Pulmonary Langerhans Cell Histiocytosis in pre-existing chronic myelomonocytic leukaemia: a rare association.
نویسندگان
چکیده
Pulmonary Langerhans Cell Histiocytosis in pre-existing chronic myelomonocytic leukaemia: a rare association J. Temporal, L. Armstrong, N. Bhatt and A.R.L. Medford From the North Bristol Lung Centre, Southmead Hospital, Westbury-on-Trym, Bristol BS10 5NB, England, UK, Department of Radiology, Southmead Hospital, Westbury-on-Trym, Bristol BS10 5NB, England, UK and Department of Pathology, Bristol Royal Infirmary, Bristol BS2 8HW, England, UK
منابع مشابه
Letterer-Siwe disease associated with chronic myelomyonocytic leukemia: a fortuitous association?
Langerhans cell histiocytosis (LCH) and malignancy occurring in the same individual is unusual and has generally been the subject of isolated case reports. LCH is a rare condition in adults. Its cause is uncertain but, with the recent demonstration of clonality and its association with malignant disease, there has been a renewal of interest. We report a singular case of Letterer-Siwe disease as...
متن کاملLangerhans Cell Histiocytosis in Childhood: Review, Symptoms in the Oral Cavity, Differential Diagnosis and Report of One Case
Background Langerhans cell histiocytosis (LCH) is a rare disease in which monoclonal migration and proliferation of specific dendritic cells is seen. The disease primarily affects the bones and skin, but there is a possibility that involves other organs or appears as a multi-systemic disease. Case Report In oral examination of a nine-month girl, two deep wounds with a yellow membrane with appro...
متن کاملگزارش یک مورد Langerhans cell histiocytosis در یک کودک 3 ساله با تظاهرات اولیه دهانی
Langerhans cell histiocytosis (LCH) is a rare disease with formation of granulomatous infiltrations consisting of Langerhans cells, histiocytes, lymphocytes and eosinophilic granulocytes. The ethiopathogenesis of the disease has not been fully clarified yet. It can occur as focal or disseminated form - acute or chronic. Oral manifestations may be the first signs. This article reports a case of ...
متن کاملIndeterminate cell histiocytosis: a case report
Indeterminate cell histiocytosis is a very rare proliferative disorderof histiocytes which displays both langerhans cell histiocytosisand non langerhans cell histiocytosis immunophenotypic features.The majority of the patients develop multiple lesions which areclinically indistinguishable from generalized eruptive histiocytosis.We report a 14-year-old girl with multiple papules on the face,scal...
متن کاملHairy cell leukaemia.
Hairy cell leukaemia is a rare form of lymphoproliferative disease that affects 2% of leukaemia patients and was first described in 1958 as leukaemic reticuloendotheliosis. The typical presentation is pancytopenia, splenomegaly and abnormal lymphoid cells in blood with hairy cytoplasmic projections. The pathological hairy cell resembles in many ways B-lymphocyte as in chronic lymphocytic leukae...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- QJM : monthly journal of the Association of Physicians
دوره 109 3 شماره
صفحات -
تاریخ انتشار 2016