Results 261 to 270 of about 58,815 (317)
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Dermatology, 1980
Histiocytosis X is characterized by a proliferation of cytologically benign histiocytes and occurs in a severe form (type 1) with a short course and poor prognosis and a milder form (type 2) with a protracted course and favorable prognosis. Otolaryngologists will encounter the type 2 form of the disease and must include it in the differential diagnosis
Harold F. Schuknecht, Spyros Papaspyrou
+7 more sources
Histiocytosis X is characterized by a proliferation of cytologically benign histiocytes and occurs in a severe form (type 1) with a short course and poor prognosis and a milder form (type 2) with a protracted course and favorable prognosis. Otolaryngologists will encounter the type 2 form of the disease and must include it in the differential diagnosis
Harold F. Schuknecht, Spyros Papaspyrou
+7 more sources
Current understanding and management of pulmonary Langerhans cell histiocytosis
Thorax, 2017 Robert Vassallo +2 more
exaly +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
FDG PET‐CT in pediatric Langerhans cell histiocytosis
Pediatric Blood & Cancer, 2020Langerhans cell histiocytosis (LCH) in pediatric patients presents with single‐system or multisystem disease. Accurate staging is essential for selecting the most appropriate therapy ranging from local surgery to chemotherapy.
S. Jessop +4 more
semanticscholar +1 more source
Human Pathology, 1983
To clarify salient issues pertaining to histiocytosis X--a syndrome that includes Letterer-Siwe disease, Hand-Schuller-Christian disease, and eosinophilic granuloma--the authors review the epidemiologic data and the histologic, morphologic, and clinical bases for diagnosis and prognosis. Histiocytes are defined and their possible histogenesis outlined,
B E, Favara, R C, McCarthy, G W, Mierau
openaire +2 more sources
To clarify salient issues pertaining to histiocytosis X--a syndrome that includes Letterer-Siwe disease, Hand-Schuller-Christian disease, and eosinophilic granuloma--the authors review the epidemiologic data and the histologic, morphologic, and clinical bases for diagnosis and prognosis. Histiocytes are defined and their possible histogenesis outlined,
B E, Favara, R C, McCarthy, G W, Mierau
openaire +2 more sources
American Journal of Surgical Pathology, 2020
Originally described as a systemic self-limiting disease in infancy, the spectrum of ALK-positive histiocytosis has recently been broadened to include localized diseases in older children and young adults.
J. Kashima +6 more
semanticscholar +1 more source
Originally described as a systemic self-limiting disease in infancy, the spectrum of ALK-positive histiocytosis has recently been broadened to include localized diseases in older children and young adults.
J. Kashima +6 more
semanticscholar +1 more source
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
openaire +2 more sources
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
openaire +2 more sources
Leukemia and Lymphoma, 2020
Histiocytoses are one of the ultimate diagnostic challenges that every physician face at least once in his/her life. Giving their protean manifestation and differentiated therapeutic needs, histiocytosis requires extensive characterization and ...
A. Bonometti
semanticscholar +1 more source
Histiocytoses are one of the ultimate diagnostic challenges that every physician face at least once in his/her life. Giving their protean manifestation and differentiated therapeutic needs, histiocytosis requires extensive characterization and ...
A. Bonometti
semanticscholar +1 more source