منابع مشابه
Sweet syndrome in chronic myeloid leukaemia.
A 31-year-old woman with chronic myeloid leukemia developed bullous skin changes not responding to antibiotic therapy. A biopsy showed a sterile predominantly neutrophilic infiltrate consistent with Sweet's syndrome. These skin changes responded well to methylprednisolon. Seven months later the patient died in a blast crisis.
متن کامل'Lot's Wife' Syndrome in Acute Myeloid Leukaemia
Chronic hypodipsic hypernatraemia in the absence of clinical hypovolaemia, with normal renal function is rare, and has been reported principally in patients with known hypothalamic lesions.1'2 Hypernatraemia has been found in acute myeloid leukaemia, but only in association with diabetes insipidus.3 This appears to be the first reported case of chronic hypodipsic hypernatraemia complicating acu...
متن کاملHyponatraemia syndrome in acute myeloid leukaemia.
Hyponatraemia was observed in 11 out of 14 consecutive patients with acute myeloid leukaemia and its variants. Metabolic studies on these patients revealed an early increase in the urinary sodium excretion, negative free water clearance, and urine osmolality inappropriately higher than that of the serum. It is postulated that this syndrome is caused by a substance released from the primitive ce...
متن کاملGlutathione S-transferases Null Genotype in Acute Myeloid Leukaemia
Background: The glutathione S-transferase (GST) family of metabolising enzymes plays an important role in the detoxification of mutagens and carcinogens. The expression of many of these cancer susceptibility enzymes is genetically polymorphic. An increased frequency of GST-null genotypes has been associated with several malignancies. Objective: To investigate the rate of GSTT1 and GSTM1 null ge...
متن کاملCharacteristics of Sweet Syndrome in patients with acute myeloid leukemia.
INTRODUCTION Sweet syndrome (SS) is associated with hematologic malignancies including acute myeloid leukemia (AML). PATIENTS AND METHODS Records of patients with AML treated at our institution were reviewed to identify those with SS. Patient characteristics, laboratory values, and cytogenetic and molecular abnormalities were retrospectively reviewed. RESULTS We identified 21 of 2178 (1%) A...
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ژورنال
عنوان ژورنال: British Journal of Haematology
سال: 2019
ISSN: 0007-1048,1365-2141
DOI: 10.1111/bjh.15804