3,590 research outputs found

    Galactic center GeV gamma-ray excess from dark matter with gauged lepton numbers

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    The recently observed excess in gamma-ray signal near the Galactic center suggests that dark matter particles may annihilate into charged fermions that produce gamma-ray to be observed. In this paper, we consider a leptonic dark matter, which annihilates into the standard model leptons, μ+μ\mu^+ \mu^- and τ+τ\tau^+ \tau^-, by the interaction of the gauged lepton number U(1)LμLτ{\rm U(1)}_{L_\mu-L_\tau} and fits the observed excess. Interestingly, the necessary annihilation cross section for the observed gamma-ray flux provides a good fit to the value for the relic abundance of dark matter. We identify the preferred parameter space of the model after taking the existing experimental constraints from the precision measurements including the muon (g2)(g-2), tau decay, neutrino trident production, dark matter direct detection, LHC, and LEP experiments.Comment: 18 pages, 8 figures, references added, matches published versio

    511 keV γ\gamma-ray emission from the galactic bulge by MeV millicharged dark matter

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    We propose a possible explanation for the recently observed anomalous 511 keV line with a new "millicharged" fermion. This new fermion is light [O(MeV){\cal O}({\rm MeV})]. Nevertheless, it has never been observed by any collider experiments by virtue of its tiny electromagnetic charge ϵe\epsilon e. In particular, we constrain parameters of this millicharged particle if the 511 keV cosmic γ\gamma-ray emission from the galactic bulge is due to positron production from this new particle.Comment: 3 pages, 1 figure, A talk given by J.C.Park at the 16th International Conference on Supersymmetry and the Unification of Fundamental Interactions (SUSY08), Seoul, Korea, June 16-21, 200

    Primary renal well-differentiated neuroendocrine tumors: report of six cases with an emphasis on the Ki-67 index and mitosis

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    Background Primary renal well-differentiated neuroendocrine tumors (WDNETs) also called carcinoid and atypical carcinoid are extremely rare, and little is known about parameters that may predict prognosis at diagnosis. Methods Six cases of primary renal WDNET were collected. After reviewing slides stained with hematoxylin and eosin, proportions of each growth pattern were determined. Synaptophysin, chromogranin, CD56, and Ki-67 immunostaining and Ki-67 morphometric analysis were performed. Results Patients included three female and three males, mean age was 53.3 years. The mean tumor size was 4.5 cm, three cases were greater than 5 cm. At the time of initial surgery, lymph node and/or distant metastasis was confirmed in two cases. In a third case, no metastasis was initially found, but lymph node metastasis was identified during follow-up. The remaining three cases did not exhibit metastasis. Histopathologically, the renal WDNETs were primarily composed of ribbon-like and sheet-like growth patterns. Most of the tumors were diffusely positive for neuroendocrine markers. Mitotic count was high (≥2/10HPF) in cases with lymph node or distant metastasis but was low (< 2/10HPF) in non-metastatic cases. Furthermore, the Ki-67 index was also higher (≥3%) in the cases with metastases than in cases without metastasis. Conclusion Three out of the six primary renal WDNETs demonstrated aggressive behavior and exhibited increased mitotic counts and Ki-67 indices. These results suggest that mitosis and the Ki-67 index could be used as prognostic indicators for renal WDNET.This work was supported by grant 04–2016-0460 from the Seoul National University Hospital Research Fund
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