Results 21 to 30 of about 5,197,064 (280)

HISTIOCYTOSIS X: CLINICAL OBSERVATIONS

Klinicist, 2014
Two clinical cases of pulmonary Langerhans cell histiocytosis X have been analyzed demonstrating lung and other inner organ pathology, common clinical and X-ray features but different life prognosis.
E. Y. Ponomareva, A. P. Rebrov, E. E. Archangelskaja, A. A. Roshchina, R. N. Steshenko, A. S. Bukia, N. V. Dvornikova, N. N. Moskaleva   +7 more
doaj   +3 more sources

Radiotherapy in langerhans cell histiocytosis : a rare indication in a rare disease [PDF]

, 2013
Introduction: Langerhans Cell Histiocytosis (LCH) represents a rare benign disorder, previously designated as "Histiocytosis X", "Type II Histiocytosis" or "Langerhans Cell Granulomatosis".
Bruns, Frank, Büntzel, Jens, Eich, Hans Theodor, Haverkamp, Uwe, Heyd, Reinhard, Kriz, Jan, Micke, Oliver, Schäfer, Ulrich, Seegenschmiedt, Heinrich   +8 more
core   +3 more sources

Langerhans'-cell histiocytosis (histiocytosis X)--a clonal proliferative disease.

New England Journal of Medicine, 1994
BACKGROUND The lesions of Langerhans'-cell histiocytosis (histiocytosis X), a proliferative histiocytic disorder of unknown cause, contain histiocytes similar in phenotype to dendritic Langerhans' cells.
C. Willman, L. Busque, B. Griffith, B. Favara, K. McClain, M. Duncan, D. Gilliland   +6 more
semanticscholar   +1 more source

Benign TdT-positive cells in pediatric and adult lymph nodes: a potential diagnostic pitfall [PDF]

, 2018
Benign TdT-positive cells have been documented in a variety of non-hematopoietic tissues. Scant data are however available on their presence in non-neoplastic lymph nodes.
AGOSTINELLI, CLAUDIO, Bertuzzi, Clara, BRIGNOLA, STEFANO, Pillon, Marta, Pizzi, Marco, Righi, Simona, Rugge, Massimo, Sabattini, Elena, Semenzato, Gianpietro   +8 more
core   +1 more source

Histiocytosis X: Characteristics, behavior, and treatments as illustrated in a case series

Surgical neurology international, 2011
Background: Langerhans cell histiocytosis (LCH) is a proliferative disorder predominantly found in children. It often presents with pain in calvarium or spine and may cause neuroendocrine symptoms. The gold standard for diagnosing LCH is the detection of
E. Kasper, David H. Aguirre-Padilla, R. Alter, Matthew Anderson   +3 more
semanticscholar   +1 more source

Hand-Schüller-Christian disease

Indian Journal of Dental Research, 2012
Langerhan cell histiocytosis, formerly known as histiocytosis X, traditionally denotes a group of diseases that stem from proliferative reticuloendothelial disturbances.The etiology and pathogenesis of the disease remain debatable.
Deepak Bhargava, Kalyani Bhargava, Vinay Hazarey, Sindhu Milind Ganvir   +3 more
doaj   +1 more source

Erdheim–Chester Disease of the Breast: First Review and First Case of Isolated Severe Gynecomastia

Diagnostics, 2023
(1) Introduction: Erdheim–Chester disease (ECD) is a life-threatening condition and often a diagnostic challenge. It has recently been classified as a hematopoietic tumour, and the cases of ECD reported in the literature has dramatically increased during
Francesco Ruben Giardino, Roberto Cuomo, Mirco Pozzi, Gianluca Marcaccini, Stefano Bacchini, Mohamed Marzouk El Araby, Luca Grimaldi, Giuseppe Nisi   +7 more
doaj   +1 more source

Histiocytosis X and Bronchopulmonary Adenocarcinoma: A Rare Coexistence

Canadian Respiratory Journal, 2002
There exists a rarely observed association between pulmonary histiocytosis X and bronchopulmonary cancer. However, the frequency of bronchopulmonary cancer in these patients is higher than in the general population.
Akýn Kaya, Ýsmail Savas, Elif Pen, Serpil Dizbay Sak, Adem Gungor, Uður Gonullu   +5 more
doaj   +1 more source

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

Cytophagic Histiocytic Panniculitis (CHP) in a Patient with SLE Found after Autopsy: When a Rash Is "Complicated!" [PDF]

, 2019
Introduction: Cytophagic histolytic panniculitis (CHP) is a clinical disorder characterized by nodular panniculitis of the subcutaneous adipose tissue. It was first described in 1980 by Winkelmann.
Abbas, Hafsa, Aslam, Ahsan, Chilimuri, Sridhar, Niazi, Masooma, Saad, Muhammad   +4 more
core   +1 more source