Results 221 to 230 of about 13,346 (268)
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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.
Masao Mitsunobu   +5 more
openaire   +3 more sources

A Case of Malignant Histiocytosis

Ophthalmologica, 1984
Malignant histiocytosis, presenting initially with swelling and subcutaneous tumor in the lid, was reported in a 14-year-old boy. The diagnosis of malignant histiocytosis was made on the basis of light- and electron-microscopic findings.
Norio Katsumori   +3 more
openaire   +3 more sources

Malignant histiocytosis in a cat

Journal of the American Veterinary Medical Association, 1993
A 13-year-old male domestic shorthair cat was found to have normocytic hypochromic regenerative anemia, lymphopenia, eosinopenia, thrombocytopenia, hyperglycemia, hyperbilirubinemia, and a prolonged activated partial thromboplastin time. Transfusions of packed RBC failed to maintain the PCV above 13% for > 8 hours. The cat was euthanatized. At necropsy,
E A, Court   +3 more
openaire   +2 more sources

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 ...
Gregory K. Ogilvie   +4 more
openaire   +3 more sources

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.
Annalisa Patrizi   +3 more
openaire   +2 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   +3 more sources

Polymyositis Associated With Malignant Histiocytosis

JAMA: The Journal of the American Medical Association, 1981
SINCE Wagner's original description in 1863, dermatomyositis has been associated with different neoplastic conditions, including leukemias and lymphomas. 1-4 Thus far, we have been unable to find any other report of polymyositis associated with malignant histiocytosis (MH).
Javier Rivera   +5 more
openaire   +3 more sources

Combination Chemotherapy of Malignant Histiocytosis

Acta Haematologica, 1979
Three patients with malignant histiocytosis treated with combination chemotherapy are reported. Induction treatment included bleomycin, adriamycin, cyclophosphamide, vincristine and prednisone (BACOP). Complete response was obtained in one patient who is alive and well 32 months after diagnosis.
J.M. Lang   +5 more
openaire   +3 more sources

Malignant histiocytosis

Klinische Wochenschrift, 1980
Diagnosis of malignant histiocytosis (MH) was confirmed in 16 patients. Stage at diagnosis was I-II in nine, and III-IV in seven patients. Porr prognosis and "B",-symptoms were correlated to advanced stages. Bone marrow biopsy proved most useful to verify organ involvement.
P. Meister, Dieter Huhn, W. Wilmanns
openaire   +3 more sources

Malignant lymphoma and erythrophagocytosis simulating malignant histiocytosis

The American Journal of Medicine, 1983
Six patients with malignant lymphoma are described, in whom a syndrome that mimicked malignant histiocytosis clinically and pathologically developed as a terminal event. The clinical course was characterized by hepatosplenomegaly, fever, and a rapid fall in all hematologic counts.
Maria Tsokos   +4 more
openaire   +3 more sources

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