Results 61 to 70 of about 13,017 (193)

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

, 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, Varsha, D, Siraj, Fouzia, Kaur, M, Kaur, Manveen, Chaudhary, N, Siraj, F, Chaudhary, Neena   +7 more
core   +1 more source

Langerhans Cell Histiocytosis in a Newborn

Journal 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, Chen, Shu-Jen, Yang, Ling-Yu, Tang, Ren-Bin   +3 more
openaire   +2 more sources

EXPRESSION OF ADHESION MOLECULES IN LANGERHANS CELL HISTIOCYTOSIS

, 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, A. STOPPACCIARO, RUCO, Luigi, C. D. Baroni, STOPPACCIARO, ANTONELLA, UCCINI, Stefania, S. UCCINI, D. Vitolo, L.P. RUCO   +8 more
core   +1 more source

Langerhans cell histiocytosis with hemorrhagic uveitis and exudative retinal detachment

, 2018
Ranju Kharel Sitaula,1 Anadi Khatri2 1Uveitis Department, B.P. Koirala Lions Center for Ophthalmic Studies, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal; 2Fellow of Vitreo-Retina Surgery, Lumbini Eye Institute, Siddharthanagar, Nepal ...
Kharel Sitaula R, Khatri A
core  

Langerhans Cell Histiocytosis Diagnosed In An Elderly Patient [histiocitose De Células De Langerhans Diagnosticada Em Um Paciente De Idade Avançada] [PDF]

, 2015
Langerhans cell histiocytosis is a rare disease characterized by proliferation of Langerhans cells. We report a case of Langerhans cell histiocytosis in a 63-year-old patient, who presented an expansile periorbital lesion as the first symptom, in whom ...
de Carvalho K.M., Iyeyasu J.N., Altemani J., Vaz A.C.M., Queiroz L.S., Reis F.   +5 more
core   +1 more source

Langerhans cell histiocytosis: A rare cause of pathological rib fracture

, 2021
Langerhans cell histiocytosis, formerly known as histiocytosis X, represents clonal proliferations of the antigen-presenting dendritic cells, which are normally found in many organs. It is a rare disease which tends to affect children and adolescents. In
Yolcu A., Temiz P., Aydoğdu İ., Tulay C.M.   +3 more
core   +1 more source

Multifocal Langerhans Cell Histiocytosis in an Adult

, 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, Most, Mathew J., Sirkis, Hartley M., Akalin, Ali   +3 more
core  

Langerhans cell histiocytosis presenting as eosinophilic granuloma of the bilateral forearms in an 8-year-old girl: a case report

Journal of Medical Case Reports, 2019
Background Langerhans cell histiocytosis previously known as histiocytosis X is a rare disease of children and young adults with a very broad clinical spectrum. In children, its annual incidence is estimated between 0.2–0.5 per 100,000.
Salahoudine Idrissa, Hind Cherrabi, Boubacar Efared, Kassim Sidibé, Karima Attaraf, Lamiae Chater, Abderahmane Afifi   +6 more
doaj   +1 more source

Langerhans cell histiocytosis: a diagnostic dilemma

, 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, Piper, Kim M, Francis J Hughes, Hughes, Francis J; id_orcid, Ryan, Paul L, Kim M Piper   +5 more
core   +1 more source

Endocrine manifestations in Langerhans cell histiocytosis.

, 2007
Langerhans cell histiocytosis is a rare, multisystem disease that shows a particular predilection for hypothalamo-pituitary axis involvement. Diabetes insipidus is the most frequent permanent consequence of Langerhans cell histiocytosis, developing in ...
Chrousos, GP, Grossman, AB, Kaltsas, GA, Makras, P, Alexandraki, KI   +4 more
core   +2 more sources