langerhans cell histiocytosis following hodgkin lymphoma: a case report from iran
نویسندگان
چکیده
the occurrence of langerhans cell histiocytosis (lch) in a patient with lymphoma is an indication of a probable relationship between them. the two conditions have similarities both clinically and histopathologically. occurrence of these two conditions in the same patient, particularly not simultaneously, is rare. according to different management and treatment of these conditions, exact histopathologic evaluation and even using immunohistochemistery (ihc) can prevent misdiagnosis. in this report, a 10 year old boy presented who afflicted with lch 3 years after diagnosis and treatment of mixed cellularity hodgkin lymphoma. keywords: hodgkin disease, langerhans cell histiocytosis, immunohistochemistry. normal 0 false false false microsoftinternetexplorer4
منابع مشابه
Langerhans Cell Histiocytosis Followed by Hodgkin Lymphoma: A Case Report
Langerhans cell histiocytosis (LCH) is a rare neoplasm defined as the proliferation of bone marrow langerhans cells, which is a kind of dendritic cells. The major pathological features of LCH are expression of CD1a and S100 as well as Birbeck granules. Its presentation can differ from a mild bone lesion to a multi-systemic evolved malignant neoplasm; however, the latter outcome is almost rare. ...
متن کاملlangerhans cell histiocytosis followed by hodgkin lymphoma: a case report
langerhans cell histiocytosis (lch) is a rare neoplasm defined as the proliferation of bone marrow langerhans cells, which is a kind of dendritic cells. the major pathological features of lch are expression of cd1a and s100 as well as birbeck granules. its presentation can differ from a mild bone lesion to a multi-systemic evolved malignant neoplasm; however, the latter outcome is almost rare. ...
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Langerhans cell histiocytosis (LCH) is a rare neoplasm defined as the proliferation of bone marrow langerhans cells, which is a kind of dendritic cells. The major pathological features of LCH are expression of CD1a and S100 as well as Birbeck granules. Its presentation can differ from a mild bone lesion to a multi-systemic evolved malignant neoplasm; however, the latter outcome is almost rare. ...
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عنوان ژورنال:
journal of research in medical sciencesجلد ۱۵، شماره ۱، صفحات ۵۸-۰
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