Results 31 to 40 of about 23,888 (239)

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

Isolated Bone Marrow Non-Langerhans Cell Histiocytosis Preceding RUNX1-Mutated Acute Myeloid Leukemia: Case Report and Literature Review.

American Journal of Clinical Pathology, 2019
OBJECTIVES The prevalence of concomitant myeloid neoplasms was recently reported to be unexpectedly high among adults without non-Langerhans cell histiocytosis (non-LCH); however, the coexistence of non-LCH with RUNX1 genetic aberration has not been ...
Areej Al Mugairi, Saeed H. Al Turki, Hind Salama, Khlood Al Ahmadi, K. A. Abuelgasim, M. Damlaj   +5 more
semanticscholar   +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

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

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

The use of topical Rapamycin in successfully treating non-Langerhans cell histiocytosis in a pediatric patient

Journal of Skin and Sexually Transmitted Diseases
Non-Langerhans cell histiocytosis (non-LCH) refers to a collection of medical conditions distinguished by the excessive growth of histiocytes in bodily tissues. It is important to note that these conditions do not meet the established diagnostic criteria
David Pudukadan, Jeevana Mary Jose
semanticscholar   +1 more source

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

Erdheim-Chester disease detected with 99MTC MDP bone SPECT/CT

Journal of the Belgian Society of Radiology, 2012
Erdheim-Chester disease (ECD) is a rare non-Langerhans’ cell histiocytosis. Mild but permanent juxta-articular bone pain in mainly knees and ankles is the most frequent associated symptom.
G Ceulemans, M Keyaerts, L Verbruggen, A Hoorens, C Boulet, D Verdries, M De Maeseneer, B Ilsen, H Everaert   +8 more
doaj   +1 more source