Results 31 to 40 of about 31,021 (191)

A rare case of solitary brain Langerhans cell histiocytosis with intratumoral hemorrhage in a patient affected by Turner syndrome [PDF]

, 2016
Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of cells with characteristics similar to bone marrow-derived Langerhans cells. The case of a young woman, affected by Turner syndrome and a solitary intraparenchymal LCH
Alafaci, C., Alafaci, E., GRANATA, Francesca, GRASSO, Giovanni, Morabito, Rosa, Salpietro, F.   +5 more
core   +2 more sources

Langerhans cell histiocytosis (histiocytosis x) – in the mandible

Brazilian Dental Science, 2013
This article reports a case of 65 year-old man consultedin a private radiology dental clinic for a panoramicradiography, where was indicated a radiolucent area,extending into the periapical region of the teeth 35 to 43 to the base of the mandible ...
Angela Jordão Camargo, Mayara Cheade, Celso Martinelli, Solange Aparecida Caldeira Monteiro, Christiano de Oliveira Santos, Plauto Christopher Aranha Watanabe   +5 more
doaj   +1 more source

Langerhans´cell histiocytosis [PDF]

, 2014
La histiocitosis de células de Langerhans (HCL), anteriormente conocida como histiocitosis X, es una enfermedad poco frecuente caracterizada por la acumulación y proliferación de histiocitos, eosinófilos y células de Langerhans, con inclusión de gránulos
Casanovas, A., Elena, G., Rosso, Diego
core   +1 more source

Manganese overload as a co-factor of neurological symptoms in a patient with sclerosing cholangitis due to Langerhans cell histiocytosis

Haematologica
Not available.
Jerome Razanamahery, Ahmed Idbaih, Matthias Papo, Fabien Robelin, Jean-Francois Emile, Sylvain Audia, Bernard Bonnotte, Julien Haroche   +7 more
doaj   +1 more source

Hand-Schüller-Christian disease

Indian Journal of Dental Research, 2012
Langerhan cell histiocytosis, formerly known as histiocytosis X, traditionally denotes a group of diseases that stem from proliferative reticuloendothelial disturbances.The etiology and pathogenesis of the disease remain debatable.
Deepak Bhargava, Kalyani Bhargava, Vinay Hazarey, Sindhu Milind Ganvir   +3 more
doaj   +1 more source

Langerhans cell histiocytosis [PDF]

, 1998
The authors present a rare case of Langerhans cell histiocytosis in a 31 year old female patient with vulvar, peri-anal and oral lesions, diabetes insipidus, pulmonary skin and bone infiltrations.
Atallah, Álvaro Nagib, Chauffaille, Maria de Lourdes Lopes Ferrari, Diniz, Cybelle Maria Costa, Enokihara, Silva, Ferreira, Karin Ventura, Hassun, Karine Marques, Kerbauy, José, Martinez, José Antônio Baddini, Michalany, Nylceo, Simões, Milvia Maria, Valério, Rosana M.   +10 more
core   +2 more sources

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

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

Bilateral breast Rosai‐Dorfman disease screen detected by mammography

Clinical Case Reports, 2023
Rosai‐Dorfman disease (RDD) is a proliferative disorder of histiocytes typically found in nodal sites and commonly observed in females. Patients often present with systemic symptoms such as fever, lymphadenopathy, and weight loss.
Christina Sumner, Karma Salem, Luma Abunimer, Abdulwahab Ewaz, Linsheng Zhang, Ashley Monsrud, Nabil Calisi   +6 more
doaj   +1 more source