Results 51 to 60 of about 56,324 (305)

HYSTYOCYTOSIS X: VERIFICATION OF DIAGNOSIS

Vestnik Dermatologii i Venerologii, 2018
A clinical case of histiocytosis X, rarely found in the practice of a dermatovenereologist, is described, the pathognomonic clinical symptoms of this dermatosis, including skin lesions, that occur in 50 to 80 % of cases of all forms are displayed.
V. V. Starostenko, L. A. Anisimova, O. A. Sidorenko, E. P. Opruzhenkova   +3 more
doaj   +1 more source

Histiocytosis x: Recurrent isolated mandibular lesion (case report) [PDF]

, 2003
Histiocytosis X usually affects children and adolescents. In our case, a 54-year-old woman was admitted to hospital for evaluating and treatment of an isolated, painless swelling of the left side of the mandible.
Arizanović Marko, Basta-Jovanović Gordana M., Jovanović Milena, Stefanović Predrag   +3 more
core   +1 more source

Clinicopathological characteristics, prognostic factors, and outcomes of elderly patients with lymphoma‐associated hemophagocytic lymphohistiocytosis: A multicenter analysis

Cancer Medicine
Background Lymphoma is the most common secondary cause of hemophagocytic lymphohistiocytosis (HLH) in adults. Lymphoma‐associated HLH (LA‐HLH) in the elderly population is not rare, however, little has been reported regarding clinicopathological ...
Yi Miao, Jing Zhang, Xuzhang Lu, Meng Wu, Bingzong Li, Liang Yu, Miao Sun, Yun Zhuang, Yuqing Miao, Haiwen Ni, Xiaoyan Xie, Jingyan Xu, Yunping Zhang, Min Zhao, Min Xu, Wanchuan Zhuang, Weiying Gu, Guoqiang Lin, Haiying Hua, Jianfeng Zhu, Maozhong Xu, Tao Jia, Ping Liu, Lijia Zhai, Tongtong Zhang, Qiurong Shan, Qiudan Shen, Jun Qian, Chunling Wang, Jianyong Li, Wenyu Shi   +30 more
doaj   +1 more source

A Case of Multisystemic Langerhans Cell Histiocytosis in an Adult

Proceedings of Singapore Healthcare, 2011
Langerhans cell histiocytosis is a rare disease in adults with a myriad of clinical presentations. A case of multisystemic Langerhans cell histiocytosis with involvement of bone, skin, lungs, and the hypothalamic-pituitary-axis is reported.
Chiaw Ling Chng MBBS, MRCP
doaj   +1 more source

Langerhans Cell Histiocytosis In Bone: A Case Report

Turkish Journal of Internal Medicine, 2021
Langerhans cell histiocytosis (LCH) is a rare disease in which histiocytic infiltrations can be seen in bone, skin, lymph nodes, lungs, liver, spleen, bone marrow, central nervous system and endocrine glands.
Özlem Buluz, Orkide Kutlu, Hasan Eruzun, Ayça Zeynep Kutlu, Gizem Meral, Suat Erol Çelik   +5 more
doaj   +1 more source

An unusual case of intertrigo in an adult caused by purely cutaneous Langerhans cell histiocytosis [PDF]

, 2016
We report a case of persistent intertrigo in an adult, eventually diagnosed as cutaneous Langerhans cell histiocytosis (LCH). It is known that LCH has a predilection for intertriginous areas, however purely cutaneous disease as in our case, is uncommon ...
Baldacchino, Godfrey, Betts, Alexandra, Boffa, Michael J., Gatt, Alex   +3 more
core  

Hematopoietic origin of Langerhans cell histiocytosis and Erdheim-Chester disease in adults.

Blood, 2017
Langerhans cell histiocytosis (LCH) and Erdheim-Chester disease (ECD) are rare histiocytic disorders induced by somatic mutation of MAPK pathway genes. BRAFV600E mutation is the most common mutation in both conditions and also occurs in the hematopoietic
Paul Milne, V. Bigley, C. Bacon, A. Néel, N. McGovern, S. Bomken, M. Haniffa, E. Diamond, B. Durham, J. Visser, David Hunt, H. Gunawardena, M. Macheta, K. McClain, C. Allen, O. Abdel-Wahab, M. Collin   +16 more
semanticscholar   +1 more source

Childhood Cancer Survivors in Latin America: Insights Into Health Outcomes and Information Needs

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Childhood cancer survivors (CCSs) face long‐term health challenges, yet the health and specific needs of Latin American survivors remain underexplored. This study aimed to describe the health‐related, psychosocial late effects, and information needs among CCSs in the region. Methods This mixed‐method study combined quantitative data
Ana Carolina Izurieta‐Pacheco, David H. Noyd, Julia Challinor, Nuria Rossell, Maria Fernanda Olarte‐Sierra, Daniel Bastardo Blanco, Marcela Zubieta, Nicholas B. George, Sara Perez‐Jaume, Anna Felip‐Badia, Viviana Trigoso, Patricia Loggetto, Valeska Gonzalez, Carlos Frias, Sinders Rincon, Roberta Ortiz, Soad Fuentes‐Alabi de Aparicio, Liliana Vásquez Ponce   +17 more
wiley   +1 more source

Impact of BRAFV600E mutation on aggressiveness and outcomes in adult clonal histiocytosis

Frontiers in Immunology, 2023
Histiocytoses encompass a wide spectrum of diseases, all characterized by tissue infiltration by CD68+ histiocytes. Most adult histiocytoses are considered clonal diseases because they highlight recurrent somatic mutations in the MAP-kinase pathway gene,
Jerome Razanamahery, Amelie Godot, Vanessa Leguy-Seguin, M. Samson, Sylvain Audia, Bernard Bonnotte   +5 more
doaj   +1 more source

Differential Diagnoses of Systemic Mastocytosis in Routinely Processed Bone Marrow Biopsy Specimens: A Review [PDF]

, 2010
Diagnosis of systemic mastocytosis (SM) is mainly based on the morphological demonstration of compact mast cell infiltrates in various tissue sites. In almost all patients such infiltrates are detected in the bone marrow.
Horny, H. -P., Sotlar, K., Valent, P.
core   +1 more source