Results 111 to 120 of about 25,153 (346)

Analysis of pathological features of lymph node in adult-onset Still disease

Zhongguo Linchuang Yixue
ObjectiveTo summarize the pathological morphological features, diagnosis, and differential diagnosis of adult-onset Still disease (AOSD), and to improve clinical understanding of the disease.
Ting CHEN, Yingyong HOU, Xiaowen GE
doaj   +1 more source

DIFFUSION NORMOLIPIDEMIC FLAT XANTHOMA, ASSOCIATED WITH HYPOCHROMIC ANEMIA. DESCRIPTION OF THE CASES

Vestnik Dermatologii i Venerologii, 2017
The diffuse plane xanthoma (DPX) belongs to the class II of histiocytosis arising from the dermal dendritic cells (Histiocyte Society). The dominate role in the formation of the disease in the skin plays an accumulation of phagocytic immune complexes of ...
V. D. Elkin, T. G. Sedova, E. V. Plotnikova, I. D. Kuznetsov, M. U. Novoselova   +4 more
doaj   +1 more source

Visceral leishmaniasis, hypertriglyceridemia and secondary hemophagocytic lymphohistiocytosis [PDF]

, 2016
Visceral leishmaniasis (VL), a protozoan disease, is 100 % fatal if left untreated. Anemia is common in VL which plays a role in expression of clinically overt VL disease.
Barberi, G., Cama, V., CASCIO, ANTONIO, COLOMBA, Claudia, DI CARLO, Paola, Famà, F., Iaria, C., SCARLATA, Francesco   +7 more
core   +2 more sources

Hemophagocytic lymphohistiocytosis presenting with acute liver failure and central nervous system involvement in early infancy

Indian Journal of Pathology and Microbiology, 2018
Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal and likely underdiagnosed disease characterized by unregulated histiocyte proliferation, hypercytokinemia and hemophagocytosis, causing life-threatening tissue damage and organ failure.
Mukesh Kumar, Nirupama Kothari, B D Gupta, Neeraj Gupta   +3 more
doaj   +1 more source

The cytogenesis of ascitic pha­gocytes [PDF]

, 1959
Judging from our vital observation conducted mainly by tissue culture, it was firmly demonstrated that ascitic phagocytes are not histiocytes but they are the cells closely related to monocytes and that the sites of the genesis are the milky spots of the
Fukuda, Genjiro, Kamura, Junta, Kitajima, Koichi, Kotani, Saburo, Ofuji, Tadashi, Ota, Zensuke, Yamachika, Yukio   +6 more
core   +1 more source

Diagnosing Systemic Mastocytosis: State of the Art

International Journal of Laboratory Hematology, EarlyView.
ABSTRACT With the advent of effective multikinase and selective tyrosine kinase inhibitors in systemic mastocytosis, diagnosing this rare disease has been critical to improving patient morbidity and mortality. This state‐of‐the‐art review interprets the international diagnostic criteria, including differences between the WHO 5th edition classification ...
Anton Rets, Tracy I. George
wiley   +1 more source

Langerhans cell histiocytosis: unusual bone marrow infiltration—report of 2 cases in Ecuador

Frontiers in Medicine
Langerhans cell histiocytosis (LCH) is a histiocytic neoplasm characterized by the abnormal proliferation of Langerhans cells. Bone marrow (BM) involvement is associated with high-risk disease and poor survival.
Paulina Santana, Paulina Santana, Marlon Arias-Intriago, Juan S. Izquierdo-Condoy   +3 more
doaj   +1 more source

Unique presentation of T-cell/histiocyte-rich large B cell lymphoma complicated with hemophagocytic lymphohistiocytosis: Case report and review of the literature [PDF]

Journal of Medical Biochemistry
Hemophagocytic lymphohistiocytosis (HLH) is a rare, lifethreatening hyperinflammatory disorder characterized by dysfunction of NK cells and cytotoxic lymphocytes.
Pešić Andrej, Vuković Vojin, Kozarac Sofija, Otašević Vladimir, Bibić Tamara, Mihaljević Biljana, Antić Darko   +6 more
doaj   +1 more source

Immune cell infiltration correlates with intestinal permeability, inflammation, and gastrointestinal symptoms in type 1 diabetes

Journal of Diabetes Investigation, EarlyView.
In individuals with type 1 diabetes, immune cell infiltration in the colon mucosa tended to correlate with fecal and systemic markers of intestinal permeability and inflammation, as well as gastrointestinal symptoms. These findings suggest that low‐grade gut immune activation might link the intestinal barrier dysfunction with systemic endotoxin ...
Polina Zalizko, Reinis Isaks, Leonora Pahirko, Aleksejs Fedulovs, Eduards Krustins, Jurijs Nazarovs, Sergejs Dubencovs, Hanne Salmenkari, Markku Lehto, Kaspars Jēkabsons, Una Riekstiņa, Per‐Henrik Groop, Niina Sandholm, Jeļizaveta Sokolovska   +13 more
wiley   +1 more source

Extranodal Rosai-Dorfman disease of the bone treated with surgery and radiotherapy

Rare Tumors, 2014
Rosai-Dorfman disease (RDD) is a rare, benign histiocyte disorder originally described by Rosai and Dorfman in 1969 as sinus histiocytosis with massive lymphadenopathy.
Nitesh N. Paryani, Larry C. Daugherty, Mary I. O’Connor, Liuyan Jiang   +3 more
doaj   +1 more source