Results 91 to 100 of about 3,979 (253)

Rosai-Dorfman Disease: A Clinico-pathological Presentation of Three Cases and Review of Literature [PDF]

Journal of Clinical and Diagnostic Research, 2018
Rosai-Dorfman Disease (RDD) or Sinus Histiocytosis with Massive Lymphadenopathy (SHML) is a rare histiocytic disorder of unknown aetiology which presents as a benign, self-limiting disease of phagocytic histiocytes occurring mainly in the first and ...
Francis Ikechukwu Ukekwe, Uchechukwu Obiora Ezomike, Osita Uchenna Ezenwosu, Christopher Bismarck Eke, Chibueze Onyekachi Nwokoro   +4 more
doaj   +1 more source

Diagnostics of Autoimmune Hepatitis Enabled by Non‐Invasive Clinical Proteomics

Alimentary Pharmacology &Therapeutics, Volume 62, Issue 9, Page 901-919, November 2025.
Mass‐spectrometry‐based proteomic analyses of paired liver‐plasma samples from patients with AIH enabled discovery of numerous proteins showing high diagnostic accuracy. Proteomics may constitute a novel non‐invasive diagnostic tool for AIH if validated in larger, age‐ and sex‐matched cohorts.
Anne‐Sofie Houlberg Jensen, Henriette Ytting, Annelaura Bach Nielsen, Mikkel Parsberg Werge, Elias Badal Rashu, Liv Eline Hetland, Mira Thing, Puria Nabilou, Johan Burisch, Anders Ellekær Junker, Lise Hobolth, Christian Mortensen, Flemming Tofteng, Flemming Bendtsen, Søren Møller, Mogens Vyberg, Reza Rafiolsadat Serizawa, Marie Winther‐Sørensen, Jesper Sloth Kellemann, Lise Lotte Gluud, Nicolai Jacob Wewer Albrechtsen   +20 more
wiley   +1 more source

Natural history and outcomes in drug induced autoimmune hepatitis [PDF]

, 2016
Aim: Drug-induced autoimmune hepatitis (DIAIH) remains poorly characterized. Our aim was to assess natural history and outcomes in DIAIH. Methods: This was a retrospective cohort study.
Alla, Alvarez, Andrade, Appleyard, Björnsson, Björnsson, Björnsson, Castiella, Castiella, Cohen, Danan, Feld, Heneghan, Heurgué, Kennedy, Kocman, Lawrenson, Licata, Lucena, MacGregor, Manns, Navarro, Roberts, Russo, Sakaan, Scully, Sharp, Shepherd, Sugimoto, Suzuki, Unzueta, Verma, Verma, Weiler-Normann   +33 more
core   +1 more source

Intrathoracic Rosai–Dorfman Disease in Elderly Patients: A Case Report

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Rosai–Dorfman disease (RDD), a rare form of histiocytosis, predominantly affects young individuals. Clinically categorized into nodal and extranodal subtypes, the disease primarily involves systemic lymph nodes with possible involvement of other organs.
JianFeng Xiao, Li Ma, Wei Cao
wiley   +1 more source

Purely cutaneous rosai-dorfman disease with immunohistochemistry

Indian Journal of Dermatology, 2013
Background: The cutaneous form of Rosai-Dorfman disease (RDD) is a rare entity that manifests solely with skin papules or nodules and does not present with the usual myriad of symptoms of classical RDD.
Uzma Farooq, Anna H Chacon, Vladimir Vincek, George W Elgart   +3 more
doaj   +1 more source

Recommendations for the standardization of bone marrow disease assessment and reporting in children with neuroblastoma; on behalf of the International Neuroblastoma Response Criteria Bone Marrow Working Group [PDF]

, 2017
BACKGROUND: The current study was conducted to expedite international standardized reporting of bone marrow disease in children with neuroblastoma and to improve equivalence of care.
Aronica, Beiske, Bielle, Bomken, Brodeur, Burchill, Bustin, Cai, Cheung, Cheung, Choi, Cohn, Favrot, Franklin, Hata, Ifversen, Kushner, Livak, Mehes, Mehes, Mills, Monclair, Moss, Nagai, Nakajima, Oppedal, Parsons, Reid, Reid, Ruijter, Schmittgen, Schroeder, Schumacher-Kuckelkorn, Seeger, Shimada, Stutterheim, Stutterheim, Swerts, Viprey, Viprey   +39 more
core   +1 more source

