Alien vascular plants in the Silesian Upland of Poland: distribution, patterns, impacts and threats

Symptoms of anthropogenic changes in the flora include processes of extinction in some species and spread in others. These tendencies have increased in magnitude in recent centuries, adversely affecting natural biodiversity on a regional, national and continental scale. The main idea behind the project presented here was to investigate the diversity of the alien vascular flora at the regional scale and to update the list of invasive alien species for the Silesian Upland. The aim of this study is also to provide a synthesis of the knowledge accumulated to date on the conditions for their occurrence, their distribution patterns and the possible threat they might pose. The distribution of particular species at the regional scale was investigated by mapping the species on a 2 km x 2 km grid. The study showed that the list of alien plant species for the Silesian Upland encompasses 338 species, including 125 archaeophytes, 195 kenophytes (=neophytes) and 18 species of an uncertain status in the Polish flora. A threat evaluation was performed for particular species on the basis of the number of localities, the diversity of preferred habitats recorded, and their current (over the last decade) tendency to colonise new localities. As a result, a final list of 101 invasive species has been selected. Among the alien plant species considered to be invasive in the area of the Silesian Upland, 20 species are identified as Çweedsí (13 archaeophytes and 7 kenophytes), another 25 (exclusively kenophytes), penetrating into natural habitats, are defined as Çtransformersí

Trudne, bo nietypowe przypadki guzów litych u dzieci

Nietypowy obraz kliniczny nowotworów wieku dziecięcego niejednokrotnie stwarza trudności diagnostyczne i staje się przyczyną opóźnień w ustaleniu rozpoznania. Poniżej przedstawiamy troje dzieci z rozpoznaniami guzów litych o nietypowym przebiegu klinicznym, leczonych w Klinice Pediatrii, Hematologii, Onkologii i Endokrynologii Akademii Medycznej w Gdańsku

Childhood rhabdomyosarcoma metastatic to bone marrow presenting with disseminated intravascular coagulation and acute tumour lysis syndrome: review of the literature apropos of two cases

The paper presents diagnostic and therapeutic difficulties in two adolescents with widespread rhabdomyosarcoma (RMS) presenting with severe haemorrhages resulting from disseminated intravascular coagulation (DIC) and with laboratory features of acute tumour lysis syndrome (ATLS). Other published cases of childhood RMS with DIC at admission have been listed and reviewed. It has been concluded that the clinical picture of a widespread RMS in children may resemble acute hematologic malignancy and pose a big diagnostic problem. That is why the presence of small blue round cells morphologically similar to lymphoblasts and/or myeloblasts in bone marrow (BM), lacking hematopoietic makers, should prompt the pathologist to consider possible diagnosis of RMS. Inclusion of desmin, MyoD1 and myogenin Myf4 to the immunohistochemical panel is obligatory in such cases. When the representative histopathological tumour specimens are difficult to obtain, the flow cytometric immunophenotyping of BM metastases could help the standard morphological/immunohistological diagnostic procedures and advance the diagnosis. Recently, the flow cytometric CD45− CD56+ immunophenotype together with Myf4 transcript has been assigned to RMS cells infiltrating BM. In children with disseminated RMS complicated with DIC rapid polychemotherapy aimed at diminishing the malignancy-triggered procoagulant activity should be initiated. However, in cases with concomitant ATLS the initial doses of chemotherapy should be reduced and the metabolic disorders and renal function monitored. The prognosis in children with RMS metastatic to BM with signs of DIC or ATLS at admission depends on the response to chemotherapy, however generally it is highly disappointing