| 词条 | X-type histiocytosis |
| 释义 |
| name = | synonym = | image = | image_size = | alt = | caption = | pronounce = | specialty = dermatology | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} X-type histiocytoses are a clinically well-defined group of cutaneous syndromes characterized by infiltrates of Langerhans cells, as opposed to Non-X histiocytosis in which the infiltrates contain monocytes/macrophages.[1]{{rp|720}} Conditions included in this group are:[1]{{rp|720–4}}
See also
References1. ^1 {{cite book |author1=James, William D. |author2=Berger, Timothy G. |title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |location= |year=2006 |pages= |isbn=0-7216-2921-0 |oclc= |doi= |accessdate=|display-authors=etal}} {{Histiocytosis}}{{Cutaneous-condition-stub}} 2 : Monocyte- and macrophage-related cutaneous conditions|Histiocytosis |
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