Osteitis Fibrosa Quística y Síndrome Hipercalcemico como Manifestación inicial de Leucemia Linfoblástica
نویسندگان
چکیده
منابع مشابه
Not too much hyperextension: airway positioning using magnetic resonance imaging.
trombocitopenia, característica del HELLP, con la aparición de hipopituitarismo2. La clínica puede aparecer de meses a años tras la agresión inicial; destacan: astenia, amenorrea, agalactia, hipoglucemia, hipotensión, intolerancia al frío y pérdida de vello púbico y axilar1,3. La cirugía, los traumatismos o las infecciones pueden precipitar o agravar los síntomas, favoreciendo la aparición de s...
متن کاملOsteitis Fibrosa Cystica Mistaken for Malignant Disease
A 65-year-old man with back pain had plain radiographs that showed multiple osteolytic bone lesions of the pelvis, femur and L-spine; an magnetic resonance imaging scan of the L-spine showed extensive bony resorption with a posterior epidural mass involving the L1 spinous process; these findings suggested multiple myeloma or bony metastasis. However, all serology testing was negative. The parat...
متن کاملGeneralized Osteitis Fibrosa with Parathyroid Adenoma
or disseminated sclerosis but I was told that she had had some pain around the groin, that her doctor had sent her for X-ray of the pelvis, and that a large destructive lesion had been found in one of the pubic rami. A surgeon saw her and advised that she should be admitted to a chronic hospital: the diagnosis was secondary tumours of bone. When I first looked at this X-ray picture of the pubis...
متن کاملNormacalcaemic primary hyperparathyroidism with osteitis fibrosa.
THE diagnosis of primary hyperparathyroidism has been classically based upon the demonstration of high plasma calcium and low plasma phosphorus concentrations and an excessive urinary excretion of calcium. In recent years, however, it has become recognized that patients with primary hyperparathyroidism may present with plasma calcium concentrations that are within the normal range (George et al...
متن کاملMacrophage Activation Syndrome as the Initial Manifestation of Severe Juvenile Onset Systemic Lupus Erythematosus. Favorable Response to Cyclophosphamide
The macrophage activation syndrome is a rare but potentially fatal complication of patients with autoimmune rheumatic diseases. This is a clinicopathological entity characterized by activation of histiocytes with prominent hemophagocytosis in the bone marrow and other reticuloendothelial systems. In patients with lupus it may mimic an exacerbation of the disease or infection. We report the case...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Revista chilena de pediatría
سال: 1985
ISSN: 0370-4106
DOI: 10.4067/s0370-41061985000300008