نتایج جستجو برای: langerhans

تعداد نتایج: 11364  

Journal: :iranian journal of blood and cancer 0

langerhans cell histiocytosis (lch) is a rare disorder described as three different entities including eosinophilic granulomaof bone, the hand-schuller-christian syndrome, and letterer-siwe disease. lch is currently classified into singlesystem lch, and multisystem lch. patients with single system lch have an excellent prognosis, and are mostlytreated with local therapy. multisystem lch is subd...

Journal: :BMC Urology 2006
Jun Hagiuda Munehisa Ueno Satoshi Ashimine Isao Kuroda Keisuke Ishizawa Nobuhiro Deguchi

BACKGROUND Langerhans cell histiocytosis affects mainly young children and features an accumulation of CD1a+ dendritic Langerhans cells in the bone, skin, and other organs. A few cases of Langerhans cell histiocytosis on the penis have been reported in the literature. We present a case of Langerhans cell histiocytosis on the penis and review the similar cases in the literature. CASE PRESENTAT...

Journal: :Archives of disease in childhood 1992
R C Yu J F Morris J Pritchard T C Chu

The functional activity of skin cells derived from an infant who died of multisystem Langerhans cell histiocytosis (LCH) was examined. Involved and non-involved skin was obtained at postmortem examination within three hours of death; normal epidermal Langerhans cells and 'LCH cells' were separated by means of dispase digestion. The functional activity of different populations of CD1a positive c...

Journal: :Turkish journal of haematology : official journal of Turkish Society of Haematology 2013
Aylin Orgen Çallı Yelda Morgül İnci Alacacıoğlu Sadi Bener Bahriye Payzin

Langerhans cell sarcoma is a rare, high-grade neoplasm with overtly malignant cytological features and the Langerhans phenotype. Herein, we present a rare case of Langerhans cell sarcoma in a 65-year-old female that presented with a painless enlarging mass in her right axillary region, along with the histopathological features and diagnostic characteristics in the light of literature on Langerh...

Journal: :Infection and immunity 1997
S Flohé T Lang H Moll

Protozoan parasites of the genus Leishmania exist as obligatory intracellular amastigotes and invade macrophages and Langerhans cells, the dendritic cells of the skin. Langerhans cells are much more efficient in presenting Leishmania major antigen to T cells than macrophages are and have the unique ability to retain parasite antigen in immunogenic form for prolonged periods. To analyze the mech...

Journal: :acta medica iranica 0
m. vaziri a. pazooki l. zahedi

pulmonary langerhans cell histiocytosis (plch) is a rare idiopathic disorder that primarily affects young adult cigarette smokers. affected patients often present with cough and dyspnea and about 20% of patients present with or later develop pneumothorax. it is striking that more than 90% of patients are smokers. we report a very unusual case of plch in a 20-year- old male patient with no smoki...

Journal: :The Kurume medical journal 1988
O Mori H Hachisuka H Nomura K Okubo Y Sasai

The effect of etretinate, applied systemically, on epidermal Langerhans cells was studied. The numbers and shapes of Langerhans cells were observed on split epidermis, and the percentage of Langerhans cells in whole epidermal cells was determined with a flow cytometrial system. On an epidermal sheet, the number of Langerhans cells changed biphasically, first the number increased, then decreased...

2015
Saede Atarbashi Moghadam Ali Lotfi Batool Piroozhashemi Sepideh Mokhtari

STATEMENT OF THE PROBLEM Langerhans cell histiocytosis is a rare disease with unknown pathogenesis and is characterized by local or disseminated proliferation of Langerhans cells. There is no previous investigation on prevalence of oral Langerhans cell histiocytosis in Iranian population. PURPOSE The purpose of this study was to assess the relative frequency of oral Langerhans cell histiocyto...

نحوی, اعظم, همتی, سمانه,

Langerhans cell histiocytosis (LCH) is a rare, proliferative disorder which is characterized by proliferation of pathological Langerhans cells within different organs. In 90% of cases the head and neck are affected. In this article, we report a 2.5-year-old boy with LCH who was referred to the pediatric department of Babol Dental School, with a chief complaint of fever, mucosal ulceration, ging...

2014
Yan Chen Ting-Ting Wang Yan Gao Tie-Jun Li

BACKGROUND Calcifying epithelial odontogenic tumour (CEOT) is a rare benign odontogenic tumour, and its Langerhans cell variant is even rarer. Due to the limited number of recorded cases, the biological behaviour and histogenesis of the Langerhans cell variant of CEOT are not yet fully understood. Thus, the correlation between conventional CEOT and the Langerhans cell variant remains to be clar...

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