Results 211 to 220 of about 13,665 (250)
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Cytology of Canine Malignant Histiocytosis

Veterinary Clinical Pathology, 1994
Cytologic features of bone marrow, tissue, and abdominal fluid in seven cases of malignant histiocytosis in dogs are described, and histopathology, hematology, and serum biochemistry of the cases are reviewed. Diagnosis of malignant histiocytosis was confirmed by tissue morphology and immunohistochemistry; neoplastic cells in all cases had positive ...
Diane E., Brown   +4 more
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Malignant histiocytosis of the intestine

Digestive Diseases and Sciences, 1979
Four cases of malignant histiocytosis of the intestine (MHI) are described in detail, with emphasis on the clinical features and laboratory findings that may lead to a diagnosis. MHI is a rapidly progressive, usually fatal condition, which may occur in a setting of adult celiac disease or apparently spontaneously; all patients, however, have villous ...
J R, Hodges   +3 more
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Malignant Histiocytosis Simulating Granulomatous Disease

American Journal of Clinical Pathology, 1980
In its clinical presentation, malignant histiocytosis may mimic infections or hematologic neoplasms, and pathologically it may be mistaken for Hodgkin's disease, histiocytic lymphoma, or viral lymphadenitis. The case histories of three patients in whom malignant histiocytosis clinically and pathologically simulated granulomatous diseases are reported ...
R A, Sacher   +3 more
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Malignant Histiocytosis Presenting as Erythroderma

International Journal of Dermatology, 1990
A man presented witb a 2 montb bistory of raised temperature, malaise, weakness, intense itcbing, and skin lesions involving tbe trunk and extremities. Pbysical examination revealed generalized, large, well-defined erytbematous patcbes witb desquamated and licbenified surfaces. No bepatosplenomegaly and lympbadenopatby were observed.
A, Patrizi   +3 more
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Malignant histiocytosis in the oropharynx

Journal of Surgical Oncology, 1984
AbstractMalignant histiocytosis is characterized by systemic, progressive, and invasive proliferation of malignant histiocytes. The disorder is typically accompanied by fever, general fatigue, lymphadenopathy, and hepatosplenomegaly. A case of a 21‐year‐old woman with primary malignant histiocytosis of the oropharynx is reported.
H, Ogasawara   +5 more
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MALIGNANT HISTIOCYTOSIS

Hematology/Oncology Clinics of North America, 1998
Jean Gogusev, Christian Nezelof
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Therapy of Malignant Histiocytosis

1981
Rappaport in 1966 [10] introduced the term “malignant histiocytosis” to describe a disorder of “systemic, progressive, invasive proliferation of atypical histiocytes.” An identical disorder was observed by Scott and Robb-Smith in 1939 [11] and termed “histiocytic medullary reticulosis.” The most conspicuous clinical features of this disorder are ...
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Malignant Histiocytosis

American Journal of Clinical Pathology, 1994
S. V. Walsh, Charles Eugene Connolly
openaire   +3 more sources

Malignant histiocytosis of the intestine

The Journal of Pathology, 1985
Four cases of malignant histiocytosis of the intestine (MHI) are described in detail, with emphasis on the clinical features and laboratory findings that may lead to a diagnosis. MHI is a rapidly progressive, usually fatal condition, which may occur in a setting of adult celiac disease or apparently spontaneously; all patients, however, have villous ...
openaire   +2 more sources

Malignant histiocytosis

Cancer Nursing, 1978
S D, Palmer, K F, Carnes
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