WordNet
- an impairment of health or a condition of abnormal functioning
- caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological
- a painter of letters
PrepTutorEJDIC
- (体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
- 女性の話術芸人 =diseur
- 病気にかかった / 病的な,不健全な(morbid)
- レタリング専門家
- siliconの化学記号
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/05/19 16:27:51」(JST)
[Wiki en表示]
| Letterer–Siwe disease |
| Classification and external resources |
| ICD-10 |
C96.0 |
| ICD-9 |
202.5 |
| ICD-O |
9722/3 |
| OMIM |
246400 |
| DiseasesDB |
5906 |
| MeSH |
D006646 |
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, and even though there have been a few reports of more than one person affected by LCH within the same family, this is not considered to be the answer to the mystery of Langerhans cell histiocytosis. 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
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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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- 1. ランゲルハンス細胞組織球症の臨床症状、病理学的特徴、および診断clinical manifestations pathologic features and diagnosis of langerhans cell histiocytosis [show details]
…the skin. For now, "Langerhans cell histiocytosis" remains the preferred nomenclature; the historical terms histiocytosis-X, Letterer-Siwe disease, Hand-Schuller-Christian disease, and diffuse reticuloendotheliosis …
- 2. ランゲルハンス細胞組織球症の治療treatment of langerhans cell histiocytosis [show details]
…The historical terms histiocytosis-X, Letterer-Siwe disease, Hand-Schuller-Christian disease, and diffuse reticuloendotheliosis should be abandoned. The term "eosinophilic granuloma" is sometimes used to …
- 3. 肺ランゲルハンス細胞組織球症pulmonary langerhans cell histiocytosis [show details]
… Pulmonary Langerhans cell histiocytosis (PLCH), previously called eosinophilic granuloma of the lung, pulmonary Langerhans cell granulomatosis, and pulmonary histiocytosis X, is an uncommon cystic interstitial …
- 4. 小児や青年のランゲルハンス細胞組織球症（好酸球性肉芽腫）骨病変langerhans cell histiocytosis eosinophilic granuloma of bone in children and adolescents [show details]
… 1953, eosinophilic granuloma of bone was classified along with Hand-Schuller-Christian disease (with the classic triad of exophthalmos, diabetes insipidus, and skull lesions) and Letterer-Siwe disease (lymphadenopathy …
- 5. 頭皮の発疹を有する患者へのアプローチapproach to the patient with a scalp disorder [show details]
…involvement is absent. Langerhans cell histiocytosis (LCH) is a rare disorder of histiocytes that can affect multiple organs. Both children and adults can develop LCH. Skin involvement in LCH is most likely to …
English Journal
- Clinical-Radiologic-Pathologic Correlation of Smoking-Related Diffuse Parenchymal Lung Disease.
- Kligerman S1, Franks TJ2, Galvin JR3.
- Radiologic clinics of North America.Radiol Clin North Am.2016 Nov;54(6):1047-1063. doi: 10.1016/j.rcl.2016.05.010. Epub 2016 Aug 22.
- The direct toxicity of cigarette smoke and the body's subsequent response to this lung injury leads to a wide array of pathologic manifestations and disease states that lead to both reversible and irreversible injury to the large airways, small airways, alveolar walls, and alveolar spaces. These inc
- PMID 27719975
- Reconstruction of the C-1 lateral mass with a titanium expandable cage after resection of eosinophilic granuloma in an adult patient.
- Stephens BH1, Wright NM1.
- Journal of neurosurgery. Spine.J Neurosurg Spine.2016 Oct 7:1-5. [Epub ahead of print]
- Spinal involvement occurs frequently in cases of eosinophilic granuloma (EG), but surgical treatment is limited primarily to those with spinal instability. Involvement of the cervical spine is rare, but primarily occurs in the vertebral bodies, and is normally amenable to anterior corpectomy and spi
- PMID 27716017
Japanese Journal
- 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
- 笹岡 邦典,茂木 健司,狩野 証夫 [他],神野 恵治,根岸 明秀
- The KITAKANTO medical journal 58(3), 317-324, 2008-08-01
- 著者らは1992年から2007年の16年間に当科を受診した,顎口腔領域のLangerhans cell histiocytosisの5例(男性2名,女性3名)を経験した.初診時年齢は10ヶ月から65歳であった.顎骨のみに病変が認められたのは3例であったが,顎骨以外には肺と下垂体に認められた症例,体幹部皮膚,側頭骨および後頭骨に認められた症例が各1例認められた.診断に関しては顎骨の画像所見等による臨 …
- NAID 110006881216
Related Links
- Let·ter·er-Si·we disease (lĕt′ər-ər-sī′wē, -sē′və) n. See nonlipid histiocytosis. Letterer-Siwe disease [let´er-er si´we] a hereditary langerhans cell histiocytosis of early childhood, characterized by cutaneous lesions resembling seborrheic ...
- Letterer-Siwe disease synonyms, Letterer-Siwe disease antonyms. Information about Letterer-Siwe disease in the free online English dictionary and encyclopedia. Letterer-Siwe disease - definition of Letterer-Siwe disease by The ...
★リンクテーブル★
[★]
- 英
- Letterer-Siwe disease
- 関
- 組織球症X、ランゲルハンス細胞性組織球症、Letterer-Siwe病、ランゲルハンス細胞肉芽腫症、レットレル・ジーベ病
[★]
ランゲルハンス細胞肉芽腫症
- 関
- histiocytosis X、Langerhans-cell histiocytosis、Langerhans' cell granulomatosis、Letterer-Siwe disease
[★]
- 英
- Letterer-Siwe disease
- 関
- レッテラー・シーベ病、Letterer-Siwe病
[★]
- 疾患：illnessより厳密な概念。「ある臓器に明確な障害が確認され、それによって症状が出ているとはっきり説明できる場合」 (PSY.9)
- 特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9)
- something that is very wrong with people's attitudes, way of life or with society.
- 関
- ail、ailment、disease entity、disorder、ill、illness、malady、sick、sickness
- disease ≠ illness ≠ disorder
[★]
ケイ素
- 関
- silicon