Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues.

Leukocytosis

An abnormal increase in the number of leukocytes in the blood.


合計: 2

                       


（表示件数）
PMID (PMCID)
27079402
 OTHER Infant, Newborn
[Langerhans cell histiocytosis with atypical and early neonatal debut].
Garcia-Rodriguez E, Bernabeu-Wittel J, Calderon-Lopez G, Pavon-Delgado A.
Arch Argent Pediatr. 2016;114(2):e104-7.
However, the most common blood disorder in Langerhans cell histiocytosis is pancytopenia rather than leukocytosis, so that the diagnosis was delayed.
27079402
 OTHER Infant, Newborn
[Langerhans cell histiocytosis with atypical and early neonatal debut].
Garcia-Rodriguez E, Bernabeu-Wittel J, Calderon-Lopez G, Pavon-Delgado A.
Arch Argent Pediatr. 2016;114(2):e104-7.
We report a case of Langerhans cell histiocytosis with neonatal onset and complex diagnosis: maintained and significant leukocytosis was the predominant data for the first two months of life, so some type of leukemia was considered.