Preferred Name

Langerhans Cell Histiocytosis

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3107

ALT_DEFINITION

A group of rare disorders in which too many Langerhans cells (a type of white blood cell) grow in certain tissues and organs including the bones, skin, and lungs, and damage them. Langerhans cell histiocytosis may also affect the pituitary gland (which makes hormones that control other glands and many body functions, especially growth). Langerhans cell histiocytosis is most common in children and young adults.

Tissue infiltration by Langerhans cells (histiocytes). When infiltration involves the pituitary stalk or gland, presentation includes diabetes insipidus, which is sometimes accompanied by other pituitary dysfunction.

code

C3107

Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C126659

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C168661

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C168655

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C177537

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C168657

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C103078

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C157711

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118168

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C102905

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118467

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C168662

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C168656

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C168658

Contributing_Source

NICHD

CTEP

CTRP

GDC

Cellosaurus

DEFINITION

A neoplastic proliferation of Langerhans cells which contain Birbeck granules by ultrastructural examination. Three major overlapping syndromes are recognized: eosinophilic granuloma, Letterer-Siwe disease, and Hand-Schuller-Christian disease. The clinical course is generally related to the number of organs affected at presentation. (WHO, 2001)

Display_Name

Langerhans Cell Histiocytosis

FULL_SYN

Langerhans Cell Granulomatosis

Langerhans Cell Histiocytosis

Langerhans cell histiocytosis

Histiocytosis X

Langerhans cell histiocytosis, NOS

Langerhans cell granulomatosis

LCH

ICD-O-3_Code

9751/1

9751/3

9753/1

9754/3

9752/1

Is_Value_For_GDC_Property

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C176985

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C177621

label

Langerhans Cell Histiocytosis

Legacy Concept Name

Langerhans_Cell_Histiocytosis

Maps_To

9751/1

9751/3

Langerhans cell histiocytosis, NOS

Langerhans cell granulomatosis

Histiocytosis X, NOS

Neoplastic_Status

Undetermined

Preferred_Name

Langerhans Cell Histiocytosis

prefixIRI

Thesaurus:C3107

prefLabel

Langerhans Cell Histiocytosis

Semantic_Type

Neoplastic Process

UMLS_CUI

C0019621

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C150692

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