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Postchemotherapy Histiocyte-Rich Pseudotumor of the Spleen Simulating Residual Disease in a Patient With Non-Hodgkin Lymphoma on FDG PET/CT.

Clinical Nuclear Medicine, 2019
A 64-year-old man was treated with multiagent chemotherapy owing to high-grade non-Hodgkin lymphoma presenting as a bulky disease involving the spleen.
N. Hod   +5 more
semanticscholar   +1 more source

Histiocytic Diseases

Veterinary Clinics of North America: Small Animal Practice, 2023
Canine cutaneous histiocytomas originate from Langerhans cells. Multiple histiocytomas are referred to as cutaneous Langerhans cell histiocytosis. Feline pulmonary Langerhans cell histiocytosis causes respiratory failure owing to extensive lung infiltration. Localized and disseminated histiocytic sarcomas usually arise from interstitial dendritic cells.
openaire   +2 more sources

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
openaire   +2 more sources

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
openaire   +3 more sources

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.
openaire   +3 more sources

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
openaire   +2 more sources

Histiocytic lymphoma in the mouse

Leukemia Research, 1980
Abstract This investigation studied the occurrence, distribution and morphology; and the transplantation, ultrastructural and in vitro characteristics of histiocytic lymphoma in the BALB/c and C57BL/6 strains of mice. The disease was more common in aged females of both strains.
Charles H. Frith   +6 more
openaire   +4 more sources

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.
Najmun Nahar   +9 more
openaire   +4 more sources

Histiocytic proliferations

Seminars in Diagnostic Pathology, 2016
The study of Histiocytic lesions has been a passion of Pepper Dehner over the years. He has contributed several case series and reviews on various categories of these diseases for over 4 decades, with his earliest articles in the 1970s. He has written on all aspects of the disease including seminal articles on Langerhans cell histiocytosis (LCH) and ...
openaire   +2 more sources

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 ...
Frederick G. Zak, Emanuel Rubin
openaire   +3 more sources

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