Results 211 to 220 of about 31,396 (267)
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Histiocytic Syndromes

Dermatologic Clinics, 1989
The histiocytic syndromes are currently divided into two major categories: Langerhans cell histiocytosis and non-Langerhans cell histiocytosis. The disease entities recognized under these categories are discussed. The discussion includes clinical features, histopathology, and treatment.
S S, Raimer, E, Hollabaugh
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Histiocytic endometritis

Histopathology, 1980
Two cases of histiocytic endometritis are described, both characterized by total replacement of the endometrium with sheets of lipid‐containing histiocytic cells. This condition appears to be a rare complication of cervical occlusion and it is suggested that the histiocytic reaction occurs as a response to a haematometra.
C H, Buckley, H, Fox
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Histiocytic Sarcomas

Leukemia & Lymphoma, 1995
In this study a review of malignancies classified as histiocytic in the literature is given. The available data suggest that a distinction can be made between three main categories, i.e., follicular dendritic cell (FDC) sarcomas, Langerhans' cell/interdigiting reticulum cell (LC/IRC) sarcomas and histiocytic sarcomas (HS) which are unrelated to ...
A F, Lauritzen, E, Ralfkiaer
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The Histiocyte

Archives of Dermatology, 1986
Certain terms, by an enigmatic stubbornness, persist long after their usefulness is ended. Such is the case of thehistiocyte—particularly in dermatology and dermatopathology.1Reports of the demise of thehistiocyte(italics to emphasize my disfavor), could not be too greatly exaggerated.
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The Histiocytic Marker PG-M1 Is Helpful in Differentiating Histiocytes and Histiocytic Tumors From Melanomas

Applied Immunohistochemistry & Molecular Morphology, 2002
Previous studies have shown that immunohistochemical stains for histiocytes are immunoreactive for melanomas. Accordingly, their value in differentiating histiocytes and histiocytic lesions from melanomas was questioned. PG-M1, the most specific histiocytic marker, was not evaluated in these studies. Our aims were to assess the reactivity of PG-M1 with
Gabriel M, Groisman   +2 more
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Confluent Granulomas and Ulcers Lined by Epithelioid Histiocytes: New Ideal Method for Differentiation of ITB and CD? A Meta Analysis

open access: yesPLoS ONE, 2014
BackgroundThere are few widely accepted criteria other than caseation, which has low sensitivity, for differentiating intestinal tuberculosis (ITB) and Crohn's disease (CD).ObjectiveWe performed a meta-analysis to evaluate the use of confluent granulomas
Juan Du   +3 more
exaly   +2 more sources

Cutaneous true histiocytic malignancy: True histiocytic lymphoma

Journal of the American Academy of Dermatology, 2004
True histiocytic malignancies (THM) are controversial disorders that are being re-evaluated with modern cellular and molecular biology techniques. True histiocytic lymphoma (THL) is a low-incidence, poor-prognosis THM. It mainly affects the skin, gastrointestinal tract, and bone tissues.
Myriam, Chaín   +7 more
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Histiocytic sarcoma of the brain

Journal of Clinical Neuroscience, 2012
Histiocytic sarcoma is a rare malignant neoplasm of the lympho-hematopoietic system that usually occurs in the skin, lymph nodes and intestinal tract. We present a 36-year-old woman with a rare histiocytic sarcoma with isolated central nervous system (CNS) involvement of multifocal circumscribed lesions.
Boadle, Rose A.   +7 more
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Histiocytic medullary reticulosis

The American Journal of Medicine, 1961
Abstract The case presented fulfills the clinical and morphologic requirements of histiocytic medullary reticulosis as laid down by Bodley Scott and Robb-Smith [1]. This invariably and apparently rapidly fatal disease of adults is characterized morphologically by a diffuse proliferation of phagocytic histiocytes and their precursors in lymph nodes ...
F G, ZAK, E, RUBIN
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Histiocytic syndromes: A review

Journal of the American Academy of Dermatology, 1985
Histiocytoses represent a large, puzzling group of rare skin diseases. The purpose of this review is to schematically outline the clinical, histologic, and ultrastructural features of the most important histiocytic syndromes and to provide the pertinent differential diagnoses.
F, Gianotti, R, Caputo
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