| 词条 | Non-Langerhans cell histiocytosis |
| 释义 |
| name = Non-Langerhans cell histiocytosis | synonyms = Histiocytosis, Non-Langerhans-Cell [1] | image = | caption = | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Non-Langerhans cell histiocytosis refers to a family of histiocytosis characterized by the absence of Langerhans cells.[2] Many manifest cutaneously.[3] the spectrum of non-langerhans cell histiocytoses include:
References1. ^{{cite web |title=Non-Langerhans-Cell Histiocytosis |url=https://rarediseases.info.nih.gov/diseases/8231/index |website=NIH |publisher=The Genetic and Rare Diseases Information Center (GARD) |accessdate=19 March 2019}} 2. ^{{cite journal |vauthors=Weitzman S, Jaffe R |title=Uncommon histiocytic disorders: the non-Langerhans cell histiocytoses |journal=Pediatr Blood Cancer |volume=45 |issue=3 |pages=256–64 |date=September 2005 |pmid=15547923 |doi=10.1002/pbc.20246}} 3. ^{{cite book|author1=Philip T. Cagle|author2=Timothy C. Allen|author3=Roberto Barrios|title=Color atlas and text of pulmonary pathology|url=https://books.google.com/books?id=QtleIMhv9KAC&pg=PA210|accessdate=14 November 2010|date=1 December 2007|publisher=Lippincott Williams & Wilkins|isbn=978-0-7817-8208-1|pages=210–}} 4. ^{{cite journal |vauthors=Rao RN, Chang CC, Uysal N, Presberg K, Shidham VB, Tomashefski JF |title=Fulminant multisystem non-langerhans cell histiocytic proliferation with hemophagocytosis: a variant form of Erdheim-Chester disease |journal=Arch. Pathol. Lab. Med. |volume=129 |issue=2 |pages=e39–43 |date=February 2005 |pmid=15679446 |doi= 10.1043/1543-2165(2005)129 External links{{Medical resources| DiseasesDB = | ICD10 = D76.3 | ICD9 = | ICDO = | OMIM = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = D015616 | Orphanet = 157987 }}{{Histiocytosis}}{{disease-stub}} 2 : Monocyte- and macrophage-related cutaneous conditions|Histiocytosis |
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