To clarify the role of concomitant carpal lesions in dislocated distal radius fractures (DRF), 104 consecutive patients with DRF underwent a preoperative morphological examination using CT and MRI. The study was performed between 2004 and 2006 with the aim of recording all types of concomitant carpal lesions as well as their consequences after 1 year. Carpal lesions of different types were found in all treated cases of dislocated DRF.
View Article and Find Full Text PDFIntroduction: Ligamentous lesions are concomitant to dislocated distal radius fractures in a high percentage. The purpose of this study was to evaluate the relevance of intracarpal lesions.
Methods: Seventy eight of an original cohort of 104 distal radius fractures (74%) were studied over a follow-up period of one year after surgery with complete data (X-rays, CT, MRI, follow-up X-rays and questionnaire).
Cystic formations around the knee are a common object of orthopedic treatment. When associated with neurological or vascular deficits further diagnostic imaging is required. This case study demonstrates the appearance of an intramuscular ganglion causing drop foot, arising from the tibio-fibular joint.
View Article and Find Full Text PDFBackground: Injuries due to domestic violence are a frequent occurrence in emergency departments. Although domestic violence has been well analyzed from the sociological point of view, medical data concerning patterns of injuries are rare.
Methods: Victims of domestic violence who presented at the emergency department of a maximum care hospital were included in the study.
Background: The functional outcome of surgically treated dislocated fractures of the distal radius is limited and does not correlate with radiographic results. Additional carpal lesions are assumed to be the cause. This study has evaluated which carpal lesions are associated with dislocated fractures of the distal radius.
View Article and Find Full Text PDFEur J Trauma Emerg Surg
December 2011
Introduction: Recent studies have raised the question of whether last year medical students and first year residents show an adequate attitude toward their patient's pain as reflected by prescribed pain medication. Underuse of analgetics could be demonstrated in several studies even after a correct diagnosis of pain was made and has led to the term "oligoanalgesia." Our study was aimed at evaluating the potential of improving student attitudes toward pain by changing the curriculum during the last year of medical education.
View Article and Find Full Text PDFPurpose: To present some retrospective data on the epidemiology of myelodysplastic syndrome (MDS) in Romania, in a large but well-defined territory and over a long period of time, as reflected by a large single-hospital based Registry.
Methods: The registration forms provided by the MDS Foundation were filled in with the data of the new adult primary MDS patients admitted in the Hematological Department of Fundeni Clinical Institute, Bucharest, during 1985-2004 and classified according to French-American-British (FAB) criteria.
Results: The study comprised 306 patients accrued from a delimited geo-administrative zone, 137 (45%) from Bucharest and 169 (55%) from the rest of the region.
In the Western countries the myelodysplastic syndrome (MDS) is mostly observed in patients older than 65 years and therefore there are few reports referring to patients less than 50 years. The aim of the study is to emphasize for the first time the characteristics of this group of age in Romania, a non-Western European country. The cases belonging to the group of age under 50 years were extracted from the database of the MDS Registry of the Hematological Department, Fundeni Clinical Institute, Bucharest, Romania, comprising 403 primary adult cases collected between 1982 and 2004.
View Article and Find Full Text PDFWe present the first Romanian study on the epidemiological characteristics of MDS, based on the data existing in Fundeni Clinical Institute, Hematological Department, Bucharest. The files at diagnosis of the adult patients with primary MDS admitted during the period 1982-2005, recorded in the registration forms provided by the MDS Foundation (USA), represented the primary database. This study indicates an increase in the number of new MDS cases over the period of time investigated.
View Article and Find Full Text PDFThe use of imatinib mesylate (IM) (Gleevec, Novartis) in chronic myeloid leukemia (CML) and other neoplastic disorders is in a dramatic increase, inducing long-standing survival. Therefore, the interest in the associated events with this treatment is more and more manifest. We describe a case of CML in which, at the usual antileukemic dose, IM induced a rapid and persistent normalization of the levels of serum cholesterol, triglycerides, low- and high-density lipoproteins and glucose.
View Article and Find Full Text PDFA 20 years old male patient was diagnosed as hypoplastic myelodysplastic syndrome (hMDS) - refractory cytopenia with multilineage dysplasia in November 2002. He received packed blood cells, methylprednisolon and dexamethason but no persistent improvement and even worsening of the thrombocytopenia and the appearance of neutropenia were registered. Laparoscopic splenectomy has been performed in January 2003, when the platelets were approximately 15000/mm3, without intraoperative incidents.
View Article and Find Full Text PDFChronic myelomonocytic leukemia (CMML) has long been recognized as a disorder with both myelodysplastic and myeloproliferative characteristics, some patients showing clinical and morphological features resembling myelodysplastic syndrome (MDS) especially refractory anemia with excess of blasts (RAEB) with monocytosis, and others leukocytosis with neutrophilia, monocytosis and splenomegaly resembling myeloproliferative syndrome (MPS). The intrinsec differences determined at first the separation of CMML in two forms, one named "dysplastic", more similar with RAEB, and the other "proliferative", closer to chronic myeloid leukemia and then included by the recent WHO classification into a separate new created group--myelodysplastic diseases (MDD)/chronic myeloproliferative diseases (CMPD). The aim of this study was the analysis of some features of 20 cases of CMML, with emphasis on the differences between the two forms.
View Article and Find Full Text PDFThe apparent contradiction between clonal expansion and marrow failure encountered in myelodysplastic syndromes (MDS) is more evident in hypocellular forms at presentation. Hypoplastic MDS (hMDS) appears to be a distinct clinicopathologic entity, accounting for about 15% from all MDS. The pathogeny is supposed to result from immunosupressive mechanisms and some observations on successful treatment with Cyclosporine A (CsA) are reported.
View Article and Find Full Text PDFBackground: Granulomas are encountered in 1-2% of biopsies performed in various hematological and non-hematological diseases. Almost 50% of bone marrow granulomas are associated with infections and 25% with hematologic disorders, especially lymphoma and multiple myeloma. Toxoplasmosis is reported to induce granulomas in bone marrow inmunosuppressed patients.
View Article and Find Full Text PDFThe paper presents a case of autoimmune hemolytic anemia (AIHA) with warm IgG antibodies associated with Waldenström's disease in which in the stage of compensated hemolysis after treatment, there appeared a severe hemolytic attack induced by transitory cold agglutinins with high thermal amplitude. The case described is a novelty by the intrication of two autoantibody populations which causes autoimmune hemolysis. The difference from other similar associations is discussed.
View Article and Find Full Text PDFRev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Med Interna
December 1988
Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Med Interna
August 1988
Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Med Interna
June 1982
Arch Roum Pathol Exp Microbiol
December 1989