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Cancer, 1983
The clinical features, therapy, and hospital course of ten consecutive patients with malignant histiocytosis (MH) are presented. The value of bone marrow aspiration for the diagnosis is discussed. The patient's performance status as described in this report by the organ dysfunction score may predict survival and response to chemotherapy. The literature
D W, Esseltine +2 more
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The clinical features, therapy, and hospital course of ten consecutive patients with malignant histiocytosis (MH) are presented. The value of bone marrow aspiration for the diagnosis is discussed. The patient's performance status as described in this report by the organ dysfunction score may predict survival and response to chemotherapy. The literature
D W, Esseltine +2 more
+7 more sources
Plastic and Reconstructive Surgery, 1986
Malignant histiocytosis, also known as histiocytic medullary reticulosis, is a rare neoplasm of malignant histiocytes. Clinical findings include fever, weight loss, hepatosplenomegaly, lymphadenopathy, anemia, thrombocytopenia, and a rapidly worsening course.
M S, Stone, J A, Tschen
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Malignant histiocytosis, also known as histiocytic medullary reticulosis, is a rare neoplasm of malignant histiocytes. Clinical findings include fever, weight loss, hepatosplenomegaly, lymphadenopathy, anemia, thrombocytopenia, and a rapidly worsening course.
M S, Stone, J A, Tschen
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The Journal of Dermatology, 1988
AbstractThree patients with multiple skin nodules on the trunk and extremities showed hyperpyrexia, lymphadenopathy, pancytopenia, abnormal liver function, and terminal hemorrhagic diathesis. Histologically, the deep dermis and subcutaneous fat contained dense infiltrates of atypical erythropagocytic histiocytes and lymphoid cells.
M H, Chen +4 more
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AbstractThree patients with multiple skin nodules on the trunk and extremities showed hyperpyrexia, lymphadenopathy, pancytopenia, abnormal liver function, and terminal hemorrhagic diathesis. Histologically, the deep dermis and subcutaneous fat contained dense infiltrates of atypical erythropagocytic histiocytes and lymphoid cells.
M H, Chen +4 more
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Mayo Clinic Proceedings, 1998
To attempt to distinguish cases of true malignant histiocytosis from the clinical syndromes of so-called malignant histiocytosis with use of recent methods.We retrospectively studied the laboratory data and clinical course of Mayo patients who had clinical syndromes of so-called malignant histiocytosis and reviewed available paraffin-embedded tissue ...
W, Mongkonsritragoon +2 more
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To attempt to distinguish cases of true malignant histiocytosis from the clinical syndromes of so-called malignant histiocytosis with use of recent methods.We retrospectively studied the laboratory data and clinical course of Mayo patients who had clinical syndromes of so-called malignant histiocytosis and reviewed available paraffin-embedded tissue ...
W, Mongkonsritragoon +2 more
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Current Opinion in Hematology, 2001
Until recently, malignant histiocytosis was a clearly defined clinical entity marked by fever, progressive wasting, lymphadenopathy, hepatosplenomegaly, and pancytopenia. However, for many years the morphologic findings in this disease continued to cause a great deal of controversy.
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Until recently, malignant histiocytosis was a clearly defined clinical entity marked by fever, progressive wasting, lymphadenopathy, hepatosplenomegaly, and pancytopenia. However, for many years the morphologic findings in this disease continued to cause a great deal of controversy.
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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.
D, Huhn, P, Meister, W, Wilmanns
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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.
D, Huhn, P, Meister, W, Wilmanns
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Malignant Histiocytosis After Lymphoblastic Lymphoma
Archives of Pediatrics & Adolescent Medicine, 1983Malignant histiocytosis developed in a 19-year-old boy 3 1/2 years after the initial diagnosis of lymphoblastic lymphoma of T-cell origin. The experience with this young adult suggests that a close surveillance of the survivors of lymphoma is mandatory, and a prompt biopsy of enlarged lymph nodes in patients treated for lymphoma should be a routine ...
T H, Kim +4 more
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Malignant lymphoma and erythrophagocytosis simulating malignant histiocytosis
The American Journal of Medicine, 1983Six 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.
E S, Jaffe +4 more
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