Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Zoi A. Tatsiou"'
Publikováno v:
Chirurgische Gastroenterologie. 24:171-174
Background: In the absence of any initial hematological abnormality, the diagnosis of myeloid sarcoma (MS) is very difficult. A review of the literature revealed that only 15 cases
Publikováno v:
Leukemia & Lymphoma. 46:451-455
Non-Hodgkin's lymphoma (NHL) of the breast may be primary or secondary. Both are rare and there are no morphological criteria to make the differential diagnosis. Benign intramammary lymph nodes are often encountered, but the development of either pri
Publikováno v:
Onkologie. 32(6)
Background: Mature cystic teratoma, also known as dermoid cyst, is the most common germ cell tumor of the ovary. Malignant change in a component of a mature ovarian teratoma is rare, occurring in less than 2% of cases, with squamous cell carcinoma co
Publikováno v:
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases. 13(4)
Summary Visceral leishmaniasis (VL) is a relatively rare occurrence in rheumatoid arthritis (RA) patients treated with tumor necrosis factor-α (TNF-α) antagonists, corticosteroids and methotrexate, or methotrexate alone. A review of the literature
Publikováno v:
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery. 265(6)
Kaposi's sarcoma (KS) is an unusual vascular tumor characterized by multiple reddish blue nodules, which usually present on the skin of the lower and upper extremities. KS may also involve mucosal sites, lymph nodes and visceral organs. During the la
Publikováno v:
International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists. 25(1)
Langerhans cell histiocytosis (LCH) of the female genital tract is very rare. A review of the literature revealed that only 12 cases of primary vulvar LCH have previously been published. We describe an additional case of LCH in which the disease was
Autor:
Jörg Kleeff, Alexandra Westerholt, Bo Chen, Anne Glitsch, Hodjat Shekarriz, Helmut Friess, Thomas Karger, Ayşse Bilgihan, Matthias Kraft, Hualong Yu, André L. Mihaljevic, A. Kutup, Peter Kujath, Stefan A. Maier, Norbert Senninger, Lerch Nil, Ulrike Seltrecht, Maciej Patrzyk, H. Naumann, I. Partecke, Bülent Ünal, H. Hartmann, Ali A. Aghdassi, Claus-Dieter Heidecke, Wenbin Yu, Hüseyin Üstün, Markus M. Lerch, Hartmut Paul, Jianing Liu, Thomas Vogel, Jörg Ringel, Ş. Melih Karabeyoğlu, A. Schreiber, Fatma Öz Atasay, Bernhard Henning, Osman Cem Yilmaz, Bo Li, Wolfram von Bernstorff, Holger Bartels, Marc Nocon, Jens Brockmann, Omer Cengiz, E.F. Yekebas, Jens Hartmann, Uwe Bergmann, Ioannis Goulis, Ioannis D. Venizelos, Fengchun Wang, Martin Hoffmann, Christoph A. Jacobi, Sanyuan Hu, Julia Mayerle, Jürgen Ordemann, Zoi A. Tatsiou, Peter Simon, Betül Bozkurt, Andreas Sendler, Stephan Jonas, J.R. Izbicki, Ulrich Wahnschaffe, George Frakandreas
Publikováno v:
Chirurgische Gastroenterologie. 24:154-155