Results 61 to 70 of about 1,339 (137)
The Rosai Dorfman Syndrome–The Report of A Rare Case [PDF]
Journal of Clinical and Diagnostic Research, 2013 Rosai Dorfman syndrome known as Sinus Histiocytosis with Massive Lymphadenopathy (SHML) is an uncommon benign systemic histio-proliferative disease which affects lymph nodes, most often those of the neck (cervical lymphadenopathy). The characteristic
Snehalatha R +3 more
doaj +1 more source
Role of liver biopsy in the management of idiosyncratic DILI
Liver International, Volume 45, Issue 3, March 2025.Abstract Drug‐induced liver injury (DILI) presents unique challenges in clinical practice. While some types of DILI are mild and resolve quickly after removing the drug, other situations are more complex, with competing aetiologies or underlying liver disease.
David E. Kleiner
wiley +1 more source
Immune cell pathology in rabbit hemorrhagic disease [PDF]
Veterinary World, 2019 Aim: The aim of this research was to study the effect of rabbit hemorrhagic disease virus (RHDV) on the host immune response by examining the cellular composition/pathology of lymphoid organs and serum levels of tumor necrosis factor-alpha (TNF-α) and ...
Anna Babken Semerjyan +11 more
doaj +1 more source
Case Reports in Hematology, Volume 2025, Issue 1, 2025.Gray platelet syndrome (GPS) is a rare inherited platelet disorder characterized by the presence of gray platelets on blood smears, resulting from a deficiency of α‐granules. The thrombocytopenia presents in a spectrum of bleeding tendencies, varying among different patients.
Muhammad Takhman +5 more
wiley +1 more source
Mediators of Inflammation, Volume 2025, Issue 1, 2025.Primary myelofibrosis (PMF) is a clonal myeloproliferative neoplasm (MPN) stemming from hematopoietic stem and progenitor cells (HSPCs), frequently associated with mutations in Janus kinase signal transducer (JAK2), calreticulin (CALR), or thrombopoietin receptor (MPL).
Meng Chen +5 more
wiley +1 more source
Rosai Dorfman disease- A rare entity: Case report in North Indian male
Asian Journal of Medical Sciences, 2014 Rosai Dorfman disease is a rare disease characterized by histiocytic proliferation of lymph node in young adults. We present here the case of a 67 years old Indian male presenting with lymphadenopathy and pyrexia of unknown origin for 16 months duration.
Ankur Baruah
doaj +1 more source
Journal of Cutaneous Pathology, Volume 51, Issue 12, Page 942-947, December 2024.Abstract Rarely, Rosai–Dorfman disease (RDD) manifests exclusively in the skin, typically as nodules on the trunk and extremities. Recognition of characteristic histopathologic features enables diagnosis of RDD. A 55‐year‐old female presented with a 7‐year history of cutaneous nodules involving the trunk and extremities. A prior skin biopsy specimen at
Joseph Gillam +6 more
wiley +1 more source
Scientific Reports, 2016 The Gray Platelet Syndrome (GPS) is a rare inherited bleeding disorder characterized by deficiency of platelet α-granules, macrothrombocytopenia and marrow fibrosis.
C. D. Di Buduo +9 more
semanticscholar +1 more source
A Rare Case of Primary Intraparenchymal Rosai‐Dorfman Disease
iRADIOLOGY, Volume 3, Issue 5, Page 370-371, October 2025.
Lin Chen, Rui Zhou
wiley +1 more source
Idiopathic multicentric Castleman disease with marrow fibrosis and extramedullary hematopoiesis
European Journal of Haematology, Volume 113, Issue 6, Page 833-841, December 2024.Abstract Background Idiopathic multicentric Castleman disease (iMCD) is a rare inflammatory disorder mediated by excessive proinflammatory cytokine signaling, most notably by interleukin 6 (IL‐6). IL‐6‐induced extramedullary hematopoiesis (EMH) has been reported in murine models of iMCD. Herein we present four cases of iMCD with EMH in humans.
Marley Blommers +10 more
wiley +1 more source