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S M Tardio - One of the best experts on this subject based on the ideXlab platform.

  • a case of solitary fibrous Pleura Tumor associated with severe hypoglycemia the doege potter s syndrome
    Acta bio-medica : Atenei Parmensis, 2017
    Co-Authors: Silvia Haddoub, L Gnetti, A Montanari, R Di Ruvo, P Carbognani, F Maccanelli, M G Magotti, M C Calderini, Federico Cioni, S M Tardio
    Abstract:

    Solitary fibrous Pleura Tumor is a rare primary intrathoracic Tumor of the Pleura. It usually has an indolent clinical course, but sometimes it can have an aggressive behaviour. In 1930 Doege and Potter independently described this neoplasm, presenting with symptoms of hypoglycemia, hence the eponim of Doege-Potter’s Syndrome. In this report, we illustrate a case of Doege Potter’s Syndrome, treated with complete surgical resection.

Silvia Haddoub - One of the best experts on this subject based on the ideXlab platform.

  • a case of solitary fibrous Pleura Tumor associated with severe hypoglycemia the doege potter s syndrome
    Acta bio-medica : Atenei Parmensis, 2017
    Co-Authors: Silvia Haddoub, L Gnetti, A Montanari, R Di Ruvo, P Carbognani, F Maccanelli, M G Magotti, M C Calderini, Federico Cioni, S M Tardio
    Abstract:

    Solitary fibrous Pleura Tumor is a rare primary intrathoracic Tumor of the Pleura. It usually has an indolent clinical course, but sometimes it can have an aggressive behaviour. In 1930 Doege and Potter independently described this neoplasm, presenting with symptoms of hypoglycemia, hence the eponim of Doege-Potter’s Syndrome. In this report, we illustrate a case of Doege Potter’s Syndrome, treated with complete surgical resection.

Kyeong Cheol Shin - One of the best experts on this subject based on the ideXlab platform.

  • a case of solitary fibrous Pleura Tumor associated with severe hypoglycemia doege potter syndrome
    Tuberculosis and Respiratory Diseases, 2015
    Co-Authors: Jong Geol Jang, Kyung Soo Hong, Jae Ho Jo, Jin Hong Chung, Kyeong Cheol Shin
    Abstract:

    Solitary fibrous Tumor of the Pleura (SFTP) is a rare primary intrathoracic Tumor that arises from mesenchymal tissue underlying the mesothelial layer of the Pleura. It usually has an indolent clinical course. The hypoglycemia that accompanies SFTP was first described by Doege and Potter independently in 1930, hence the eponym Doege-Potter syndrome (DPS). The incidence of DPS is reported to be ~4%. In this report, we present a typical case of DPS that was cured through complete surgical resection.

R Di Ruvo - One of the best experts on this subject based on the ideXlab platform.

  • a case of solitary fibrous Pleura Tumor associated with severe hypoglycemia the doege potter s syndrome
    Acta bio-medica : Atenei Parmensis, 2017
    Co-Authors: Silvia Haddoub, L Gnetti, A Montanari, R Di Ruvo, P Carbognani, F Maccanelli, M G Magotti, M C Calderini, Federico Cioni, S M Tardio
    Abstract:

    Solitary fibrous Pleura Tumor is a rare primary intrathoracic Tumor of the Pleura. It usually has an indolent clinical course, but sometimes it can have an aggressive behaviour. In 1930 Doege and Potter independently described this neoplasm, presenting with symptoms of hypoglycemia, hence the eponim of Doege-Potter’s Syndrome. In this report, we illustrate a case of Doege Potter’s Syndrome, treated with complete surgical resection.

F Maccanelli - One of the best experts on this subject based on the ideXlab platform.

  • a case of solitary fibrous Pleura Tumor associated with severe hypoglycemia the doege potter s syndrome
    Acta bio-medica : Atenei Parmensis, 2017
    Co-Authors: Silvia Haddoub, L Gnetti, A Montanari, R Di Ruvo, P Carbognani, F Maccanelli, M G Magotti, M C Calderini, Federico Cioni, S M Tardio
    Abstract:

    Solitary fibrous Pleura Tumor is a rare primary intrathoracic Tumor of the Pleura. It usually has an indolent clinical course, but sometimes it can have an aggressive behaviour. In 1930 Doege and Potter independently described this neoplasm, presenting with symptoms of hypoglycemia, hence the eponim of Doege-Potter’s Syndrome. In this report, we illustrate a case of Doege Potter’s Syndrome, treated with complete surgical resection.