ランゲルハンス細胞肉腫
WordNet
- small room in which a monk or nun lives (同)cubicle
- a device that delivers an electric current as the result of a chemical reaction (同)electric cell
- a room where a prisoner is kept (同)jail cell, prison cell
- (biology) the basic structural and functional unit of all organisms; they may exist as independent units of life (as in monads) or may form colonies or tissues as in higher plants and animals
- any small compartment; "the cells of a honeycomb"
- a small unit serving as part of or as the nucleus of a larger political movement (同)cadre
- a usually malignant tumor arising from connective tissue (bone or muscle etc.); one of the four major types of cancer
PrepTutorEJDIC
- (刑務所の)『独房』;(修道院の)小さい独居室 / (ミツバチの)みつ房,巣穴 / 小さい部屋 / 『細胞』 / 電池 / 花粉室 / (共産党などの)細胞
- 肉腫(にくしゅ)
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/03/30 17:29:46」(JST)
[Wiki en表示]
Langerhans cell sarcoma |
Classification and external resources |
ICD-O: |
M9756/3 |
MeSH |
D054752 |
Langerhans cell sarcoma is a form of malignant histiocytosis. It should not be confused with Langerhans cell histiocytosis, which is cytologically benign.[1] Langerhans cell sarcoma is known to transform into leukemia.[2] It can present in the lung, but such cases are rare.[3]
See also[edit]
References[edit]
- ^ Langerhans Cell Sarcoma at the US National Library of Medicine Medical Subject Headings (MeSH)
- ^ Sumida K, Yoshidomi Y, Koga H, et al. (June 2008). "Leukemic transformation of Langerhans cell sarcoma". Int. J. Hematol. 87 (5): 527–31. doi:10.1007/s12185-008-0063-x. PMID 18360746.
- ^ Jülg BD, Weidner S, Mayr D (March 2006). "Pulmonary manifestation of a Langerhans cell sarcoma: case report and review of the literature". Virchows Arch. 448 (3): 369–74. doi:10.1007/s00428-005-0115-z. PMID 16328350.
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.
English Journal
- Langerhans cell histiocytosis first presenting in the skin in adults: frequent association with a second haematological malignancy.
- Edelbroek JR, Vermeer MH, Jansen PM, Stoof TJ, van der Linden MM, Horváth B, van Baarlen J, Willemze R.SourceDepartments of Dermatology Pathology, Leiden University Medical Center, Leiden, the Netherlands Department of Dermatology, Vrije Universiteit Medical Center, Amsterdam, the Netherlands Department of Dermatology, Academic Medical Center, Amsterdam, the Netherlands Department of Dermatology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands Laboratorium Pathologie Oost-Nederland, Enschede, the Netherlands.
- The British journal of dermatology.Br J Dermatol.2012 Dec;167(6):1287-1294. doi: 10.1111/j.1365-2133.2012.11169.x.
- Background Langerhans cell histiocytosis (LCH) in adults first presenting in the skin is rare. Guidelines for staging, treatment and follow-up are lacking. Objectives To better define staging procedures, treatment results and clinical course in adult patients with LCH first presenting in the s
- PMID 22835048
- Bone and soft tissue tumors of hip and pelvis.
- Bloem JL, Reidsma II.SourceLeiden University Medical Center, Department of Radiology, PO Box 9600, 2300 RC Leiden, The Netherlands. Electronic address: j.l.bloem@lumc.nl.
- European journal of radiology.Eur J Radiol.2012 Dec;81(12):3793-801. doi: 10.1016/j.ejrad.2011.03.101. Epub 2011 Apr 27.
- Objective is to identify epidemiologic and radiologic criteria allowing specific diagnoses of tumors and tumor-like lesions in the hip region and pelvis, and to optimize pre-operative staging. Patients with pelvic tumors are usually older, and their tumors are larger relative to patients with tumors
- PMID 21524868
Japanese Journal
- 皮膚原発のランゲルハンス細胞肉腫--ランゲルハンス細胞組織球症と比較した臨床学的検討
- 骨組織球症--臨床・画像上の特徴と悪性腫瘍との鑑別 (特集 炎症など悪性骨・軟部腫瘍と見まちがう疾患--診断のポイント)
Related Links
- information site for langerhans cell sarcoma. Looking for other cases worldwide. Sarcoma forum , ... L angerhans cell sarcoma is exceedingly rare. It has been reported in both adults and children. Multisystem involvement includes ...
- Langerhans cell sarcoma information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis. ... Langerhans cell sarcoma: Introduction Langerhans cell sarcoma: A ...
★リンクテーブル★
[★]
- 英
- Langerhans cell sarcoma
[★]
細胞
[★]
ランゲルハンス細胞