Results 21 to 30 of about 14,204,460 (231)

High prevalence of myeloid neoplasms in adults with non–Langerhans cell histiocytosis [PDF]

Blood, 2017
Key Points Some 10.1% of adults with non–Langerhans cell histiocytosis have a concomitant myeloid neoplasm with each often harboring distinct mutations. The presence of distinct kinase mutations in histiocytosis and myeloid neoplasms resulted in discordant responses to targeted therapy.
Papo, Matthias, Diamond, Eli, Cohen-Aubart, Fleur, Emile, Jean-François, Roos-Weil, Damien, Gupta, Nishant, Durham, Benjamin, Ozkaya, Neval, Dogan, Ahmet, Ulaner, Gary, Rampal, Raajit, Kahn, Jean-Emmanuel, Sené, Thomas, Charlotte, Frédéric, Hervier, Baptiste, Besnard, Caroline, Bernard, Olivier, Settegrana, Catherine, Droin, Nathalie, Hélias-Rodzewicz, Zofia, Amoura, Zahir, Abdel-Wahab, Omar, Haroche, Julien   +22 more
openaire   +3 more sources

Congenital Self-Healing Langerhans Cell Histiocytosis: A Rare Presentation of Blueberry Muffin Baby “Spectrum”

Dermatopathology, 2019
A case of congenital self-healing Langerhans cell histiocytosis (CSHLCH), also known as Hashimoto-Pritzker disease, is reported. The newborn presented as blueberry muffin baby at birth, showing numerous non-blanching blue-purplish and dark-red papular ...
Katharina Hansel, Marta Tramontana, Stefania Troiani, Diletta de Benedictis, Leonardo Bianchi, Rosa Cucchia, Stefano Simonetti, Luca Stingeni   +7 more
doaj   +1 more source

Indeterminate Cell Histiocytosis: A Case Report

Kaohsiung Journal of Medical Sciences, 2004
Indeterminate cell histiocytosis is a rare neoplasm composed of cells with mixed characteristics of Langerhans cells and non-Langerhans cells. An otherwise healthy, 36-year-old woman presented with asymptomatic generalized papules and nodules that had ...
Chun-Hua Wang, Gwo-Shing Chen
doaj   +1 more source

ADULT ONSET XANTHOGRANULOMA – CASE REPORT AND REVIEW OF LITERATURE [PDF]

Romanian Medical Journal, 2019
Juvenile xanthogranuloma represents the most common form of non-Langerhans cell histiocytosis. It is tipically a childhood disorder, over 80% of cases developing in the first year of life.
Liliana Gabriela Popa, Mara Madalina Mihai, Olguta Anca Orzan, Cristina Beiu, Tiberiu Tebeica, Calin Giurcaneanu   +5 more
doaj   +1 more source

Unusual facial lesions in H syndrome

Clinical Case Reports, 2022
H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions.
Mariem Rekik, Emna Bahloul, Mohamed Ben Rejeb, Khadija Sellami, Slim Charfi, Hamza Chouk, Tahya Boudaouara, Hamida Turki   +7 more
doaj   +1 more source

Clinical experience in an infant with Langerhans cell histiocytosis

Universidad Médica Pinareña, 2021
Introduction: Langerhans cell histiocytosis (LCH) or Histiocytosis X is a benign proliferative disease affecting dendritic cells. It presents a wide clinical spectrum, from isolated eosinophilic bone granuloma to multisystem involvement with multiple ...
Yamilka Pita Barrios, Surelys Peralta Santiesteban, César Adrián Blanco-Gómez   +2 more
doaj  

Indeterminate cell histocytosis with naïve cells

Rare Tumors, 2013
Histiocytoses are a heterogeneous group of disorders characterized by proliferation and accumulation of cells of mononuclearmacrophage system and dendritic cells.
Sheren F Younes, Mona A Kandil, Rehab M Samaka, Ola A Bakry   +3 more
doaj   +1 more source

Cutaneous Rosai-Dorfman Disease - A Rare Non-Langerhans Cell Histiocytosis

JK Science
Cutaneous Rosai-Dorfman disease is classified as non-Langerhans cell histiocytosis. It is a benign lymphoproliferative disorder involving only skin and subcutaneous tissue, which is rare and not well documented.
Afthab Jameela Wahab, S. Athilakshmi, Nivvedhetha S   +2 more
doaj   +1 more source

Uncommon variants of Non-Langerhans Cell Histiocytosis [PDF]

, 2019
Background: Histiocytosis are rare disorders of the mononuclear phagocyte system, characterized by a derangement in differentiation, proliferation or function of monocytes and dendritic cells.
Chiara Moltrasio, Arturo Bonometti, Emanuela Passoni, Emanuela De Juli, Gianluca Nazzaro, Marco Paulli, Silvia Alberti-Violetti, Filippo Bagnoli, Emilio Berti, Jessica Gliozzo   +9 more
core   +2 more sources

Isolated Adult Langerhans' Cell Histiocytosis in Cervical Lymph Nodes: Should It Be Treated?

, 2011
Objective: We report an extremely rare case of Langerhans' cell histiocytosis involving isolated cervical lymph nodes, and we discuss the diagnosis and treatment of this infrequent disease.
羅武嘉;鄭博文, Lo, W-C; Chen, C-C; Tsai, C-C; Cheng, P-W   +1 more
core   +1 more source