نتایج جستجو برای: proliferative histiocytic disease

تعداد نتایج: 1516925  

2012
Ram Chandra Adhikari

Correspondence: Dr. Ram Chandra Adhikari, MD Consultant Pathologist, Department of Pathology, Om Hospital & Research Centre, Kathmandu, Nepal GPO Box: 2496 E-mail: [email protected] Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis is a benign, self limited condition with higher prevalence among Japanese and other Asiatic people. Though the cause of this disease remains unc...

کرامت, فریبا, جعفری, محمد , محمودی , سعید ,

Kikuchi’s disease or histiocytic necrotizing lymphadenitis is uncommon disease that first time was recognized in Japan . The etiology of disease is unknown. Clinical features consist with unilateral cervical lymphadenopathy , often with upper respiratory prodrome and associated in some patients with fever . More cases occur in women , commonly under 40 years of ag...

2018
Cristiano Claudino Oliveira Rafael Bispo Paschoalini Maria Aparecida Custódio Domingues

Histiocytic sarcoma (HS) is a rare malignant neoplasia of hematopoietic origin and unknown etiology. We studied three patients with histiocytic sarcoma reviewing the morphological and immunohistochemical aspects. We evaluated in particular, if apoptosis may be unbalanced in this disease. All cases have morphological and immunohistochemical features consistent with the diagnosis of histiocytic s...

Journal: :Journal of clinical pathology 1991
E Backé R Schwarting J Gerdes M Ernst H Stein

A new monoclonal antibody Ber-MAC3 is reported. It recognises a formol sensitive epitope of a not yet clustered monocyte/macrophage specific 140 kilodalton glycoprotein that is expressed on the cell surface and in the cytoplasm. In 30 cases of acute and chronic leukaemia, Ber-MAC3 staining was restricted to 15 myeloid leukaemias of M4 and M5 types. The tumour cells of two cases of true histiocy...

Journal: :Haematologica 2006
Nathalie Gaspar Pascaline Boudou Julien Haroche Bertrand Wechsler Eric Van Den Neste Khe Hoang-Xuan Zahir Amoura Remy Guillevin Julien Savatovski Nabih Azar Jean-Charles Piette Véronique Leblond

We postulated that high-dose chemotherapy (HDC) followed by peripheral autologous hematopoietic stem cell transplantation might help to control refractory central nervous system (CNS) histiocytic disorders. Six patients with histiocytic CNS involvement were treated in this way. Two patients achieved non-active disease status, although one relapsed at 84 months. Two patients had regressive disea...

Journal: :Journal of clinical pathology 1982
K Aozasa

Nasal biopsy findings in malignant histiocytosis presenting clinically as lethal midline granuloma are characterised by necrosis and infiltration of atypical histiocytic cells with a diffuse positive reaction for non-specific esterase. This cellular character was common to midline malignant reticulosis, and midline malignant reticulosis and malignant histiocytosis are thought to be the same dis...

Journal: :Journal of clinical pathology 1977
L Michaels M M Gregory

In a histological study of biopsy and postmortem material from 30 cases of nasal disease in which a clinical diagnosis of 'midline granuloma' or Wegener's granuloma had been given, we selected 10 cases on the basis of the presence of widespread coagulative necrosis and atypical cells. Evidence is provided that such changes represent a malignant neoplasm of histiocytic lymphoma type. Local invas...

Milen Minkov,

Diseases of the monocyte, macrophage and dendritic cell system are referred to as histiocytoses. Based on improved understanding of their pathobiology and molecular background histiocytoses have been recently re-classified into five groups. Nevertheless, for practical reasons the histiocytoses are grouped into: Langerhans cell histiocytosis (the most common entity), hemophagocytic lymphohistioc...

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