Calcinosis cutis: a rare complication of chronic myeloid leukemia
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چکیده
منابع مشابه
Calcinosis Cutis: A Rare Complication Following Liver Transplantation
The clinical manifestations of calcinosis cutis vary from asymptomatic cutaneous papules to lifethreatening calciphylaxis. We describe a 61-year-old female who was found to have extensive calcinosis cutis on her left forearm 4 days following liver transplantation. Large amount of calcium chloride solution was intravenously infused during the operation at the same site without gross extravasatio...
متن کاملIatrogenic calcinosis cutis: A rare cytological diagnosis
Calcinosis cutis is an uncommon condition characterized by the deposition of calcium salts in the subcutaneous tissues of the body. Calcifications can also occur in a variety of other clinical settings and can be subjected to fine-needle aspiration (FNA). Since cutaneous calcific deposits may clinically mimic a tumor, it is feasible to diagnose them by FNA cytology (FNAC). We reported a case of...
متن کاملA Rare Case of Acute Myeloid Leukemia with Translocation (3:3) Presenting with Features of Chronic Myelomonocytic Leukemia
Background: Acute Myeloid Leukemia (AML) with translocation (3,3) is a form of AML that may present de novo or may arise from a previous myelodysplastic syndrome. It is often associated with normal or elevated peripheral blood platelet count and increased bone marrow megakaryocytes with associated multi lineage dysplasia. A subset of patients present with hepatosplenomegaly while a few cases h...
متن کاملCalcinosis cutis.
1 of 2 DESCRIPTION An 87-year-old woman with a history of hypertension, atrial fi brillation, and mixed connective tissue disease was admitted to hospital because of heart failure. Besides clinical signs of ventricular dysfunction, physical examination showed painless, subcutaneous nodules that had developed during the past 10 years on her left elbow ( fi gure 1A ) and knees ( fi gure 1B , righ...
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ژورنال
عنوان ژورنال: Annals of Saudi Medicine
سال: 2006
ISSN: 0256-4947,0975-4466
DOI: 10.5144/0256-4947.2006.62