Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/01/10 00:32:03」(JST)
[Wiki en表示]
Multicentric reticulohistiocytosis is a multisystem disease beginning usually around the age of 50 years old, and is twice as common in women.[1]:718[2]
See also
- Reticulohistiocytosis
- List of cutaneous conditions
References
- ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
Histiocytosis (D76.0, 277.89)
|
|
WHO-I/Langerhans cell histiocytosis/
X-type histiocytosis |
- Letterer–Siwe disease
- Hand–Schüller–Christian disease
- Eosinophilic granuloma
- Congenital self-healing reticulohistiocytosis
|
|
WHO-II/non-Langerhans cell histiocytosis/
Non-X histiocytosis |
- Juvenile xanthogranuloma
- Hemophagocytic lymphohistiocytosis
- Erdheim-Chester disease
- Niemann-Pick disease
- Sea-blue histiocyte syndrome
- Benign cephalic histiocytosis
- Generalized eruptive histiocytoma
- Xanthoma disseminatum
- Progressive nodular histiocytosis
- Papular xanthoma
- Hereditary progressive mucinous histiocytosis
- Reticulohistiocytosis (Multicentric reticulohistiocytosis, Reticulohistiocytoma)
- Indeterminate cell histiocytosis
|
|
WHO-III/malignant histiocytosis |
- Histiocytic sarcoma
- Langerhans cell sarcoma
- Interdigitating dendritic cell sarcoma
- Follicular dendritic cell sarcoma
|
|
Ungrouped |
|
|
|
cell/phys (coag, heme, immu, gran), csfs
|
rbmg/mogr/tumr/hist, sysi/epon, btst
|
drug (B1/2/3+5+6), btst, trns
|
|
|
|
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. 関節リウマチの診断および鑑別診断 diagnosis and differential diagnosis of rheumatoid arthritis
- 2. 内臓悪性腫瘍の皮膚症状 cutaneous manifestations of internal malignancy
English Journal
- Multicentric reticulohistiocytosis with elevated cytokine serum levels.
- Bennassar A, Mas A, Guilabert A, Julia M, Mascaro-Galy JM, Herrero C.SourceDepartment of Dermatology, Hospital Clinic, Barcelona, Spain.
- The Journal of dermatology.J Dermatol.2011 Sep;38(9):905-10. doi: 10.1111/j.1346-8138.2010.01146.x. Epub 2011 Jun 9.
- Multicentric reticulohistiocytosis (MRH) is an uncommon non-Langerhans cell histiocytosis of unknown etiology. It is a multisystem disorder characterised by a papulonodular skin eruption, mainly in the extensor surfaces, and destructive polyarthritis. Histologically, either cutaneous lesions or the
- PMID 21658110
Japanese Journal
- 今月の症例 インフリキシマブ投与が著効したMulticentric reticulohistiocytosisの1例
Related Links
- 107. 図1 顔面および項部の多発性皮膚病変. 図2 皮膚病変の病理像. 図3 腫脹した 両手指の関節. 図4 DIPを含む各関節の破壊像. Multicentric reticulohistiocytosis 多 中心性細網組織球症. 長嶺 隆二 九州大学整形外科. (2001 年、第 2 回博多リウマチ ...
Related Pictures
★リンクテーブル★
[★]
- 英
- multicentric reticulohistiocytosis
[★]
- 関
- multicenter、multicentre、multicentricity