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.

Emphysema



合計: 5

                      


(表示件数)
PMID (PMCID)
29402641
MIXED_SAMPLE Adult
Emphysema, did you say emphysema?
Benzaquen J, Pradelli J, Padovani B, Marquette CH, Leroy S.
Rev Mal Respir. 2018;35(1):83-87.
A 44years old smoker presenting with rapidly evolving emphysema was eventually diagnosed as having Langerhans cell histiocytosis on the basis of a previous chest CT (four years earlier) showing cavitating nodules.
29052290
FEMALE Adult
Pulmonary Langerhans cell histiocytosis "de novo" after lung transplantation.
Gomez-Roman J, Zarrabeitia MT, Santurtun A, Parra JA, Azueta Etxebarria A, Cifrian JM, Freire Salinas J.
Pathol Int. 2017;67(12):632-637.
A pulmonary Langerhans cell histiocytosis is presented in a 40 year-old woman two years after bilateral lung transplantation for emphysema without any signs of Langerhans cells proliferation in the explanted lungs.
25024518
(4094960)
OTHER
Persistent pulmonary interstitial emphysema in a case of Langerhans cell histiocytosis.
Abbey P, Narula MK, Anand R, Chandra J.
Indian J Radiol Imaging. 2014;24(2):121-4.
Persistent pulmonary interstitial emphysema in a case of Langerhans cell histiocytosis.
25024518
(4094960)
OTHER
Persistent pulmonary interstitial emphysema in a case of Langerhans cell histiocytosis.
Abbey P, Narula MK, Anand R, Chandra J.
Indian J Radiol Imaging. 2014;24(2):121-4.
We present the case of a 10-month-old boy with multisystem Langerhans cell histiocytosis showing thin-walled lung cysts along with computed tomography (CT) evidence of persistent pulmonary interstitial emphysema (PPIE), in the absence of pneumothorax or pneumomediastinum.
1356892
OTHER Adult
A case of Langerhans histiocytosis with HIV-like immunodeficiency.
Manna A, Porcellini A, Marelli A, Bianchini E, Pialoux G.
Haematologica. 1992;77(1):73-5.
A case of histiocytosis X (Langerhans type) associated with bullous pulmonary emphysema and acquired immune deficiency, regarding CD4 positive cells, is described.