Thymoma-associated Graft-versus-Host Disease-like Erythroderma

We report a 40-year-old woman with recurrent thymoma associated with myasthenia gravis, in whom an unusual form of erythroderma developed. A histological examination revealed a graft-versus-host disease (GVHD)-like reaction. After high-dose steroid therapy, the metastatic thymoma lesion in the abdominal cavity was reduced in size from 9.5 × 6 × 7.5 cm to 4 × 3 × 1 cm in diameter. Nevertheless, the GVHD-like erythroderma become aggravated, her condition worsened, and the patient finally suffered from respiratory failure and died of sepsis. A GVHD-like reaction may be a rare presentation of thymoma-associated immunological disorders such as myasthenia gravis or pure red cell aplasia. Herein, we discuss the present case and review pertinent reports of thymoma cases associated with GVHD

Clarifying the Destructive Influence of Gravitation Set in Infusion Pump

Import 22/07/2015Infuzní léčba je v současnosti jedním z nejběžnějších úkonů, prováděných ve zdravotnických zařízeních, a nachází uplatnění v širokém spektru případů. Samotný proces léčby může být uskutečněn dvěma způsoby – gravitační infuzí a použitím volumetrické infuzní pumpy. Princip infuze řízené volumetrickou pumpou klade specifické nároky na vlastnosti užívaných infuzních setů, přičemž pro zajištění důležité přesnosti průtoku je nezbytné dbát na určení daného setu pro použití s tlakovou metodou. V běžném zdravotnickém prostředí však existuje řada rizikových faktorů, jejichž vlivem může dojít k porušení této podmínky kompatibility a následnému použití volumetrické pumpy s nevhodnou administrativní soupravou, určenou pouze pro gravitační infuzi. Záměrem první části této práce je, na základě známých poznatků o negativních vlivech činnosti pumpy na přesnost léčby a o mechanických vlastnostech infuzních setů, teoreticky stanovit možné destrukční vlivy čerpadla infuzní pumpy na materiál gravitačního setu. Cílem druhé části je pokusit se prokázat negativní dopad mechanického namáhání gravitačního setu v infuzní pumpě na přesnost dávkování a vlastnosti materiálu použitého setu pomocí experimentálně získaných dat.Intravenous therapy is currently one of the most common operations performed in health care facilities, finding its use in a wide range of cases. The particular process of treatment can be implemented in two ways - using gravity-fed infusion and by use of volumetric infusion pump. The principle of infusion controlled by a volumetric pump lays specific demands on the quality of the infusion sets in use. When warranting the flow rate accuracy it is necessary to ensure suitability of the set for use with the pressure method. However, there are a number of risk factors in common medical situations, whose influence may lead to violating the terms of compatibility and the subsequent use of a volumetric pump with an improper administrative set made only for gravity-fed infusion. The aim of the first part of this work is the theoretical determination of the possible destructive effects of the infusion pump to the material of a gravity-fed administration set based on the evidence about the negative impacts of the pump on the flow rate accuracy and mechanical characteristics of the infusion sets. The goal of the second part is an effort to proof the negative impact of the mechanical stress of a gravity set in an infusion pump to dosage accuracy and the material properties of the used set through experimental data.450 - Katedra kybernetiky a biomedicínského inženýrstvívýborn

Malignant and Benign T Cells Constituting Cutaneous T-Cell Lymphoma

Cutaneous T-cell lymphoma (CTCL) is a heterogeneous group of non-Hodgkin lymphoma, including various clinical manifestations, such as mycosis fungoides (MF) and Sézary syndrome (SS). CTCL mostly develops from CD4 T cells with the skin-tropic memory phenotype. Malignant T cells in MF lesions show the phenotype of skin resident memory T cells (TRM), which reside in the peripheral tissues for long periods and do not recirculate. On the other hand, malignant T cells in SS represent the phenotype of central memory T cells (TCM), which are characterized by recirculation to and from the blood and lymphoid tissues. The kinetics and the functional characteristics of malignant cells in CTCL are still unclear due, in part, to the fact that both the malignant cells and the T cells exerting anti-tumor activity possess the same characteristics as T cells. Capturing the features of both the malignant and the benign T cells is necessary for understanding the pathogenesis of CTCL and would lead to new therapeutic strategies specifically targeting the skin malignant T cells or benign T cells

c-FOS Expression in Metastatic Basal Cell Carcinoma with Spontaneous Basosquamous Transition

Abstract is missing (Short communication

A rare case of folliculotropic mycosis fungoides with eosinophilic pneumonia

We describe the first case of folliculotropic mycosis fungoides (FMF) involving eosinophilic pneumonia (EP). It would be difficult to treat EP without CTCL treatment

P-REX1 amplification promotes progression of cutaneous melanoma via the PAK1/P38/MMP-2 pathway.

