Results 101 to 110 of about 4,921,202 (211)

Insights into etiology and management of a case of Langerhans cell histiocytosis manifesting as perianal lesions: a case report

open access: yesJournal of Medical Case Reports
Background Langerhans cell histiocytosis is a rare disorder characterized by abnormal proliferation of Langerhans cells, primarily affecting children and occasionally adults.
Pei Xiao-yue, Tai Zixin, Zhang Wen-jun
doaj   +1 more source

EXPRESSION OF ADHESION MOLECULES IN LANGERHANS CELL HISTIOCYTOSIS

open access: yes, 1993
Expression of adhesion molecules was investigated in six biopsy specimens of Langerhans' cell histiocytosis using immunocytochemistry. Cells with Langerhans' cell histiocytosis morphology were stained for ICAM-1, for the beta-1 integrins alpha-4 (VLA-4 ...
C.D. BARONI   +8 more
core   +1 more source

Langerhans cell histiocytosis: a diagnostic dilemma

open access: yes, 2012
Langerhans cell histiocytosis (LCH) is a rare clonal neoplastic disorder of unknown aetiology which can present with a diverse range of clinical presentations.
Paul L Ryan   +5 more
core   +1 more source

Langerhans Cell Histiocytosis in a Newborn

open access: yesJournal of the Chinese Medical Association, 2009
A full-term female baby was admitted to our hospital at the postnatal age of 37 days with generalized vesiculopapular, crateriform skin lesions. Physical examination revealed a well-nourished baby without fever, hepatosplenomegaly or lymphadenopathy. Laboratory examination was normal except for thrombocytosis (platelet count, 970 x 10(3)/microL).
Yang, Tzu-Ying   +3 more
openaire   +2 more sources

Systemic findings of Langerhans cell histiocytosis in neonatal period

open access: yesRevista de la Facultad de Ciencias de la Salud, 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.
Rosalba Días-Castro   +6 more
doaj   +2 more sources

Langerhans Cell Histiocytosis (Letterer-Siwe disease ) - Report of a case

open access: yes, 2011
Langerhans cell histiocytosis is a rare disorder that occurs when there aretoo many of type of white blood cell called a Langerhans cell. We describe a3-months infant girl who developed wide spread skin lesions since she was 4days of age. . The diagnosis
BS Elagraa   +7 more
core   +1 more source

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

Solitary Langerhans cell histiocytosis of the hard palate: a diagnostic pitfall

open access: yes, 2016
Langerhans cell histiocytosis (LCH) is a relatively rare and unique disease characterized by an abnormal proliferation of immature dendritic cells. It is predominantly seen in children with adults showing less than ten times the incidence compared to ...
Varsha, Dalal   +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

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