Results 91 to 100 of about 9,012 (189)

Erdheim Chester Disease treated successfully with cladribine [PDF]

, 2016
A 61-year-old previously healthy male with a history of progressive fatigue, lower extremity edema, and dyspnea for 4 months was hospitalized with pericardial and pleural effusions (Figure 1A, B).
Azadeh, Natalya, Fonseca, Rafael, Gotway, Michael B., Mookadam, Farouk, Tazelaar, Henry D.   +4 more
core   +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

Langerhans Cells as Macrophages in Skin and Lymhphoid Organs [PDF]

, 1980
Properties of epidermal Langerhans cell were compared with those of a number of other dendritic cells in lymphoid organs and of mononuclear phagocytes. Among the dendritic “reticulum” cells included were indetenninate dendritic cells from the epidermis ...
Axelsson, Balfour, Basset, Beachey, Bell, Berken, Birbeck, Bleehan, Breathnach, Breathnach, Breathnach, Breathnach, Brun, Brune, Campo-Aasen, Carswell, Chen, Chen, Cohen, Cohn, Cormane, Cowing, Cruickshank, Dailey, Dailey, Davies, Dukor, Eikelenboom, Eikelenboom, Ellner, Falck, Fedorko, Fedorko, Forsum, Frelinger, Fritsch, Furth van, Furth van, G. Jeanette Thorbecke, Gery, Giacometti, Giacometti, Gianotti, Gigli, Goldyne, Greaves, Hashimoto, Herd, Hirsch, Hoefsmit, Hoefsmit, Hoffmann-Fezer, Humphrey, Hunter, Hunter, Häyry, Inga Silberberg-Sinakin, Jarrett, Johnson, Jouvenaz, Juhlin, Kamperdijk, Kamperdijk, Katz, Kelly, Kischer, Klareskog, Kondo, Kumakiri, Kurland, Lang, Lay, Lerman, Lessard, Lieberman, Lipsky, Lupulescu, Masutani, Mecalf, Miller, Mishima, Muller-Hermelink, Nathan, Nathan, Nettesheim, Nettesheim, Nezelof, Nix, Nordin, Norquist, Nossal, Nossal, Olah, Padilla, Papamichael, Pathak, Pernis, Ponzio, Rabinovitch, Rausch, Reams, Reyes, Rodd van, Rode, Rosenstreich, Rouse, Rowden, Rowden, Rowden, Rowden, Sagebiel, Sanel, Schellander, Schwartz, Schwartz, Schwartz, Schwartz, Schweizer, Shelley, Shelley, Shwartz, Silberberg, Silberberg, Silberberg, Silberberg, Silberberg, Silberberg-Sinakin, Silberberg-Sinakin, Silberberg-Sinakin, Silberberg-Sinakin, Silvers, Snell, Stecher, Steinman, Steinman, Steinman, Steinman, Steinman, Steinman, Steinman, Stingl, Stingl, Stingl, Stingl, Streilein, Szakal, Tamaki, Tarnowski, Thomas, Thomas J. Flotte, Thorbecke, Tweel van den, Umetsu, Unanue, Unanue, van Dorp, van Ewijk, van Furth, van Haelst, Veerman, Veldman, Veldmann, Vemon, Wachsmuth, Williams, Wolff, Wolff, Wolff, Wolff, Wolff, Zelickson, Zurier   +171 more
core   +1 more source

Juvenile xanthogranuloma of the cerebellopontine angle: A case report and review of the literature

Otolaryngology Case Reports, 2019
Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis, most often presenting with skin lesions of the head, neck, and upper trunk. Intracranial presentations have been previously described, however, due to its rarity, treatment algorithms
Sarah M. Tittman, Ashley M. Nassiri, Nauman F. Manzoor, Robert J. Yawn, Bret C. Mobley, John C. Wellons, III, Alejandro Rivas   +6 more
doaj  

An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]

, 2016
Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Bencivinni, F., Brunori, G., Giannitrapani, L., Seidita, A., Serruto, A., Soresi, M.   +5 more
core   +2 more sources

Langerhans cell histiocytosis of the thyroid mimicking thyroiditis in a boy: a case report and literature review

BMC Pediatrics
Background Langerhans cell histiocytosis affecting the thyroid commonly presents with nonspecific clinical and radiological manifestations. Thyroid Langerhans cell histiocytosis is typically characterized by non-enhancing hypodense lesions with an ...
Yu Fan Cheng, Ching Che Wang, Pei Shan Tsai, Dao Chen Lin, Wen Hui Huang   +4 more
doaj   +1 more source

Airway involvement in interstitial lung disease [PDF]

, 2006
PURPOSE OF REVIEW: After briefly discussing several ways to approach airway involvement in interstitial lung diseases - by diagnostic methodologies used to assess it, considering different topographical involvement, related to its presence in the diffuse
Robalo-Cordeiro, C
core   +1 more source

Gastrointestinal Langerhans cell histiocytosis responding to cladribine and imatinib mesylate [PDF]

, 2010
Gastrointestinal involvement in Langerhans cells histiocytosis (LCH) is extremely rare. An optimal treatment regimen is not defined yet and its prognosis is relatively poor.
Agreda Vásquez, Gladys Patricia, Lome Maldonado, Carmen, Oviedo, Edgar, Popoca Barriga, Ulises, Sánchez Guerrero, Sergio Arturo   +4 more
core  

Radiological conference. Langerhans' cell histiocytosis [PDF]

, 1997
published_or_final_versio
Chin, ACW, Peh, WCG
core  

Altano-axial subluxation with torticollis secondary to Langerhans cell histocytosis

Interdisciplinary Neurosurgery, 2017
Langerhans Cell Histiocytosis is a rare disease featuring aberrant proliferation of dendritic cells that can infiltrate the bony skeleton. The authors report a case of six-year-old female presenting with torticollis. She was found to have extensive lytic
Joshua Y. Chua, MD, Ji Min Ling, FRCS, Derrick W.Q. Lian, FRCPath, Mei Yoke Chan, FRCP, David C.Y. Low, FRCS, Sharon Y.Y. Low, PhD, FRCS   +5 more
doaj