Results 11 to 20 of about 9,012 (189)

Successful Treatment of Non-Langerhans Cell Histiocytosis With Topical Rapamycin in Two Pediatric Cases

Clinical, Cosmetic and Investigational Dermatology, 2022
Raden Mohamad Rendy Ariezal Effendi, Trustia Rizqandaru, Renata Yuliasari, Srie Prihianti Gondokaryono, Inne Arline Diana, Reiva Farah Dwiyana Department of Dermatology and Venereology, Faculty of Medicine, Universitas Padjadjaran - Dr.
Effendi RMRA, Rizqandaru T, Yuliasari R, Gondokaryono SP, Diana IA, Dwiyana RF   +5 more
doaj   +3 more sources

Intra-arterial Melphalan for Neurologic Non-Langerhans Cell Histiocytosis [PDF]

Neurology, 2021
Histiocytic neoplasms are rare hematologic disorders characterized by pathologic infiltration of activated histiocytes in affected tissues. The treatment of histiocytic neoplasms, including Langerhans cell histiocytosis (LCH) and non-LCH, has advanced in recent years owing to targeted kinase inhibitors (BRAF and MEK) as patients with somatic mutations ...
Jasmine H. Francis, Y. Pierre Gobin, Ruham Alshiekh Nasany, Jared Knopman, Gary A. Ulaner, Katherine S. Panageas, Vaios Hatzoglou, Kim Salvaggio, David H. Abramson, Athos Patsalides, Eli L. Diamond   +10 more
openaire   +3 more sources

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

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   +4 more sources

PAPULAR HISTIOCYTOSIS OF HEAD : TYPE OF NON - LANGERHANS CELLS HISTIOCYTOSIS [PDF]

Journal of Evolution of Medical and Dental Sciences, 2014
Papular histiocytosis of the head also known as benign cephalic histiocytosis is a rare, self-limiting histiocytosis that typically starts in early childhood. 1 Erythematous macules, papules and nodules develop on cheeks and spread to the forehead, earlobes and neck. Lesions are asymptomatic, gradually become reddish brown and may spread to involve the
Gaurav Murti, Anil K. Gupta
openaire   +1 more source

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   +4 more sources

A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations

Journal of Cutaneous Immunology and Allergy, 2023
Rosai–Dorfman disease (RDD) is a rare non‐Langerhans cell histiocytosis that was first described as sinus histiocytosis with massive lymphadenopathy by Rosai and Dorfman in 1969.
Shintaro Saito, Akihiko Uchiyama, Yayoi Shibusawa, Sei‐ichiro Motegi   +3 more
doaj   +1 more source

Adult Langerhans cell histiocytosis with pulmonary and colorectoanal involvement: a case report

Journal of Medical Case Reports, 2017
Background Langerhans cell histiocytosis is a rare systemic disease characterized by the abnormal overproduction of histiocytes that tend to infiltrate single or multiple organ systems leading to significant tissue damage. It mainly affects – by order of
Mohamad Jihad Mansour, Elias Mokbel, Eddy Fares, Janah Maddah, Fadi Nasr   +4 more
doaj   +1 more source

An unusual case of intracerebral Non-Langerhans cell histiocytosis with review of the literature [PDF]

Diagnostic Pathology, 2007
Conclusion This case shows the unusual manifestation of a primary intracerebral Non-Langerhans cell histiocytosis, which begins as a solid mass around the sellar region and shows a remarkable extension as a flat lining of inner and outer liquor spaces.
Mueller, K., Trippel, M., Berlis, Ansgar, Janzarik, W., Volk, B.   +4 more
openaire   +3 more sources

A case of Langerhans cell histiocytosis mimicking child abuse

The Turkish Journal of Pediatrics, 2016
Langerhans cell histiocytosis is a rare non-malignant disease with clinical heterogeneity. The disease may present with various clinical findings and may imitate many other conditions.
Şakire Başer, Yasemin Taşcı, Esin Boduroğlu, Asuman Gürkan, Umut Kaygusuz, Türkan Aydın-Teke, Zeynep Gökçe Gayretli-Aydın, Işıl Zaimoğlu, Ayşe Kaman, Gönül Tanır   +9 more
doaj   +1 more source

Non-Langerhans cell histiocytosis in a child with Kawasaki disease

BMJ Case Reports, 2009
Polymorphous skin rashes are one of the major presentations in children with Kawasaki disease. This report describes an unusual presentation of a skin rash (non-Langerhans cell histiocytosis) in a 4-month-old baby with resistance to intravenous immunoglobulin (IVIG) treatment and coronary artery dilatation.
Hong-Ren Yu, Kuender D. Yang, Chih-Chiang Wu, Tsung-Hsien Yang, Chi-Di Liang, Ho-Chang Kuo, Yi-Ju Chen   +6 more
openaire   +4 more sources