Results 41 to 50 of about 801 (144)

Langerhans Cell Histiocytosis in a Child with Unifocal Mandibular Lesion and Diabetes Insipidus: A Case Report

مجله دانشکده پزشکی اصفهان, 2010
Background: Patients with Langerhans cell histiocytosis are at particularly high risk for central diabetes insipi-dus (CDI) due to hypothalamic-pituitary disease. Langerhans cell histiocytosis (LCH) is a group of idiopathic disorders characterized by the
Zahra Alian, Mahin Hashemipour, Mohammad Hassan Moaddab   +2 more
doaj  

Langerhance Cell Histiocytosis with Primary Cutaneous and Oral Manifestations

مجله دانشکده دندانپزشکی اصفهان, 2007
Introduction: Histiocytosis of lagerhans cell is a spectrum of disorders characterized by proliferation of Histiocyte like cells and includes following: Eosinophilic granuloma, Hand - Schuller Christian disease and Letterer- Siwe disease.
P Ghalyani, A Tavangar, A Aminzadeh
doaj  

Solitary eosinophilic granuloma of the ulna: Diagnosis on fine needle aspiration cytology

Journal of Cytology, 2008
Solitary eosinophilic granuloma is a part of the spectrum of Langerhans cell histiocytoses (LCH) which are rare diseases with varied clinical presentations.
Jain Anshu, Alam Kiran, Maheshwari Veena, Jain Vivek, Khan Roobina   +4 more
doaj  

Perianal Langerhans-Cell Histiocytosis: Review of the Literature

Journal of Coloproctology
Langerhans-cell histiocytosis (LCH) is a rare disorder characterized by the proliferation of Langerhans cells, which originate in the bone marrow. It presents in two main clinical forms: single system LCH (SS-LCH), when the disease involves a single ...
Carlos Augusto Real Martinez, Fabio Guilherme Campos, Fernando Forghieri Silveira, Camila Nardi, Luana Borges Segantine Martins, Naualy Cunha Alencar, Evaldo Pasquini Landi, José Aires Pereira, Danilo Toshio Kanno   +8 more
doaj   +1 more source

Recurrent pulmonary infections as the first presentation of Letterer Siwe disease. [PDF]

Oxf Med Case Reports, 2021
Doya LJ, Dib G, Hassan F.
europepmc   +1 more source

Histiocitosis X: presentación de tres casos

Archivo Médico de Camagüey, 2010
Fundamento: la histiocitosis de células de Langerlhans o también conocido como Histiocitosis X es un grupo de enfermedades entre las cuales se encuentran el Granuloma Eosinofílico, la enfermedad de Hand-Schüller y la enfermedad de Letterer-Siwe, con este
Jorge Santana Álvarez, Juan Miguel Iglesias Solís, Herlán Sánchez Rodríguez, María de los Ángeles Miranda, Sacha Beatriz García Fernández   +4 more
doaj  

Langerhans cell histiocytosis presented as bilateral otitis media and mastoiditis

The Turkish Journal of Pediatrics, 2008
Langerhans cell histiocytosis (LCH) is a rare disease that may affect multiple organs. The etiology of LCH remains unclear to date. It is currently believed that clonal accumulation and proliferation of CD1a-positive Langerhans cells are causative.
Charalampos E Skoulakis, Emmanouil I Drivas, Chariton E Papadakis, Argyro J Bizaki, Pelagia Stavroulaki, Emmanuel S Helidonis   +5 more
doaj  

Multifocal Langerhans' Cell Histiocytosis in an Adult. [PDF]

Iran J Otorhinolaryngol, 2023
Nourizadeh N, Majidi MR, Afzalzadeh MR, Taraz Jamshidi S.   +3 more
europepmc   +1 more source

Mandibular unifocal Langerhans cell histiocytosis in a child - Report of successful management of a rare condition. [PDF]

Int J Surg Case Rep, 2023
Kajal P, Dhingra H, Bhutani N.
europepmc   +1 more source

Diagnosis and treatment of isolated rib Langerhans cell histiocytosis in an adult: A case report. [PDF]

Front Surg, 2023
Guo Y, Huang Q.
europepmc   +1 more source