Autoimmune gastrointestinal complications in patients with Systemic Lupus Erythematosus: case series and literature review [PDF]

, 2016
The association of systemic lupus erythematosus (SLE) with gastrointestinal autoimmune diseases is rare, but has been described in the literature, mostly as case reports.
Agmon-Levin N, Ahmed QM, Akram S, Arnett FC, Bessone F, Breuer GS, Byun JY, Cabrera GE, Carmona-Fernandes D, Carone FA, Chebli JM, Chong WP, Chowdhary VR, Cortese AF, Cowling DC, Criş cov GI, Culp KS, D A Isenberg, De Jager PL, Denham JM, Dreiling DA, Dubois EL, Ebert EC, Efe C, Efe C, Einarsdottir E, Essaadouni L, Fernández Rodríguez AM, Ferreiros-Vidal I, Fina D, Floreani A, Freeman HJ, Gershwin ME, Gibson T, Grimbacher B, Gupta D, Hallegua DS, Hamed I, Han S, Harada K, Hennes EM, Her M, Homberg JC, Irving KS, Isenberg DA, Janssens P, Joske RA, Ju JH, Kapila N, Katsanos KH, Katsanos KH, Laing TJ, Lee C-K, Leggett BA, Leonard WJ, Levy C, Lohse AW, Ludvigsson JF, Mackay IR, Makol A, Matsumoto T, Medina F, Michalopoulos G, Miller MH, Miyazaki T, Muratori P, Nakou M, Nesher G, Netto AP, Nitzan O, Park SW, Pascual-Ramos V, Pisetsky DS, Pollak VE, Reifenstein EC, Rensch MJ, Reynolds JC, Rodriguez EA, Runyon BA, Rustgi AK, S Custódio Alves, S Fasano, Seelig R, Serrano López MC, Shapeero LG, Shizuma T, Shizuma T, Sparberg M, Steffan W, Sultan SM, Sánchez-Guerrero J, Takahashi A, Taourel P, Thomas JR, Tian X-P, van Hoek B, Vergani D, Vitali C, Yamashita H, Zheng R-H, Zizic TM, Zizic TM   +101 more
core   +1 more source

Think highly of immunoglobulin G4‐related chronic rhinosinusitis as a clinical entity in immunoglobulin G4‐related disease

Eye &ENT Research, Volume 2, Issue 3, Page 151-163, September 2025.
Abstract IgG4‐related chronic rhinosinusitis (IgG4‐related CRS) is gaining recognition among various specialized physicians. As a systemic disease involving multiple organs, IgG4‐related CRS is still not widely recognized as an independent clinical entity. Given the complexity of diagnosing autoimmune‐related multisystem diseases, early recognition and
Lianqi Wan, Luo Zhang, Yingshi Piao, Yuan Zhang   +3 more
wiley   +1 more source

Analysis of Hyperexpanded T Cell Clones in SARS‐CoV‐2 Vaccine‐Associated Liver Injury by Spatial Proteomics and Transcriptomics

Liver International, Volume 45, Issue 7, July 2025.
ABSTRACT Background and Aims SARS‐CoV‐2 vaccine‐associated liver injury (SVALI) is a rare event and its pathophysiology remains unclear. Previous studies have found an oligoclonal CD8+ T cell infiltrate and SARS‐CoV‐2 spike antigen‐specific T cells in the liver of patients with SVALI. Therefore, we aimed to characterise the immune infiltrate in a liver
Sarp Uzun, Asmita Pant, Ewelina Bartoszek, Paul Gueguen, Stefan Frei, Hélène Heusler, Ilaria Arborelli, Carl Philipp Zinner, Neşe Karadağ Soylu, Benedetta Terziroli Beretta‐Piccoli, Cumali Efe, Matthias S. Matter   +11 more
wiley   +1 more source

Clinical and Molecular Characteristics of Megakaryocytes in Myelodysplastic Syndrome

Global Medical Genetics
Objective Myelodysplastic syndrome (MDS) is a malignant clonal disorder of hematopoietic stem cells which is characterized by morphologic dysplasia.
Fangxiu Luo, Jialu Zhao, Yubao Chen, Zhenping Peng, Ran An, Yeling Lu, Jiaming Li   +6 more
doaj   +1 more source