LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 3 of total 3

Search options

  1. Article: Calcified Pilocytic Astrocytomas and Calcifying Pseudoneoplasms of the Neuraxis: A Diagnostic Challenge.

    Hernández-Reséndiz, Rebeca / Villanueva-Castro, Eliezer / Mateo-Nouel, Edgardo de Jesus / Gómez-Apo, Erick / Peñafiel-Salgado, Carlos / Salinas-Lara, Citlaltepetl / Tena-Suck, Martha Lilia

    Cureus

    2024  Volume 16, Issue 1, Page(s) e51765

    Abstract: Pilocytic astrocytoma (PA), recognized as the most prevalent central nervous system (CNS) tumor, has long been associated with calcifications, a characteristic often attributed to benign or indolent growth patterns. In this study, we explored the ... ...

    Abstract Pilocytic astrocytoma (PA), recognized as the most prevalent central nervous system (CNS) tumor, has long been associated with calcifications, a characteristic often attributed to benign or indolent growth patterns. In this study, we explored the calcified attributes in these tumors that beckon a deeper understanding. This is a retrospective study, on a set of seven cases, with a histopathological diagnosis of pilocytic astrocytoma with calcifications and psammoma bodies (PB). Despite an encouraging overall survival outcome, the recurrence in four cases cast some doubt on the conventional classification. The histological study of these cases revealed a spectrum of calcifications, varying in size and morphology, all of which exhibited positive reactivity to glial fibrillary acidic protein (GFAP), osteoconduction, and osteopontin. Notably, the immunohistochemistry showed hyaline bodies displaying an atypical immune profile, strikingly negative for vimentin and GFAP, and a robust positivity for epidermal growth factor receptors (EGFR), tumor necrosis factor-alpha (TNF-α), and interleukin 1 beta (IL-1β). These results stimulated speculation that the identity of these calcified tumors may have extended and potentially embraced the realm of calcifying pseudoneoplasms of the neuraxis (CAPNON), underscored by intense pilot gliosis. This study transcends mere anatomical exploration; it delves into the intricacies of calcified tumors, casting a spotlight on the dynamic interplay between PA and CAPNON. As we traverse the frontiers of neuro-oncology, these findings pave the way for innovative avenues in the diagnostics and therapeutics of these tumors.
    Language English
    Publishing date 2024-01-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2747273-5
    ISSN 2168-8184
    ISSN 2168-8184
    DOI 10.7759/cureus.51765
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article: Teratoma With Malignant Ectomesenchymoma in the Pineal Region: A Case Report.

    Hernández-Reséndiz, Rebeca / Villanueva-Castro, Eliezer / Chávez-Macías, Laura / Gómez-Apo, Erick / Ortiz-Plata, Alma / Salinas-Lara, Citlaltepetl / Peñafiel-Salgado, Carlos / Tena-Suck, Martha Lilia L

    Cureus

    2022  Volume 14, Issue 8, Page(s) e27711

    Abstract: Tumors involving the pineal gland include germinomas, non-germinomatous, and parenchymal tumors. Sometimes these tumors can be differentiated into rhabdomyosarcoma, which is an aggressive and rapidly recurring sarcoma but is a rare event. We present the ... ...

    Abstract Tumors involving the pineal gland include germinomas, non-germinomatous, and parenchymal tumors. Sometimes these tumors can be differentiated into rhabdomyosarcoma, which is an aggressive and rapidly recurring sarcoma but is a rare event. We present the case of a 23-year-old male, with an eight-year-long history of a non-treated brain tumor compatible with a teratoma. Chemotherapy and radiotherapy were offered, and two years later, malignant transformation to astrocytoma, rhabdomyosarcoma, neural cell carcinoma, ganglioglioma, and low-grade chondrosarcoma was noted. Immunohistochemistry was valuable in differentiating these entities that confirmed the diagnosis. Malignant transformations may be secondary to the normal transformation of multipotent embryonic cells into more developed tissues after radiotherapy of teratoma and malignant ectomesenchymoma transformation.
    Language English
    Publishing date 2022-08-05
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2747273-5
    ISSN 2168-8184
    ISSN 2168-8184
    DOI 10.7759/cureus.27711
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Mycobacterium tuberculosis

    Pérez-Noriega, Flaubert Alexis / Salinas-Lara, Citlaltepetl / Sánchez-Garibay, Carlos / Torres-Ruíz, José Jiram / Maravillas-Montero, José Luis / Castañón-Arreola, Mauricio / Hernández-Campos, María Elena / Rodríguez-Balderas, Cesar / Basurto-López, Beatriz Victoria / Peñafiel-Salgado, Carlos / Espinosa-García, Ana Paola / Choreño-Parra, José Alberto / Tena-Suck, Martha Lilia / Soto-Rojas, Luis O / León-Marroquín, Elsa Y / Romero-López, José Pablo / Castillejos-López, Manuel

    International journal of molecular sciences

    2023  Volume 24, Issue 2

    Abstract: Tuberculosis (TB) of the central nervous system (CNS) presents high mortality due to brain damage and inflammation events. The formation and deposition of immune complexes (ICs) in the brain microvasculature ... ...

    Abstract Tuberculosis (TB) of the central nervous system (CNS) presents high mortality due to brain damage and inflammation events. The formation and deposition of immune complexes (ICs) in the brain microvasculature during
    MeSH term(s) Male ; Animals ; Mice ; Mycobacterium tuberculosis ; Antigen-Antibody Complex ; Disease Models, Animal ; Tuberculosis/microbiology ; Antigens, Bacterial ; Vasculitis ; Cell Wall
    Chemical Substances Antigen-Antibody Complex ; Antigens, Bacterial
    Language English
    Publishing date 2023-01-08
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms24021242
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top