Pleural fibrous tumor: case report
DOI:
https://doi.org/10.24054/cbs.v1i2.2636Keywords:
Primitive, Growth, Pleura, ExtrapleuralAbstract
The rare solitary fibroma of the pleura which has been studied to deepen the knowledge of its pathogenesis, diagnosis, and treatment, achieving excellent outcomes for the majority of patients affected by this pathology. In the two cases presented, the presence of immunohistochemical markers such as: CD34, STAT6, DESMINA, KI67 was evidenced in 5% and the solitary fibrous tumor was benign in 78% of the cases, as in the first case described in this article; Tumors with malignant behavior comprise 12% of this neoplasm, characterized by an indeterminate biological behavior, which can debut with weight loss, rapid growth, invasion of adjacent structures (lung, rib wall), pleural effusion, regional lymph node involvement, recurrence local and transfer as characteristic, despite the different nature of this type of tumors, surgical resection is the treatment of choice. Our objective is to describe the findings and outcomes of two patients surgically approached for the management of TFS, to make this a topic of high relevance in the academic and scientific community.
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