Results 41 to 50 of about 29,211 (229)
Histiocytic cytophagic panniculitis [PDF]
Postgraduate Medical Journal, 1990 Summary A 33 year old man developed fever, malaise, jaundice, pancytopenia, coagulation abnormalities, hepatomegaly, pleural effusions and a subcutaneous lump. Biopsies revealed a lobular panniculitis with the presence of cytophagic histiocytes; erythrophagocytosis was also demonstrated in the liver and bone marrow.
D A, Hilton, B P, O'Malley, S T, Durrant
openaire +2 more sources
Xanthogranulomatous Oophoritis- A Rare Inflammatory Lesion [PDF]
Journal of Krishna Institute of Medical Sciences University, 2013 Xanthogranulomatous inflammation is a specialform of chronic inflammation that is destruc-tive of affected organ. Xanthogranulomatous in-flammation of ovary and fallopian tube is an un-common entity and it is usually known to oc-cur in the kidney and ...
Mahesh H Karigoudar +3 more
doaj
Primary unifocal thymic Rosai-Dorfman disease: an extremely rare challenge in diagnostic practice
Journal of Cardiothoracic Surgery, 2023 Rosai-Dorfman disease (RDD) is currently considered a group of neoplastic diseases of unknown etiology, with monoclonal proliferation of histiocytes, showing unique histopathologic features and varying clinical presentation.
Qian Liu +4 more
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Indian Journal of Endocrinology and Metabolism, 2011 Gaucher′s disease (GD) is the most common amongst the various disorders classified under the lysosomal storage disorders. GD is a model for applications of molecular medicine to clinical delineation, diagnosis, and treatment.
Vijay Bohra, Velu Nair
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histiocytic Necrotizing Lymphadenitis
Apollo Medicine, 2006 We are presenting a case of histiocytic necrotizing lymphadenitis (Kikuchi disease), which is characterized by involvement of lymph nodes, skin, liver and spleen. A 21-year-old girl presented with 27 days history of prolonged fever, left cervical painless lymphadenitis and maculo-papular skin rashes.
Vijay Kumar Aneja +2 more
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Xanthogranulomatous endometritis: A benign uncommon masquerader of malignancy
Journal of Mid-Life Health, 2019 Xanthogranulomatous endometritis is an uncommon benign lesion characterized by the destruction of endometrium and replacement by the sheets of foamy histiocytes, lymphocytes, plasma cells, multinucleated giant cells, fibrosis, calcification, and ...
Vipra Malik +3 more
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Indian Journal of Pathology and Microbiology, 2020 Sea-blue histiocytes in bone marrow can be associated with a number of conditions and have indeed often been reported in Niemann-Pick diseases, mostly in Niemann-Pick type B, but also Niemann-Pick type C.
Li Wang +5 more
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Clinical Images: A thorn injury, a sea‐borne culprit, and a tenosynovitis dilemma
Arthritis &Rheumatology, EarlyView.
Jacopo Ciaffi +8 more
wiley +1 more source
Cutaneous Rosai‐Dorfman Disease With MAP2K1 Mutation Treated With Encorafenib and Binimetinib
JEADV Clinical Practice, EarlyView.ABSTRACT Rosai‐Dorfman disease (RDD) is a rare histiocytic disorder with unifocal to multisystemic involvement. Activating mutations in the MAPK/ERK pathway can occur in up to 50% of RDD cases. We report a case of cutaneous RDD (C‐RDD) with facial and truncal lesions harboring an activating MAP2K1 (MEK1) mutation that showed a complete response to a ...
Melike Ak +2 more
wiley +1 more source
Pediatric Investigation, EarlyView.This study elucidates the critical pathogenic mechanisms of pediatric Epstein–Barr virus‐associated hemophagocytic lymphohistiocytosis (EBV‐HLH), where EBV infection triggers a cytokine storm leading to immune cell hyperactivation and tissue damage. Dynamic plasma biomarkers (EBV‐DNA, ferritin, and interferon‐γ) effectively predict treatment response ...
Feifei Liu +9 more
wiley +1 more source