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.

Eosinophilia

Increased count of eosinophils in the blood.


合計: 3

                       


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PMID (PMCID)
12604889
 MIXED_SAMPLE Adult
Eosinophilic pancreatitis and increased eosinophils in the pancreas.
Abraham SC, Leach S, Yeo CJ, Cameron JL, Murakata LA, Boitnott JK, Albores-Saavedra J, Hruban RH.
Am J Surg Pathol. 2003;27(3):334-42.
Eosinophilic pancreatitis is one rare etiology of pancreatic eosinophilia, but other described causes of eosinophilic infiltrates have also included pancreatic allograft rejection, pancreatic pseudocyst, lymphoplasmacytic sclerosing pancreatitis (LPSP), inflammatory myofibroblastic tumor, and histiocytosis X.
3384662
 MIXED_SAMPLE Adult
[Facial granuloma. On the clinic-histologic extent of variations of finding in 5 patients].
Buchner SA, Koch B, Itin P, Schulin C, Rufli T.
Hautarzt. 1988;39(4):217-22.
Differential diagnosis includes sarcoidosis, discoid lupus erythematosus, erythema elevatum et diutinum, angiolymphoid hyperplasia with eosinophilia and histiocytosis X.
309577
 MIXED_SAMPLE
[Eosinophilic granuloma of the conjunctiva].
Knobel H, von Domarus D.
Ophthalmologica. 1978;177(1):47-52.
The differential diagnosis of atypical histiocytosis X, eosinophilic leukaemoid and eosinophilia persistens is discussed.