Difference between revisions of "Langerhans cell histiocytosis"
Jump to navigation
Jump to search
(+cat.) |
m (→General: w) |
||
Line 2: | Line 2: | ||
==General== | ==General== | ||
*Looks like | *Looks like [[pulmonary Langerhans cell histiocytosis]] - see ''[[Medical_lung_diseases#Pulmonary_Langerhans_cell_histiocytosis|medical lung diseases]]''. | ||
==Microscopic== | ==Microscopic== |
Revision as of 01:20, 20 November 2011
Langerhans cell histiocytosis, abbreviated LCH, is a rare genetic disorder of tissue macrophages. It broadly fits into the category of histiocytoses.
General
- Looks like pulmonary Langerhans cell histiocytosis - see medical lung diseases.
Microscopic
Features:
- Langerhans cells histiocytes - key feature.
- Clusters of cells (histiocytes) with a reniform (kidney-shaped) nucleus and abundant foamy cytoplasm.
- Nucleus may look like a "coffee bean", i.e. have nuclear grooves (similar to those in papillary thyroid carcinoma) -- appearance dependent on the rotation of the nucleus.[1]
- Chromatin pattern: fine granular, light gray.
- Clusters of cells (histiocytes) with a reniform (kidney-shaped) nucleus and abundant foamy cytoplasm.
- +/-Eosinophils - often prominent.
Images:
DDx:
- Kimura disease - eosinophilia.
- See lymph node pathology.
IHC
- CD1a +ve.
- S100 +ve.
Electron microscopy
See also
References
- ↑ BN. 15 March 2011.