Results 111 to 120 of about 9,884 (233)

Selective embolization of the internal iliac arteries for the treatment of intractable hemorrhage in children with malignancies [PDF]

, 2011
PurposeAcute internal hemorrhage is an occasionally life-threatening complication in pediatric cancer patients. Many therapeutic approaches have been used to control bleeding with various degrees of success.
Sul Hee Bae, Dong Kyun Han, Hee Jo Baek, Sun Ju Park, Nam Kyu Chang, Hoon Kook, Tai Ju Hwang   +6 more
core   +1 more source

Eosinophilic ulcer of the tongue - Case report. [PDF]

, 2015
Eosinophilic ulcer of the oral mucosa is a rare, self-limiting, chronic and benign lesion of unknown pathogenesis that affects the oral mucosa. We present the case of a 65 year-old Caucasian female with a fivemonth history of a painful ulcer on the ...
Calvieri, Stefano, Didona, B, Didona, D, Donati, M, Paolino, Giovanni   +4 more
core   +2 more sources

Langerhans cell histiocytosis: current concepts in dentistry and case report [PDF]

, 2016
Langerhans cell histiocytosis (LCH), which is a rare granulomatous pediatric disease of unknown etiology, is characterized by the idiopathic proliferation and accumulation of abnormal and clonal Langerhans cells or their ...
Alejo-Gonzalez, Francisco, Garrocho Rangel, Arturo, Pozos Guillén, Amaury de Jesús, Ramos-Gutierrez, Efraín, Ruiz Rodríguez, Socorro   +4 more
core  

A Rare Case of a Systemic Non-Langerhans Histiocytosis Presenting with Diabetes Insipidus and a Tentorial Mass [PDF]

, 2015
Introduction The histiocytoses are a group of clinically diverse diseases distinguished from one another based on the specific immunophenotype of the lesional cells, implying derivation from the same precursor cell.
Barros, MS, Guilherme, Farrell, MD, Christopher J, Kenyon, MD, PhD, Lawrence C, Krupa, BS, Kelly, Krupa, BS, Kristin, Madineni, MD, Ravichandra   +5 more
core   +2 more sources

A RARE CASE OF PULMONARY NON-LANGERHANS CELL HISTIOCYTOSIS [PDF]

Chest, 2020
Victoria Gonzalez, Bernadette Schmidt, Kristen Hughes, Emad Shehada   +3 more
openaire   +1 more source

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

A Rare Case of Erdheim-Chester Disease (Non-Langerhans Cell Histiocytosis) with Concurrent Langerhans Cell Histiocytosis: A Diagnostic and Therapeutic Challenge

Case Reports in Hematology, 2018
Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocyte disorder most commonly characterized by multifocal osteosclerotic lesions of the long bones demonstrating sheets of foamy histiocyte infiltrates on biopsy with or without histiocytic ...
Hamza Hashmi, Drew Murray, John Greenwell, Marwan Shaikh, Soumit Basu, Maxwell Krem   +5 more
doaj   +1 more source

An unusual acute myeloid leukemia associated with hyper IgE: another case of AML‐M5c? [PDF]

, 2001
Haematologica. 2001 Feb;86(2):216-7. An unusual acute myeloid leukemia associated with hyper IgE: another case of AML-M5c? Lima M, Orfão A, Coutinho J, Ferreira G, Freitas I, Silvestre F, Justiça B.
COUTINHO, J., FERREIRA, G., FREITAS, I., JUSTICA, B., LIMA, M., ORFAO, A., SILVESTRE, F   +6 more
core  

Erdheim–Chester Disease Manifesting Without Long Bone Involvement

Respirology Case Reports
Erdheim–Chester Disease (ECD) is an extremely rare, non‐Langerhans cell histiocytosis characterised by the proliferation of foamy histiocytes infiltrating various organs.
Dhiran Sivasubramanian, Karthick Balasubramanian, Mohamed Raghib Hussain Mohamed Kalifa, Sathwik Sanil, Smrti Aravind, Nithish Nanda Palanisamy, Virushnee Senthilkumar   +6 more
doaj   +1 more source

Erdheim–Chester disease: A multisystem non-Langerhans cell histiocytosis with cutaneous involvement

Journal of the Royal College of Physicians of Edinburgh
Erdheim–Chester disease (ECD) is a rare non-Langerhans cell histiocytosis (LCH) marked by systemic involvement and diverse clinical manifestations. We report a 35-year-old man with yellowish-brown periorbital lesions initially diagnosed as xanthelasma, which later recurred.
Neetu Bhari, Ritu Sharma, Sushant Agrawal, Vishal Gaurav   +3 more
openaire   +1 more source