Results 111 to 120 of about 18,120 (223)

رتيکولوهيستيوسيتوز خود محدود شونده مادرزادی (گزارش 1 مورد با ضايعه منفرد) [PDF]

, 2004
رتيکولوهيستيوسيتوز خود محدود شونده مادرزادی نوعی هيستيوسيتوز سلول لانگرهانس می‌باشد که پاتوفيزيولوژی و عامل آن به خوبی مشخص نشده است. برخی از مولفان مکانيسم‌های ايمنی‌ که موجب افزايش توليد سيتوکين‌ها می‌شوند را در ايجاد آن موثر می‌دانند.
ارجمندی رفسنجانی, خدیجه, مهرآزما, میترا, وثوق, پروانه   +2 more
core  

Erdheim Chester disease – 25 year history with early CNS involvement [PDF]

, 2016
We report a case of Erdheim-Chester disease (ECD) with a 25-year history following initial presentation with diabetes insipidus and brainstem involvement.
Cohen, N, Hall, C A, McCoubrie, Paul, Renowden, S, Rice, Claire, Scolding, Neil   +5 more
core   +2 more sources

Langerhans cell hyperplasia in the tumor stage of mycosis fungoides: a mimic of Langerhans cell histiocytosis [PDF]

, 2011
Mycosis fungoides is a form of cutaneous T-cell lymphoma (CTCL). Malignant CD4+ T cells have been found to adopt the T-regulatory (Treg) cell phenotype and function.
Lin, Tzu-Chun, Wu, Po-Yuan, Lin, Tze-Yi, Yeh, Su-Peng, Chen, Shyh-chang, Lee, Tsong-Liang   +5 more
core   +2 more sources

Intestinal Langerhans cell histiocytosis presenting with symptoms similar to inflammatory bowel disease: a case report

Pathology and Oncology Research
Background:Langerhans cell histiocytosis is a rare disease characterized by the abnormal proliferation of Langerhans cells within a single organ or multiple organs.
Yuqing Liu, Zhenwei Chen, Lu Wang, Baizhou Li   +3 more
doaj   +1 more source

Paediatric Langerhans cell histiocytosis with diabetes insipidus: remarkable recovery journey

Journal of the Pakistan Medical Association
A rare condition known as Langerhans cell histiocytosis (LCH) is characterised by the clonal growth of dendritic cells called Langerhans cells, which play a significant role in the immune system. A diverse range of clinical presentations are probable as
Versha Rani Rai, Zulqarnain Buriro, Roshia Parveen, Mohsina Noor, Heeranand Rathore   +4 more
doaj   +1 more source

A case of diagnosis and treatment of mediastinal Langerhans cytosis

Journal of Cardiothoracic Surgery
Background Langerhans cell histiocytosis (LCH) is a rare disease. It mainly involves abnormal proliferation and aggregation of Langerhans cells, a type of cell of the immune system.Langerhans cytosis is more common in the bone, but it has rarely been ...
Yumeng Niu, Lei Xian, Yi Wang, Yourong Chen, Yifei Lu, Daying Liang   +5 more
doaj   +1 more source

Isolated Langerhans cell histiocytosis of the vulva: a case report and review of the literature [PDF]

, 2018
Isolated Langerhans cell histiocytosis (LCH) of the female genital tract is very rare. A review of the literature revealed that only 15 cases of primary vulvar LCH have previously been published in the English literature.
Beer, Karl, Beneder, Christine, Fleischmann, Achim, ImObersteg, Jeannine, Kuhn, Annette, Mueller, Michael   +5 more
core  

Extra-osseous involvement of Langerhans' cell histiocytosis in children [PDF]

, 2018
The predominant clinical and radiological features of Langerhans' cell histiocytosis (LCH) in children are due to osseous involvement. Extra-osseous disease is far less common, occurring in association with bone disease or in isolation; nearly all ...
Eich, Georg, Gudinchet, François, Hanquinet, Sylviane, Schmidt, Sabine, Tschäppeler, Heinz, Waibel, Peter   +5 more
core  

Langerhans Cell Histiocytosis [PDF]

Ear, Nose & Throat Journal, 2010
Sandra, Camelo-Piragua, Eduardo, Zambrano, Liron, Pantanowitz   +2 more
openaire   +2 more sources

Langerhans Cell Histiocytosis Presenting with Headache and Sellar Mass in an Adult [PDF]

, 2012
Bhattacharya, Rajib K, Newell, Kathy, Pandey, Aradhana, Patel, Vaishali   +3 more
core   +2 more sources