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  1. Article: Bizarre stromal cells in Crohn's disease.

    Iliakopoulos, Konstantinos / Tzikanoulas, Menelaos / Papaconstantinou, Ioannis / Tiniakos, Dina

    Annals of gastroenterology

    2019  Volume 32, Issue 3, Page(s) 312–315

    Abstract: Lesions with bizarre stromal cells (BSC) have been described in many organs and, although benign, they are frequently misdiagnosed as malignancy. We present the first case of BSC in Crohn's disease with a rare submucosal topography and we review the ... ...

    Abstract Lesions with bizarre stromal cells (BSC) have been described in many organs and, although benign, they are frequently misdiagnosed as malignancy. We present the first case of BSC in Crohn's disease with a rare submucosal topography and we review the related literature. We hypothesize that, in Crohn's disease, BSC of myofibroblastic origin may be related to the development of submucosal fibrosis.
    Language English
    Publishing date 2019-01-15
    Publishing country Greece
    Document type Case Reports
    ZDB-ID 2032850-3
    ISSN 1108-7471
    ISSN 1108-7471
    DOI 10.20524/aog.2019.0347
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 2455: Show issues Location:
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    ab Jg. 2022: Lesesaal (EG)

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  2. Article: Primary adrenal leiomyosarcoma: A case report.

    Sakellariou, Maria / Dellaportas, Dionysios / Grapsa, Eirini / Tzikanoulas, Menelaos / Dellis, Athanasios / Theodosopoulos, Theodosios / Nastos, Constantinos

    Molecular and clinical oncology

    2020  Volume 12, Issue 4, Page(s) 317–320

    Abstract: Adrenal leiomyosarcomas are rare mesenchymal tumors of the suprarenal region that are usually diagnosed after they have reached a large size. We report the case of a 62-year-old male with an incidentally found left adrenal mass. Magnetic resonance ... ...

    Abstract Adrenal leiomyosarcomas are rare mesenchymal tumors of the suprarenal region that are usually diagnosed after they have reached a large size. We report the case of a 62-year-old male with an incidentally found left adrenal mass. Magnetic resonance imaging of the retroperitoneal space showed a heterogeneously enhanced mass, measuring 10x8.2 cm, with characteristics suspicious of malignancy. The patient underwent left radical adrenalectomy after the hormonal evaluation of the tumor due to the high probability of adrenocortical carcinoma. However, microscopic examination of the tumor showed a spindle cell sarcoma. Immunohistochemically the neoplastic cells were found positive for desmin and smooth muscle actin and the diagnosis of a well differentiated adrenal leiomyosarcoma was established. During follow-up the patient presented an aggressive course as he developed bone, liver and pulmonary metastases early postoperatively, which were treated with radiation therapy and chemotherapy. The patient has progressive metastatic disease while on chemotherapy 31 months after surgery.
    Language English
    Publishing date 2020-01-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 2796865-0
    ISSN 2049-9469 ; 2049-9450
    ISSN (online) 2049-9469
    ISSN 2049-9450
    DOI 10.3892/mco.2020.1987
    Database MEDical Literature Analysis and Retrieval System OnLINE

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