP Abstract Introduction Case Report Discussion References Phrenic nerve paresis is an unusual complication of POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein spike and skin changes) syndrome. In this report, we describe a case of POEMS syndrome in

    67. Health- Conditions And Diseases- C
    Najjar Syndrome@ (3); Crohn s Disease@ (103); crowfukase syndrome@ (2); Cryptorchidism@ (2); Cryptosporidiosis@ (10); Cubital Tunnel
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  • 68. Open Directory - Health: Conditions And Diseases: C
    Najjar Syndrome@ (5); Crohn s Disease@ (195); crowfukase syndrome@ (2); Cryptorchidism@ (2); Cryptosporidiosis@ (6); Cubital Tunnel
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  • 69. Health Conditions And Diseases C
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  • 70. Descipher™ - Disease And Condition Index - C
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    71. C Site Information At B2bYellowpages.com - Business To Business
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    72. Neurology -- Abstracts: Nakanishi Et Al. 34 (6): 712
    Neurology, Vol 34, Issue 6 712720, Copyright © 1984 by American Academy of Neurology. ARTICLES. The crow-fukase syndrome a study of 102 cases in Japan.
    http://intl.neurology.org/cgi/content/abstract/34/6/712
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    ARTICLES
    The Crow-Fukase syndrome: a study of 102 cases in Japan
    T Nakanishi, I Sobue, Y Toyokura, H Nishitani, Y Kuroiwa, E Satoyoshi, T Tsubaki, A Igata and Y Ozaki
    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

    73. MASSON Editeur
    P1073. A case of crowfukase syndrome. P1074. Serum leptin levels are increased in Behçet disease. P1075. Poikiloderma atrophicans vasculare-dermatomyositis. P1076.
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    74. POEMS SYNDROME
    Name. POEMS SYNDROME Synonyms. crowfukase syndrome (codes). pep syndrome (pigmentation, oedema, plasma cell dyscrasia) (codes). polyneuropathy
    http://malattierare.pediatria.unipd.it/pubblicaMR/mr_dx_ing.asp?mr=274

    75. Dorlands Medical Dictionary
    crowfukase syndrome (Crow-Fu·ka·se syndrome) (kro-foo-kah¢se) RS Crow, British physician, 20th century; Masaichi Fukase, Japanese physician, 20th century
    http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

    76. Síndrome De POEMS: Múltiples Manifestaciones Clínicas Durante Su Larga Evoluc
    Coagulation and vascular abnormalities in crow-fukase syndrome.
    http://www.medicosecuador.com/revecuatneurol/vol12_n3_2003/poems.htm
    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.

    77. ~CR // Medical-Conditions.org // Medical Conditions
    Virus Croup Associated Viruses CroupAssociated Virus Croup-Associated Viruses Crouzon Disease Crouzons Disease Crow Crow Fukase Syndrome crow-fukase syndrome
    http://www.medical-conditions.org/?q=~Cr

