Results 111 to 120 of about 9,549 (243)

Altano-axial subluxation with torticollis secondary to Langerhans cell histocytosis

Interdisciplinary Neurosurgery, 2017
Langerhans Cell Histiocytosis is a rare disease featuring aberrant proliferation of dendritic cells that can infiltrate the bony skeleton. The authors report a case of six-year-old female presenting with torticollis. She was found to have extensive lytic
Joshua Y. Chua, MD, Ji Min Ling, FRCS, Derrick W.Q. Lian, FRCPath, Mei Yoke Chan, FRCP, David C.Y. Low, FRCS, Sharon Y.Y. Low, PhD, FRCS   +5 more
doaj   +1 more source

Baby with neonatal systemic juvenile xanthogranuloma born within a cross-cousin marriage

Dermatologica Sinica, 2015
Juvenile xanthogranuloma is a non-Langerhans cell histiocytosis seen most commonly in childhood and adolescence. Extracutaneous involvement is rare. We report an interesting and extremely rare case of systemic (skin, lung, spleen, and colon) “juvenile ...
Hikmet Tekin Nacaroglu, Demet Can, Canan Sule Unsal Karkiner, Yontem Yaman, Hudaver Alper, Hulya Tosun Yildirim, Paul W. Bishop   +6 more
doaj   +1 more source

Rare Presentation of a Rare Orthopedic Pathology: Erdheim Chester Disease [PDF]

, 2017
In 1930, William Chester and pathologist Jakob Erdheim discovered the pathology currently known as Erdheim Chester disease. There are only approximately 249 histologically confirmed patients to have been diagnosed with this disease as noted in the ...
Samona J, Owen J, Martin S
core   +1 more source

Multiple cutaneous reticulohistiocytoma

Indian Journal of Dermatology, 2016
Multicentric reticulohistiocytosis is a rare non-Langerhans cell histiocytosis characterized in its full form by severe destructive arthritis, cutaneous nodules, and systemic manifestations.
Karishma D Hemmady, Shylaja S Someshwar, Hemangi R Jerajani   +2 more
doaj   +1 more source

Cytophagic Histiocytic Panniculitis (CHP) in a Patient with SLE Found after Autopsy: When a Rash Is "Complicated!" [PDF]

, 2019
Introduction: Cytophagic histolytic panniculitis (CHP) is a clinical disorder characterized by nodular panniculitis of the subcutaneous adipose tissue. It was first described in 1980 by Winkelmann.
Abbas, Hafsa, Aslam, Ahsan, Chilimuri, Sridhar, Niazi, Masooma, Saad, Muhammad   +4 more
core   +1 more source

Juvenile Xanthogranuloma: Case Report and Literature Review

International Medical Case Reports Journal, 2020
Sadegh Vahabi-Amlashi, Masoumeh Hoseininezhad, Zahra Tafazzoli Cutaneous Leishmaniasis Research Center, Mashhad University of Medical Sciences, Mashhad, IranCorrespondence: Zahra TafazzoliDepartment of Dermatology, Imam Reza Hospital, Ibn e Sina Street ...
Vahabi-Amlashi S, Hoseininezhad M, Tafazzoli Z   +2 more
doaj  

Employment Situation of Parents of Long-Term Childhood Cancer Survivors [PDF]

, 2016
BACKGROUND: Taking care of children diagnosed with cancer affects parents' professional life. The impact in the long-term however, is not clear. We aimed to compare the employment situation of parents of long-term childhood cancer survivors with control ...
Ansari, M., Kuehni, C.E., Mader, L., Michel, G., Rischewski, J., Rueegg, C.S., Swiss Paediatric Oncology Group (SPOG), Vetsch, J.   +7 more
core   +6 more sources

A Multidisciplinary Non-Invasive Approach to Monitor Response to Intravenous Immunoglobulin Treatment in Neurodegenerative Langerhans Cell Histiocytosis: A Real-World Study. [PDF]

, 2023
Irene Trambusti, Carmen Barba, Marzia Mortilla, Susanna Rizzi, Katiuscia Romano, Maria Luisa Coniglio, Ersilia Lucenteforte, Claudio Favre, Renzo Guerrini, Elena Sieni   +9 more
openalex   +1 more source

A young man with multifocal brainstem leptomeningeal disease

Brain Pathology, Volume 35, Issue 6, November 2025.
Burana Khiankaew, Pornphan Sae‐Sim, Pichet Termsarasab, Oranan Tritanon, Theeraphol Panyaping, Paisarn Boonsakan, Vichan Peonim, Virawudh Soontornniyomkij   +7 more
wiley   +1 more source

Unique Presentation of Rosai-Dorfman Disease as Concomitant Appendiceal and Rectal Masses with IgG4-Positive Plasma Cells Diagnosed by Core Needle Biopsy

Case Reports in Oncological Medicine, 2020
Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a rare non-Langerhans cell histiocytosis. We report a case of a 69-year-old male with concurrent appendiceal and rectal masses who underwent CT-guided percutaneous ...
Jenna J. Poldemann, Benjamin H. Hinrichs, Abouelmagd Makramalla   +2 more
doaj   +1 more source