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  1. Artikel: Persistent Hepatitis E Infection in a Patient with Tuberous Sclerosis Complex Treated with Everolimus: A Case Report.

    van Dijk, Wobke E M / Vergeer, Menno A M H / Arends, Joop E

    Infectious diseases and therapy

    2017  Band 6, Heft 2, Seite(n) 291–295

    Abstract: Introduction: The incidence of hepatitis E (HEV) genotype 3 is rising in developed countries. HEV infections are usually self-limiting, but can become chronic in immunocompromised patients. This might lead to rapid fibrosis development even resulting in ...

    Abstract Introduction: The incidence of hepatitis E (HEV) genotype 3 is rising in developed countries. HEV infections are usually self-limiting, but can become chronic in immunocompromised patients. This might lead to rapid fibrosis development even resulting in cirrhosis. Chronic HEV is mainly described in patients after solid-organ or hematological transplantations. We present the first case of HEV infection in a patient with tuberous sclerosis complex (TSC) treated with everolimus, a mammalian target of rapamycin (mTOR) inhibitor.
    Case: A 46-year-old male with TSC was referred to the infectious diseases department with an acute rise of liver enzymes during routine laboratory check-up. He was diagnosed with an acute HEV infection. His current treatment for TSC was everolimus. After awaiting a spontaneous clearance for 3 months, everolimus was discontinued. Hereafter, the infection was cleared within another 3 months.
    Discussion: Due to a favorable side-effect profile, everolimus is gaining popularity as an immunosuppressive therapy. However, in vitro experiments suggest that inhibition of mTOR leads to a significant increase in HEV replication. Thus far, there have been no clinical reports of HEV infections in patients treated with everolimus.
    Conclusion: Due to higher dosing of everolimus in TSC patients, they are more vulnerable to the development of chronic HEV infection. Periodic assessment of transaminases in these patients is advised.
    Sprache Englisch
    Erscheinungsdatum 2017-03-03
    Erscheinungsland New Zealand
    Dokumenttyp Journal Article
    ZDB-ID 2701611-0
    ISSN 2193-6382 ; 2193-8229
    ISSN (online) 2193-6382
    ISSN 2193-8229
    DOI 10.1007/s40121-017-0147-0
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Risk of breast cancer in patients with lymphangioleiomyomatosis.

    Nuñez, Olivier / Baldi, Bruno G / Radzikowska, Elżbieta / Carvalho, Carlos R R / Herranz, Carmen / Sobiecka, Malgorzata / Torre, Olga / Harari, Sergio / Vergeer, Menno A M H / Kolbe, John / Pollán, Marina / Pujana, Miquel Angel

    Cancer epidemiology

    2019  Band 61, Seite(n) 154–156

    Abstract: Lymphangioleiomyomatosis (LAM) is a rare metastasizing pulmonary disease that shares some clinical, cellular, and molecular similarities with metastatic breast cancer to lung. LAM cells have been identified circulating in various body fluids of patients ... ...

    Abstract Lymphangioleiomyomatosis (LAM) is a rare metastasizing pulmonary disease that shares some clinical, cellular, and molecular similarities with metastatic breast cancer to lung. LAM cells have been identified circulating in various body fluids of patients and, intriguingly, diverse evidence indicates that these cells may originate from a different organ to the lung. Following on from these observations, we hypothesized the existence of a common risk basis between LAM and breast cancer, and suggested increased risk of breast cancer among LAM patients. Here, by studying two additional LAM cohorts with more detailed epidemiological, life-style, and disease-related data, we show consistent results; a potential excess of estrogen-receptor-positive young breast cancer cases in LAM. This observation further suggests the need of prospective studies to precisely assess the association between both diseases.
    Mesh-Begriff(e) Breast Neoplasms/etiology ; Breast Neoplasms/pathology ; Female ; Humans ; Lymphangioleiomyomatosis/complications ; Lymphangioleiomyomatosis/pathology ; Neoplasm Metastasis ; Prospective Studies
    Sprache Englisch
    Erscheinungsdatum 2019-06-28
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2508729-0
    ISSN 1877-783X ; 1877-7821
    ISSN (online) 1877-783X
    ISSN 1877-7821
    DOI 10.1016/j.canep.2019.06.004
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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