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EP.14C.08 Challenges in Diagnosis and Management of Epithelioid Inflammatory Myofibroblastic Sarcoma - Case Report
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The document outlines a medical case of a patient with EIMS (epithelioid inflammatory myofibroblastic sarcoma), a rare and aggressive cancer. Initially diagnosed in December 2018 following a right upper lobectomy, histology confirmed the presence of EIMS with ALK expression.<br /><br />By March 2020, the disease had progressed to the brain, with persistent headaches and double vision indicating metastasis. A significant metastatic tumor was found in the right frontoparietal region, requiring surgical removal and subsequent anticonvulsant and corticosteroid therapy.<br /><br />In May 2020, further disease progression was noted, with multiple brain lesions detected in follow-up CT scans. The patient was considered for external radiotherapy, which commenced as they awaited approval for Anaplastic Lymphoma Kinase Tyrosine Kinase Inhibitor (ALK-TKI) treatment. Targeted therapy with alectinib began in June 2020, allowing for the discontinuation of radiotherapy.<br /><br />In May 2021, a new tumor was discovered and surgically excised, which was diagnosed as a fibrous meningioma. Further disease progression occurred by June 2023, accompanied by another seizure and a CT scan revealing a high tumor in the right frontal region, necessitating additional neurosurgery.<br /><br />Overall, the patient's treatment course highlights the complexities in managing EIMS, with challenges arising from tumor recurrence and metastasis, necessitating a combination of surgical, radiotherapeutic, and targeted therapies.
Asset Subtitle
Michal Urda
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Speaker
Michal Urda
Topic
Mesothelioma, Thymoma, and Other Thoracic Tumors
Keywords
EIMS
epithelioid inflammatory myofibroblastic sarcoma
ALK expression
brain metastasis
surgical removal
anticonvulsant therapy
corticosteroid therapy
ALK-TKI treatment
alectinib
tumor recurrence
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