洞組織球症
WordNet
- commit a sin; violate a law of God or a moral law (同)transgress, trespass
- violent and excited activity; "they began to fight like sin" (同)hell
- estrangement from god (同)sinfulness, wickedness
- an act that is regarded by theologians as a transgression of Gods will (同)sinning
- the 21st letter of the Hebrew alphabet
- any of various air-filled cavities especially in the bones of the skull
- a blood disease characterized by an abnormal multiplication of macrophages
PrepTutorEJDIC
- 〈U〉(宗教・道徳上の)『罪』 / 〈C〉(宗教・道徳上の)『罪の行為』,罪悪 / 〈C〉《特におどけて》違反(過失)の行為 / (宗教・道徳上の)おきてを破る,罪を犯す / (…に)違反(過失)をする,背く《+『against』+『名』》
- sine
- 洞(どう)(骨や組織の中の穴・くぼみなど);静脈洞
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/04/25 23:10:06」(JST)
[Wiki en表示]
Rosai-Dorfman disease |
Micrograph of a lymph node involved by Rosai-Dorfman disease showing emperipolesis. H&E stain.
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Classification and external resources |
ICD-10 |
D76.3 (ILDS D76.360) |
DiseasesDB |
31419 |
Rosai–Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy, is a rare disorder of unknown etiology that is characterized by abundant histiocytes in the lymph nodes throughout the body.[1],[2]
Contents
- 1 Presentation
- 2 History
- 3 See also
- 4 References
Presentation
Lymphadenopathy of the neck is the most common place of histiocyte accumulation, although accumulation outside of lymph nodes may occur, as well. The most common sites of accumulation outside of the lymph nodes are skin, upper respiratory tract, and the sinuses.[3][4] The disease can be also diagnosed in thyroid gland.[5]
The symptoms of this disease vary with the site of accumulation similar to other regional tumors. For instance, accumulation in closed spaces such as the cranium can lead to poor outcomes compared to growth in the dermis of an extremity where surgical excision is possible.
The disease is usually non-progressive and self-limited, but patients can manifest autoimmune hemolytic anemia. It can rarely present with massive hemoptysis. [6] Extra nodal sites such as skin, mucosae, spinal cord and pancreas may be involved.[1]
History
This condition has been named after Ronald F. Dorfman and Juan Rosai. An alternative eponym of this condition is known as Destombes-Rosai-Dorfman syndrome, part of which is named after Pierre-Paul Louis Lucien Destombes.
See also
- List of cutaneous conditions
References
- ^ a b Riyaz, Najeeba; Khader A (2005). "Rosai Dorfman Syndrome". Indian Journal of Dermatology, Venerology and Leprology 71 (5): 342–344. doi:10.4103/0378-6323.16786. PMID 16394460. Retrieved 2 December 2013.
- ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
- ^ Foucar E, Rosai J, Dorfman R (1990). "Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): review of the entity". Semin Diagn Pathol 7 (1): 19–73. PMID 2180012.
- ^ Walid MS, Grigorian AA (2010). "Ethmo-spheno-intracranial Rosai-Dorfman disease". Indian J Cancer 47 (1): 80–81. doi:10.4103/0019-509X.58870. PMID 20071801.
- ^ Lee FY, Jan YJ, Chou G, Wang J, Wang CC. (2007). "Thyroid involvement in Rosai-Dorfman disease.". Thyroid 17 (5): 471–6. doi:10.1089/thy.2006.0192. PMID 17542678.
- ^ Journal, Chest; Lakshmi Varadarajalu, MD; Sunder Thirugnanasambandan, MS; Paul Jude Thangaraj, MS; Ashok Parameswaran, MD; Meghena Mathew*, MBBS (October 2012). "A Rare Presentation of Rosai Dorfman Disease". Chest. 4 142 (meeting abstracts): 998A–998A. doi:10.1378/chest.1389638.
