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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/07/15 05:17:59」(JST)
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- 1. POEMS症候群 poems syndrome
- 2. 免疫誘導性神経障害 immune mediated neuropathies
- 3. 多中心性キャッスルマン病 multicentric castlemans disease
- 4. 多発性骨髄腫の臨床的特徴、検査所見、および診断 clinical features laboratory manifestations and diagnosis of multiple myeloma
- 5. 末梢神経と筋肉に影響を与える腫瘍随伴性症候群 paraneoplastic syndromes affecting peripheral nerve and muscle
Japanese Journal
- 統合失調症における薬物療法の未来をもとめて(5)医療法人社団 東京愛成会高月病院 患者の個別性を重視した精神科医療
- 日本精神科病院協会雑誌 30(8), JN11-273-276, 2011-08
- NAID 40018959360
- N-1 頭皮上脳波・機能的MRIの同時計測によるてんかん性活動の局在 : 皮質脳波所見との比較(神経科学セッション,てんかん制圧:新たなステージに向けて,第41回日本てんかん学会)
- 井内 盛遠,松本 理器,澤本 伸克,花川 隆,浦山 慎一,美馬 達哉,三國 信啓,穴見 公隆,粟屋 智就,加藤 竹雄,高橋 良輔,池田 昭夫,福山 秀直
- てんかん研究 25(3), 243, 2007-09-30
- NAID 110006481033
- 慢性抑うつの女性との精神療法
- 宮崎 伸一
- 精神分析研究 49(1), 68-73, 2005-04-25
- NAID 10016422818
Related Links
- これまでCrow‐Fukase症候群、POEMS症候群、高月病、PEP症候群などの名称で 呼ばれているが､これらはすべて同一のものである。現在本邦においてはCrow‐Fukase 症候群、欧米ではPOEMS症候群と呼ばれることが多い｡ POEMSとは、多発性神経 ...
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★リンクテーブル★
| リンク元 | 「ポエムス症候群」「Takatsuki disease」 |
| 関連記事 | 「病」 |
「ポエムス症候群」
参考
- 1. 単クローン抗体を伴う末梢神経炎 （クロウ・フカセ症候群、POEMS症候群） - 難病情報センター
- 2．[PDF]診断基準など
- 3. 疫学研究としての診断基準
腎障害を伴うPOEMS症候群
- 検索ワード「POEMS syndrome glomerulonephritis」
- Serial renal biopsy findings in a case of POEMS syndrome with recurrent acute renal failure.
- Marked recovery of severe renal lesions in POEMS syndrome with high-dose melphalan therapy supported by autologous blood stem cell transplantation.
- http://www.ncbi.nlm.nih.gov/pubmed/16564945
- Although not included in the acronym, renal lesions also are characteristic of this disease and sometimes require dialysis therapy.
- 腎障害も良く合併するんだって
- POEMS syndrome: definitions and long-term outcome.
- http://www.ncbi.nlm.nih.gov/pubmed/12456500
- The POEMS syndrome (coined to refer to polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes) remains poorly understood. Ambiguity exists over the features necessary to establish the diagnosis, treatment efficacy, and prognosis. We identified 99 patients with POEMS syndrome. Minimal criteria were a sensorimotor peripheral neuropathy and evidence of a monoclonal plasmaproliferative disorder. To distinguish POEMS from neuropathy associated with monoclonal gammopathy of undetermined significance, additional criteria were included: a bone lesion, Castleman disease, organomegaly (or lymphadenopathy), endocrinopathy, edema (peripheral edema, ascites, or effusions), and skin changes.
- Successful stabilisation of nephropathy in a patient with POEMS (polyneuropathy, organomegaly, endocrinopathy, M-band, skin changes) syndrome on treatment with mycophenolate and steroids: a case report
- http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848064/
- Nakamoto et al. [7] reviewed 52 cases of Japanese patients with nephropathy. All patients manifested four or all of the five signs of POEMS. Polyneuropathy was present in all but one patient. A majority of cases had monoclonal protein in blood (either IgA- or IgG-) although 10 demonstrated a polyclonal hypergammaglobulinaemia, but in these, four other signs of POEMS supported the diagnosis.
- Nakamoto et al. [7] -> http://www.ncbi.nlm.nih.gov/pubmed/10528660
- Nakamoto et al. [7] reviewed 52 cases of Japanese patients with nephropathy. All patients manifested four or all of the five signs of POEMS. Polyneuropathy was present in all but one patient. A majority of cases had monoclonal protein in blood (either IgA- or IgG-) although 10 demonstrated a polyclonal hypergammaglobulinaemia, but in these, four other signs of POEMS supported the diagnosis.