Results 101 to 110 of about 5,248,297 (184)

Langerhans Cell Histiocytosis of the Clavicle in a 13-Year-Old Boy

open access: yesCase Reports in Orthopedics, 2014
Langerhans Cell Histiocytosis (LCH) is a rare neoplasm characterized by abnormal proliferation of histiocytic cells. In this case report, we describe a unique case of a 13-year-old boy who presented to the clinic with an insidious onset of mid-clavicular
Shital N. Parikh   +3 more
doaj   +1 more source

Adult langerhans cell histiocytosis

open access: yes, 2007
Langerhans cell histiocytosis is a group of idiopathic disorders characterized by the abnormal proliferation of specialized bone marrow-derived Langerhans cells. There are one to two cases per million population.
Bahceci, Mithat   +4 more
core   +1 more source

Cerebellar Disease Mimicking Cerebrotendinous Xanthomatosis: Langerhans Cell Histiocytosis

open access: yes, 2017
Item does not contain fulltextBACKGROUND: This report highlights the differential diagnosis of predominant cerebellar white matter abnormalities with dentate nuclei involvement.
Marjo S. van der Knaap   +7 more
core   +1 more source

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

open access: yesPathology 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   +3 more
doaj   +1 more source

Paediatric Langerhans cell histiocytosis with diabetes insipidus: remarkable recovery journey

open access: yesJournal 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   +4 more
doaj   +1 more source

A case of diagnosis and treatment of mediastinal Langerhans cytosis

open access: yesJournal 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   +5 more
doaj   +1 more source

Langerhans’ cell histiocytosis (histiocytosis X): A rare and diverse group of disorder in children [PDF]

open access: yes, 2017
Langerhans cell histiocytosis is a rare disorder of unknown etiology with proliferation of Langerhans’ cells which may infiltrate a single or multiple organs.
Prajapati, Snehal   +2 more
core  

Multifocal Langerhans Cell Histiocytosis in an Adult

open access: yes, 2017
Eosinophilic granuloma (EG) is the most common and benign form of the spectrum of disorders referred to as Langerhans cell histiocytosis (LCH). Langerhans cell histiocytosis is primarily regarded as a pediatric disease, with few adult cases of multifocal
Nielsen, Natalie   +3 more
core  

Unusual Neurological Manifestation of Langerhans Cell Histiocytosis in an Adult

open access: yesEar, Nose & Throat Journal
Langerhans Cell Histiocytosis is a rare disorder characterized by an abnormal proliferation of Langerhans cells in one or multiple organs. It rarely presents with a central vestibular involvement.
Imen Achour MD   +7 more
doaj   +1 more source

Histiocitosis de células de Langerhans con manifestaciones multisistémicas en periodo neonatal [PDF]

open access: yes, 2011
We report an unusual case of mediastinal abcessed mass, with involvement of the lung, thymus and probably bone and hematopoietic system, in a newborn that was diagnosed with Langerhans cell histiocytosis.
Martínez, Gloria   +6 more
core  

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