Histiocytosis (D76.0, 277.89)
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WHO-I/Langerhans cell histiocytosis/
X-type histiocytosis |
- Letterer–Siwe disease
- Hand–Schüller–Christian disease
- Eosinophilic granuloma
- Congenital self-healing reticulohistiocytosis
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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
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WHO-III/malignant histiocytosis |
- Histiocytic sarcoma
- Langerhans cell sarcoma
- Interdigitating dendritic cell sarcoma
- Follicular dendritic cell sarcoma
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Ungrouped |
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Index of cells from bone marrow
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Description |
- Immune system
- Cells
- Physiology
- coagulation
- proteins
- granule contents
- colony-stimulating
- heme and porphyrin
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Disease |
- Red blood cell
- Monocyte and granulocyte
- Neoplasms and cancer
- Histiocytosis
- Symptoms and signs
- Blood tests
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Treatment |
- Transfusion
- Drugs
- thrombosis
- bleeding
- other
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UpToDate Contents
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English Journal
- 18F-FDG PET/CT Follow-up of Rosai-Dorfman Disease.
- Albano D1, Bosio G, Bertagna F.
- Clinical nuclear medicine.Clin Nucl Med.2015 Aug;40(8):e420-2. doi: 10.1097/RLU.0000000000000853.
- Rosai-Dorfman disease (RDD) or sinus histiocytosis is a rare histiocytic disorder characterized by massive lymphadenopathy and with extranodal involvement in 25% to 43% of cases. The clinical course of RDD is unpredictable with episodes of exacerbation and remissions that can last many years, and tr
- PMID 26053720
- Rosai-Dorfman disease with atypical intrascrotal involvement.
- Rodríguez Torres C1, Riazuelo Fantova G1, Escartín Martínez I1, Castillo Escudero JJ1, Del Agua Arias C2.
- International journal of urology : official journal of the Japanese Urological Association.Int J Urol.2015 Aug;22(8):794-6. doi: 10.1111/iju.12805. Epub 2015 May 18.
- We describe two new cases of Rosai-Dorfman disease with intrascrotal involvement. Also known as sinus histiocytosis with massive lymphadenopathy, this is a rare entity, usually presenting with massive bilateral cervical lymphadenopathy. It is associated with extranodal involvement in up to 40% of ca
- PMID 25988924
- An unusual presentation of extranodal Rosai-Dorfman disease threatening the airway.
- Swain SK1, Das A2, Sahoo S3, Baisakh MR4, Sahu MC5.
- Auris, nasus, larynx.Auris Nasus Larynx.2015 Jul 15. pii: S0385-8146(15)00165-0. doi: 10.1016/j.anl.2015.06.007. [Epub ahead of print]
- Rosai-Dorfman disease (RDD) is a rare benign systemic histiocytic proliferation, characterized by massive lymph node enlargement and sometimes associated with extranodal involvement. Even though it is considered as a benign disease, fatalities can occur due to its unusually large size and its locati
- PMID 26188562
Japanese Journal
- ランゲルハンス細胞組織球症117例の臨床像と長期予後および画像所見の特徴について
- 塩田 曜子,中澤 温子,宮嵜 治 [他],恒松 由記子,大澤 真木子
- 東京女子医科大学雑誌 83(E1), E178-E193, 2013-01-31
- … 類似した画像所見を呈した良性の病態として Dermoid cyst、Infantile hemangioma、Sinus pericranii、Arachnoid granulation、Fibrous dysplasiaが経験され、発症部位や慢性の経過を示す辺縁の骨硬化の有無などがLCHとの鑑別点となった。 …
- NAID 110009559395
Related Links
- sinus histiocytosis A nonspecific term for an increase in benign histiocytes in peripheral and medullary sinuses of lymph nodes. Aetiology Reaction to tumours or ... Disclaimer All content on this website, including dictionary ...
- Sinus histiocytosis is a rare condition in which a person's lymph nodes accumulate a specific type of cell. Though there is no... ... Sinus histiocytosis with massive lymphadenopathy (SHML) is also called Rosai-Dorfman disease ...
★リンクテーブル★
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- 英
- sinus histiocytosis
- 関
- ロザイ・ドルフマン病