P-REX1 (PIP3-dependent Rac exchange factor-1) is a guanine nucleotide exchange factor that activates Rac by catalyzing exchange of GDP for GTP bound to Rac. Aberrant up-regulation of P-REX1 expression has a role in metastasis however, copy number (CN) and function of P-REX1 in cutaneous melanoma are unclear. To explore the role of P-REX1 in melanoma, SNP 6.0 and Exon 1.0 ST microarrays were assessed. There was a higher CN (2.82-fold change) of P-REX1 in melanoma cells than in melanocytes, and P-REX1 expression was significantly correlated with P-REX1 CN. When P-REX1 was knocked down in cells by P-REX1 shRNA, proliferation, colony formation, 3D matrigel growth, and migration/invasiveness were inhibited. Loss of P-REX1 inhibited cell proliferation by inhibiting cyclin D1, blocking cell cycle, and increased cell apoptosis by reducing expression of the protein survivin. Knockdown of P-REX1 expression inhibited cell migration/invasiveness by disrupting P-REX1/RAC1/PAK1/p38/MMP-2 pathway. Assessment of patient tumors and disease outcome demonstrated lower distant metastasis-free survival among AJCC stage I/II/III patients with high P-REX1 expression compared to patients with low P-REX1 expression. These results suggest P-REX1 plays an important role in tumor progression and a potential theranostic target

Kososan, a Kampo medicine, prevents a social avoidance behavior and attenuates neuroinflammation in socially defeated mice

Abstract Background Kososan, a Kampo (traditional Japanese herbal) medicine, has been used for the therapy of depressive mood in humans. However, evidence for the antidepressant efficacy of kososan and potential mechanisms are lacking. Recently, it has been recognized that stress triggers neuroinflammation and suppresses adult neurogenesis, leading to depression and anxiety. Here, we examined whether kososan extract affected social behavior in mice exposed to chronic social defeat stress (CSDS), an animal model of prolonged psychosocial stress, and neuroinflammation induced by CSDS. Methods In the CSDS paradigm, C57BL/6J mice were exposed to 10 min of social defeat stress from an aggressive CD-1 mouse for 10 consecutive days (days 1–10). Kososan extract (1.0 g/kg) was administered orally once daily for 12 days (days 1–12). On day 11, the social avoidance test was performed to examine depressive- and anxious-like behaviors. To characterize the impacts of kososan on neuroinflammation and adult neurogenesis, immunochemical analyses and ex vivo microglial stimulation assay with lipopolysaccharide (LPS) were performed on days 13–15. Results Oral administration of kososan extract alleviated social avoidance, depression- and anxiety-like behaviors, caused by CSDS exposure. CSDS exposure resulted in neuroinflammation, as indicated by the increased accumulation of microglia, the resident immune cells of the brain, and their activation in the hippocampus, which was reversed to normal levels by treatment with kososan extract. Additionally, in ex vivo studies, CSDS exposure potentiated the microglial pro-inflammatory response to a subsequent LPS challenge, an effect that was also blunted by kososan extract treatment. Indeed, the modulatory effect of kososan extract on neuroinflammation appears to be due to a hippocampal increase in an anti-inflammatory phenotype of microglia while sparing an increased pro-inflammatory phenotype of microglia caused by CSDS. Moreover, reduced adult hippocampal neurogenesis in defeated mice was recovered by kososan extract treatment. Conclusions Our findings suggest that kososan extract prevents a social avoidant behavior in socially defeated mice that is partially mediated by the downregulation of hippocampal neuroinflammation, presumably by the relative increased anti-inflammatory microglia and regulation of adult hippocampal neurogenesis. Our present study also provides novel evidence for the beneficial effects of kososan on depression/anxiety and the possible underlying mechanisms