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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/02/17 00:32:12」(JST)

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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, 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.

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1. 血球貪食リンパ組織球の臨床的特徴および診断 clinical features and diagnosis of hemophagocytic lymphohistiocytosis

English Journal

A case of pagetoid reticulosis treated with fractional laser-assisted photodynamic therapy.

Jung SE1, Kim YC1.
Clinical and experimental dermatology.Clin Exp Dermatol.2015 Jun;40(4):468-70. doi: 10.1111/ced.12528. Epub 2015 Feb 2.
PMID 25645304

Pagetoid reticulosis tumor cells with double expression of TCRγδ and TCRαβ: an off-target phenomenon or genuine expression?

Tomasini D1, Niccoli A1, Crivelli F2.
Journal of cutaneous pathology.J Cutan Pathol.2015 Jun;42(6):427-34. doi: 10.1111/cup.12486. Epub 2015 Apr 27.
Pagetoid reticulosis (PR) is a low-grade primary cutaneous T-cell lymphoma showing localized patches or plaques with an intrapeidermal proliferation of neoplastic T-cells with heterogeneous immunophenotype. We describe a 73-year-old woman with a 8-year history of gluteal lesions of PR, whom large bl
PMID 25754647

Primary cutaneous anaplastic large cell lymphomas with 6p25.3 rearrangement exhibit particular histological features.

Onaindia A1, Montes-Moreno S, Rodríguez-Pinilla SM, Batlle A, González de Villambrosía S, Rodríguez AM, Alegre V, Bermúdez GM, González-Vela C, Piris MA.
Histopathology.Histopathology.2015 May;66(6):846-55. doi: 10.1111/his.12529. Epub 2015 Feb 4.
AIMS: CD30-positive primary cutaneous lymphoproliferative disorders include several entities with differing clinical presentation but overlapping histological features, including lymphomatoid papulosis and primary cutaneous anaplastic large cell lymphoma (C-ALCL). DUSP22-IRF4 locus translocation is
PMID 25131361

Japanese Journal

菌状息肉症との鑑別が困難であった Peripheral T-cell Lymphoma, Not Otherwise Specified の 1 例

西日本皮膚科 77(1), 37-42, 2015
NAID 130005084965

幼少期より長期間にわたって持続した偽リンパ腫

皮膚の科学 13(2), 103-107, 2014
NAID 130004679563

Availability of a Microglia and Macrophage Marker, Iba-1, for Differential Diagnosis of Spontaneous Malignant Reticuloses from Astrocytomas in Rats

Journal of Toxicologic Pathology 26(1), 55-60, 2013
NAID 130003362354

Related Pictures

★リンクテーブル★

リンク元	「細網内皮症」「細網症」「細網組織増殖症」
拡張検索	「histiocytic medullary reticulosis」「lymphoreticulosis benigna」

「細網内皮症」

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

　　[★]

英: reticuloendotheliosis
同: 細網組織増殖症 reticulosis, Retikulose
関: 網内症 reticulosis 細網細胞

[show details]

細網内皮症 : 約 92 件
網内症 : 32 件

「細網症」

　　[★]

英: reticulosis
関: 組織球性髄質性細網症

「細網組織増殖症」

　　[★]

英: reticulosis
関: 細網内皮症

「histiocytic medullary reticulosis」

　　[★] 組織球性髄質細網症

(病名)組織球性髄質細網症

「lymphoreticulosis benigna」

　　[★] ネコひっかき病。良性リンパ細網症

匿名

検索

案内

案内

reticulosis