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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/03/21 18:19:26」(JST)
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Letterer–Siwe disease |
Classification and external resources |
Specialty |
oncology |
ICD-10 |
C96.0 |
ICD-9-CM |
202.5 |
ICD-O |
9722/3 |
OMIM |
246400 |
DiseasesDB |
5906 |
MeSH |
D006646 |
[edit on Wikidata]
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Letterer–Siwe disease is an old name for Langerhans cell histiocytosis (LCH), from a time when LCH was thought to be several different diseases; Letterer–Siwe disease, Hand-Schuller-Christian disease, Eosinophilic granuloma and Hashimoto-Pritzker disease. Later they were all put together under the name Histiocytosis X. The X was found to be the Langerhans cell, a dendritic white blood cell. LCH is not believed to be genetic, even though there have been a few reports of more than one person affected by LCH within the same family. Still to this day, the cause is unknown, after researchers have worked very hard on trying to figure it out for decades.
The old name, Letterer-Siwe disease, is derived from the names of Erich Letterer and Sture Siwe.
External links
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
- 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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UpToDate Contents
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English Journal
- Building test data from real outbreaks for evaluating detection algorithms.
- Texier G1,2, Jackson ML3, Siwe L4, Meynard JB5, Deparis X5, Chaudet H2.
- PloS one.PLoS One.2017 Sep 1;12(9):e0183992. doi: 10.1371/journal.pone.0183992. eCollection 2017.
- PMID 28863159
- Langerhans Cell Histiocytosis Presenting as a Nodulo-Ulcerative Eyelid Lesion.
- Lo C1, Patel P, Charles NC.
- Ophthalmic plastic and reconstructive surgery.Ophthal Plast Reconstr Surg.2017 May/Jun;33(3S Suppl 1):S51-S52. doi: 10.1097/IOP.0000000000000555.
- PMID 26359698
- Cervical Langerhans cell histiocytosis (histiocytosis X).
- Aw HC1, Li Wai Suen CF1, Longano A2, Mahanta V1, Vallance N1.
- ANZ journal of surgery.ANZ J Surg.2016 Dec;86(12):1056-1057. doi: 10.1111/ans.12794. Epub 2014 Jul 31.
- PMID 25078675
Japanese Journal
- 肺ランゲルハンス細胞組織球症 (特集 稀な呼吸器疾患 : 診断と治療の最前線)
- 症例 Langerhans細胞組織球症(Letterer-Siwe病)の1例
- 顎口腔領域に生じたLangerhans cell histiocytosisの5例
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