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Therapie des Xanthoma disseminatum – eine systematische Literaturrecherche

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 9, Page 1061-1070, September 2025.
Zusammenfassung Das Xanthoma disseminatum ist eine seltene Erkrankung aus dem Spektrum der Nicht‐Langerhans‐Zell‐Histiozytosen, welche in drei Gruppen eingeteilt werden kann und teilweise mit einer Systembeteiligung einhergeht. Da die Erkrankung selten ist, fehlen standardisierte Therapierichtlinien, wodurch die Behandlung im klinischen Alltag ...
Inga Hansen‐Abeck, Mina Hillemans, Finn Abeck, Stefan W. Schneider, Nina Booken   +4 more
wiley   +1 more source

Histiocytosis X: Langerhans’ Cell Histiocytosis

Hematology/Oncology Clinics of North America, 1987
Histiocytosis X is a complex and poorly understood entity. Nevertheless, it would appear as if certain themes are found recurrently throughout the literature dealing with this disease and a review of them serves as a useful summary. 1. Problems with Nomenclature.
openaire   +3 more sources

Multisystem Langerhans' cell histiocytosis (Hand-Schüller-Christian disease) in an adult: a case report and review of the literature [PDF]

, 2018
Langerhans' cell histiocytosis (LCH) is a rare and enigmatic clonal disorder that affects mainly children. It is characterized by single or multiple granulomatous mass lesions composed of cells with the Langerhans' cell phenotype.
Jaques, B., Lombardi, T., Monnier, P., Scolozzi, P.   +3 more
core  

Macrophage Activation Syndrome as Onset of Systemic Lupus Erythematosus: A Case Report and a Review of the Literature [PDF]

, 2015
Macrophage activation syndrome (MAS) is a potentially fatal condition. It is a rare complication of several autoimmune disorders, including systemic lupus erythematosus (SLE) and systemic juvenile idiopathic arthritis (sJIA).
Didona, Dario, Feola, Aldo, Granata, Guido, Granata, Massimo, Stifano, Giuseppina   +4 more
core   +4 more sources

Pulmonary Histiocytosis X

Annals of Saudi Medicine, 1998
g twice a day.In November 1994 she was re-admitted to a secondhospital with a right-sided pneumothorax. In addition tothe pneumothorax, the chest x-ray showed diffuseinterstitial infiltration of both lungs, with normal lungvolumes. Computed tomography (CT) of the chest showeddiffuse interstitial disease, with multiple thin and thick-walled cysts of ...
Abdullah Al-Shimemeri, Hamdan Al-Jahdali, Mohamed S. Al-Moamary, Hanaa Bamefleh   +3 more
openaire   +3 more sources

The clinicopathological characteristics and differential diagnosis of histiocytosis

Chinese Journal of Contemporary Neurology and Neurosurgery, 2015
The histiocytosis is divided into Langerhans' cell histiocytosis (histiocytosis X) and non-Langerhans' cell histiocytosis (NLCH). The former mainly occurs in lymphatic hematopoietic tissue and often involves central nervous system (CNS).
Shi-zhu YU
doaj  

A CASE OF HISTIOCYTOSIS IN THE PATIENT SUSPECTED TO HAVE PULMONARY TUBERCULOSIS

Туберкулез и болезни лёгких, 2019
The article describes the clinical case of Langerhans cell histiocytosis with lesions in lungs and flat bones in a 40-year-old smoker. During 4 years, all stages of the disease were followed.
M. A. Karnaushkina, D. V. Burenchev, A. D. Strutynskaya   +2 more
doaj   +1 more source

Somatic mutations in solid tumors: a spectrum at the service of diagnostic armamentarium or an indecipherable puzzle? The morphological eyes looking for BRAF and somatic molecular detections on cyto-histological samples [PDF]

, 2016
This review article deals with the analysis and the detection of the morphological features associated with somatic mutations, mostly BRAF(V600E) mutation, on both cytological and histological samples of carcinomas.
Abildgaard, Al-Maghrabi, Amoura, Auclair, Baker, Baltazar, Baltazar, Baltazar, Baltazar, Baltazar, Baltazar, Basolo, Basolo, Bedossa, Biegel, Birner, Birner, Catovsky, Cerutti, Chen, Chiarle, Cho, Choi, Christensen, Ciarrocchi, Clegg, Cornillon, Cox, Cramer, Czyz, Dexter, Diebold, Draetta, Fadda, Fadda, Falini, Fend, Fisher, Flaherty, Frankel, Ghossein, Gilliland, Godeau, Hahn, Hoffmann, Hwang, Iseki, James, Jo, Johnston, Kebebew, Kitamura, Kumar, Kurman, Kurman, Lam, Lee, Leite, Marais, Marais, Marais, Maruyama, McCarthy, Mechtersheimer, Miccoli, Mino-Kenudson, Miziorko, Naidu, Nikiforov, Nikiforov, Nikiforov, Nikiforov, Nikiforova, Odze, Pai, Park do, Pelizzo, Picarsic, Pignata, Prasad, Pujade-Lauraine, Raab, Rollins, Rossi, Saki, Santagata, Santoro, Schmitt, Schmitt, Schmitt, Sciot, Sepulveda, Sharrock, Shih, Shoenfeld, Shong, Sobrinho-Simões, Stokloza, Suh, Tagawa, Tóth, Vandenberghe, Vandenberghe, Vitale, Ward, Waxman, Weitzman, Westerman, White, White, Widlund, Xing, Zenz   +112 more
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A Rare Cause of Recurrent Left Knee Pain in an Adolescent Male: A Case Report of Distal Femoral Brodie's Abscess

Clinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT Brodie's abscess, a subacute form of osteomyelitis, is characterized by localized symptoms and can be challenging to diagnose due to its nonspecific clinical presentation. We report a rare case of distal femoral Brodie's abscess in a healthy child, emphasizing the diagnostic intricacies and management.
Adeel Ahmed Siddiqui, Muhammad Waqas Khan, Sajjad Ahmed, Taimoor Ali, Asif Ali, Hussain Haider Shah, Tirth Dave   +6 more
wiley   +1 more source

Letterer–Siwe Disease (LSD): A Case Report

Sudan Journal of Medical Sciences, 2018
Background: Letterer–Siwe Disease (LSD) is one of the variants of Langerhans cell histiocytosis (LCH), which is considered as a rare disease that affects many systems in the body; it is characterized by monoclonal migration and proliferation of specific ...
Suad H. H., Mona Mohamed Elamin, Gad Allah Modawe, Khalid Abd Elmohsin Awad Elseed   +3 more
doaj   +1 more source