Subject(s)
Dermatomyositis/diagnosis , Liver Neoplasms/diagnosis , Lymphoma/diagnosis , Paraneoplastic Syndromes/diagnosis , Dermatomyositis/etiology , Dermatomyositis/pathology , Female , Humans , Liver Neoplasms/complications , Liver Neoplasms/pathology , Lymphoma/complications , Lymphoma/pathology , Middle Aged , Paraneoplastic Syndromes/etiology , Paraneoplastic Syndromes/pathologyABSTRACT
PURPOSE OF THE STUDY: Deep vein thrombosis is a common condition in geriatric. The identification of risk factors for venous thrombosis in the elderly is important because it allows an appropriate prescription of preventive treatments. The purpose of this study is to identify the etiologic and therapeutic characteristics of deep vein thrombosis of the lower limbs in the elderly. PATIENTS AND METHODS: A retrospective study of 155 patients with lower limb deep vein thrombosis confirmed by venous Doppler. These patients were divided into two groups: group 1 (patients aged 65 years or more) and group 2 (patients whose age was below 65 years). A comparison between these two groups was performed. RESULTS: The average age of patients in group 1 was 74.89 years (± 6.43). The sex ratio in this group was 0.68. The thrombosis was more frequently proximal in patients of group 1. Patients of group 1 had significantly more risk factors than those of group 2 (p <0.05). Among risk factors studied, only the cancers were significantly more frequent in group 1 (p = 0.002). The frequency of hemorrhagic events in both groups was comparable but bleeding was more common in patients of group 1 with cancer. CONCLUSION: Our study confirms the multifactorial origin of deep vein thrombosis in the elderly and the incidence of malignant etiology. The results of this study also call for vigilance in the use of anticoagulants in the elderly especially in the presence of cancer because it is an additional risk factor for bleeding.
ABSTRACT
BACKGROUND: Hemophagocytic syndromes are mostly associated with underlying pathology, they can reveal: immunodeficiency, infections, hemopathies, cancers and auto-immune diseases. AIM: to investigate clinical, biological features, outcome characteristics and underlying pathology of Tunisian patients with hemophagocytic syndromes. METHODS: A retrospective study of patients with hemophagocytic syndromes admitted in an internal medicine department in Tunis over the period 2009-2012. RESULTS: There were 11 patients included, 4 men and and 7 women. Mean age was 47,3years. Purpura was observed in 3 cases, hepatosplenomegaly in 6 cases and peripheral lymph nodes in 3 cases. Hemorrhagic complication was noted in 2 cases. There were an increase of inflammatory indices in all the cases. Eight patients had pancytopenia and 3 had bicytopenia. Six patients developed intravascular dissiminated coagulation. High levels of triglyceridemia was noted in 5 cases and an hyperferritinaemia in all cases. Cytological examination of bone marrow confirmed hemophagocytosis in ten cases. Hemophagocytosis was associated to infectious diseases in 6 cases, there were 2 cases of leishmaniasis, septicemia to E.Coli and staphylococcus aureus and lymph nodes tuberculosis with HIV. We also noted a case of lymphoma, myelodysplasic syndrome, rheumatoid polyarthritis, adult onset still's disease. In one patient, the origin of hemophagocytosis remained indefinite. Visceral leishmaniose were treated by Glucantime®, adult Still's disease by corticosteroids and méthrotrexate®, lymphoma by chemotherapy. In lymph nodes tuberculosis, there were good evolution. Six patients died. CONCLUSION: Hemophagocytic syndrome is a rare and life-threatening disease. Pejorative prognosis requires an early therapy with etiological treatment.
Subject(s)
Macrophage Activation Syndrome , Adolescent , Adult , Aged , Female , Hepatomegaly/diagnosis , Hepatomegaly/epidemiology , Hepatomegaly/etiology , Humans , Macrophage Activation Syndrome/diagnosis , Macrophage Activation Syndrome/epidemiology , Macrophage Activation Syndrome/etiology , Male , Middle Aged , Prognosis , Retrospective Studies , Splenomegaly/diagnosis , Splenomegaly/epidemiology , Splenomegaly/etiology , Tunisia/epidemiology , Young AdultSubject(s)
Hypereosinophilic Syndrome/complications , Hypereosinophilic Syndrome/diagnosis , Raynaud Disease/complications , Adult , Angiography , Diagnosis, Differential , Fingers/blood supply , Fingers/diagnostic imaging , Humans , Leg/blood supply , Leg/diagnostic imaging , Male , Raynaud Disease/diagnosisABSTRACT
Leukemoid reaction is a rare paraneoplastic syndrome. It can occur in association with carcinomas, in particular of the lung, gastric and renal. However, its association with sarcoma is infrequent. Leukemoid reaction occuring in patients with uterine sarcoma have not been previously reported. We report the case of a « leukemoid ¼ leucocytosis revealing an uterine sarcoma with fatal evolution.
Subject(s)
Leukemoid Reaction/diagnosis , Leukocytosis/diagnosis , Fatal Outcome , Female , Humans , Leukemoid Reaction/complications , Leukocytosis/complications , Middle Aged , Sarcoma/complications , Sarcoma/diagnosis , Uterine Neoplasms/complications , Uterine Neoplasms/diagnosisABSTRACT
BACKGROUND: Disseminated intravascular coagulation (DIC) is a severe disease. It can be caused by loss of pathology. CASE REPORT: We report the case of chronic aortic dissection discovered during the evaluation of disseminated intravascular coagulation (DIC). This case is characterised by the severity of clinical presentation, challenging diagnosis and difficulty of therapeutic approach. Low dose of heparine may reduce the severity of this situation; but vital prognosis remains obscure. CONCLUSION: aortic dissection is a rare but a severe cause of disseminated intravascular coagulation