    78. ?
    5) crowfukase syndrome (Takatsuki disease, osteosclerotic myeloma, POEMS*). *polyneuropathy, organomgaly, endocrinopathy, M protein, and skin changes.
    http://www.showa.gunma-u.ac.jp/~hmura/mm-diagnosis.htm
    œ‘Žîf—‚ÌŽèˆø‚« i‰”Łj ”N ŒQ”n‘åŠwˆãŠw•”•ÛŒ¯Šw‰È ‘ºã”Ž˜a
    ‡T @œ‘Žî‚́A‹ß”NlŒû‚̍‚—‚É”º‚¢Š³ŽÒ”‚Í‘‰Á‚µ‚Ä‚¨‚èA‚»‚ÌŽ€–S—¦i‘ΐlŒû –œlj‚à ”N‚Ì l‚©‚ç ”N‚Ì l‚Æ monoclonal gammopathy monoclonal gammopathy ‚ð’æ‚·‚é•a‘ԁEŽ¾Š³‚É‚Í ˆÈ‰º‚ªŠÜ‚Ü‚ê‚éB j Monoclonal gammopathy of undetermined significance (MGUS) j Multiple myeloma Indolent myeloma Smoldering myeloma j Macroglobulinemia (Waldenstrom) j Heavy chain disease j Crow-Fukase syndrome (Takatsuki disease, osteosclerotic myeloma, POEMS*) *polyneuropathy, organomgaly, endocrinopathy, M protein, and skin changes ‡U œ‘Žî×–E‚Æ‚Í @œ‘Žî×–E‚́Aœ‘Œ`Ž¿×–E‚ª’PƒNƒ[ƒ“«‚É‘B‚µ‚½‚à‚Ì‚Æ‚³‚ê‚Ä‚«‚½B‚µ‚©‚µAÅ‹ßœ‘ŽîŠ³ŽÒ‚Ì––½ŒŒ’†‚ɍœ‘Žî‘O‹ì×–Ei precursor cell) ‚ª‘¶Ý‚·‚邱‚Æ‚ªŽ¦´‚³‚ê‚Ä‚¨‚èA‚Ü‚½‚±‚Ì precursor cell precursor cell ‚ðŒŸo‚·‚é•û–@‚Æ‚µ‚ẮAR idiotype R‘Ì‚É‚æ‚é–ƉuŠw“I•û–@A flowcytometry DNA complementarity determining region-3(CDR3) ‚ð—p‚¢‚½‰ðÍ–@‚È‚Ç‚ª‚ ‚éB‚±‚ê‚ç‚ÌŒ‹‰ÊAŒ»Ý‚Å‚Í B ×–E‚â pre-B ×–E‚ªœ‘ŽîƒNƒ[ƒ“‚É‘®‚µ‚Ä‚¢‚邱‚Æ‚ª•ª‚©‚Á‚Ä‚¢‚éB ‡V @œ‘Žî‚̏Ǐó‚́Aœ‘Žî×–EŽ©‘Ì‚Ì‘B‚É‚æ‚éÇóiŒŒ‹…Œ¸­AŒ`Ž¿×–EŽî‚Ȃǁj‚ƍœ‘Žî×–E‚ÌŽY¶‚·‚é—lX‚È•¨Ž¿iƒÁ ƒOƒƒuƒŠƒ“AƒTƒCƒgƒJƒCƒ“‚Ȃǁj‚É‚æ‚éÇó‚É‚Q‘å•Ê‚³‚ê‚éB ’J“à “y‰®‚ç —áj ’ɂ݁i˜E‹¹EŽlŽˆE”w•”’Ɂj •nŒŒÇói‚ß‚Ü‚¢E“®œ§‚Ȃǁj ”­”M oŒŒÇó “ª’ɁE“ªdŠ´ _ŒoÇóiˆÓŽ¯áŠQE‰^“®E’mŠoáŠQA‚µ‚Ñ‚ê‚Ȃǁj ‹ô‘R”­Œ©—á ‡W f’fŠî€ Diagnostic Criteria of Multiple Myeloma Major criteria I. Plasmacytoma on tissue biopsy

    79. 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

    80. 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
    POEMS Voir également Castleman (tumeur ou maladie de), En anglais : POEMS syndrome. Synonymes : syndrome de Crow-Fukase, syndrome de Takatsuki. Acronyme (sigle prononcé comme un mot ordinaire, sans l’épeler) de :
    P : Polyneuropathie
    O : Organomégalie
    E : Endocrinopathie
    M : Monoclonale
    S : Anomalie cutanée (en anglais : Skinchanges)
    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
    • Hépato splénomégalie : augmentation de volume du foie et de la rate
    • Adénopathie : affection des ganglions
    • Gynécomastie : augmentation des glandes mammaires
    • Impuissance
    • Aménorrhée : absence de règles
    • Hyperpigmentation : augmentation de la coloration cutanée
    • Epaississement de la peau
    Le labo
    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 d’une lignée unique, appelés également clones de cellules plasmocytaires. Les plasmocytes sont issus d’une variété de globules blancs fabriqués dans la moelle osseuse.

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