Results 101 to 110 of about 9,762 (221)

Caso para diagnóstico Case for diagnosis

Anais Brasileiros de Dermatologia, 2011
Relatamos um caso de histiocitose cefálica benigna em uma criança do sexo masculino, de um ano e três meses de idade que desenvolveu múltiplas pápulas na região malar bilateralmente, sem outros comemorativos associados.
Maria de Fátima Guimarães Scotelaro Alves, Carolina Villela da Rocha Miranda, Clarissa de Souza Abreu, Marcela Duarte Villela Benez, Luna Azulay-Abulafia   +4 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

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

Better a Broader Diagnosis Than a Misdiagnosis: The Study of a Neoplastic Condition in a Male Individual who Died in Early 20th Century (Coimbra, Portugal) [PDF]

, 2013
The paleopathological record of neoplastic conditions in the past is considered scarce. The detection of tumours in ancient populations is hindered by the quality and quantity of signs visible on the skeleton, the methodological approach, the ...
Cunha, Eugénia, Marques, Carina, Santos, Ana Luísa   +2 more
core   +2 more sources

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

Successful treatment of non-Langerhans cell histiocytosis with the MEK inhibitor trametinib: a multicenter analysis. [PDF]

Blood Adv, 2023
Aaroe A, Kurzrock R, Goyal G, Goodman AM, Patel H, Ruan G, Ulaner G, Young J, Li Z, Dustin D, Go RS, Diamond EL, Janku F.   +12 more
europepmc   +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  

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

Novel actionable ROS1::GIT2 fusion in non-Langerhans cell histiocytosis with central nervous system involvement. [PDF]

Acta Neuropathol, 2023
Bedics G, Csóka M, Reiniger L, Varga E, Liptai Z, Papp G, Bekő A, Cervi C, Bödör C, Scheich B.   +9 more
europepmc   +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