<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>51(12)</volume><submitter>Mitrovic-Jovanovic M</submitter><pubmed_abstract>Idiopathic mediastinal fibrosis, also called sclerosing or fibrosing mediastinitis, is a very rare and aggressive fibroinflammatory process characterized by fibrous tissue proliferation in the mediastinal region. Herein, we present a rare case of idiopathic mediastinal fibrosis presenting with esophageal obstruction, most likely associated with immunoglobulin G (IgG4)-related disease, affecting the posterior mediastinum with intrapulmonary infiltration. Computed tomography revealed a narrowed lumen and thickened wall of the distal esophagus surrounded by a necrotic mass with infiltration into the nearby structures, suggesting a locally advanced malignant process. Positron emission tomography revealed intense accumulation of 18F-fluorodeoxyglucose, indicating an active inflammatory component, which complicates further differential diagnosis of mediastinal masses. Thoracoscopic biopsy and immunohistochemical analysis confirmed a fibroinflammatory process with perivascular lymphoid cell infiltration that was cluster of differentiation (CD)3 (++) and CD20 (++), with massive numbers of IgG4-immunoreactive plasma cells. Although a benign condition, sclerosing mediastinitis is a close mimicker of esophageal carcinoma, which cannot be differentiated by computed tomography or positron emission tomography and must be considered in a differential diagnosis.</pubmed_abstract><journal>The Journal of international medical research</journal><pagination>3000605231213212</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10693803</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>CT and &lt;sup>18&lt;/sup>FDG-PET/CT findings in progressive mediastinal idiopathic fibrosis as a benign mimicker of esophageal carcinoma: a case report.</pubmed_title><pmcid>PMC10693803</pmcid><pubmed_authors>Djikic Rom A</pubmed_authors><pubmed_authors>Kostadinovic M</pubmed_authors><pubmed_authors>Simic A</pubmed_authors><pubmed_authors>Skrobic O</pubmed_authors><pubmed_authors>Plavsic A</pubmed_authors><pubmed_authors>Odalovic S</pubmed_authors><pubmed_authors>Jankovic A</pubmed_authors><pubmed_authors>Kovac JD</pubmed_authors><pubmed_authors>Mitrovic-Jovanovic M</pubmed_authors><pubmed_authors>Ivanovic N</pubmed_authors><pubmed_authors>Djuric-Stefanovic A</pubmed_authors></additional><is_claimable>false</is_claimable><name>CT and &lt;sup>18&lt;/sup>FDG-PET/CT findings in progressive mediastinal idiopathic fibrosis as a benign mimicker of esophageal carcinoma: a case report.</name><description>Idiopathic mediastinal fibrosis, also called sclerosing or fibrosing mediastinitis, is a very rare and aggressive fibroinflammatory process characterized by fibrous tissue proliferation in the mediastinal region. Herein, we present a rare case of idiopathic mediastinal fibrosis presenting with esophageal obstruction, most likely associated with immunoglobulin G (IgG4)-related disease, affecting the posterior mediastinum with intrapulmonary infiltration. Computed tomography revealed a narrowed lumen and thickened wall of the distal esophagus surrounded by a necrotic mass with infiltration into the nearby structures, suggesting a locally advanced malignant process. Positron emission tomography revealed intense accumulation of 18F-fluorodeoxyglucose, indicating an active inflammatory component, which complicates further differential diagnosis of mediastinal masses. Thoracoscopic biopsy and immunohistochemical analysis confirmed a fibroinflammatory process with perivascular lymphoid cell infiltration that was cluster of differentiation (CD)3 (++) and CD20 (++), with massive numbers of IgG4-immunoreactive plasma cells. Although a benign condition, sclerosing mediastinitis is a close mimicker of esophageal carcinoma, which cannot be differentiated by computed tomography or positron emission tomography and must be considered in a differential diagnosis.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2025-05-29T21:46:58.444Z</modification><creation>2025-05-29T21:46:58.444Z</creation></dates><accession>S-EPMC10693803</accession><cross_references><pubmed>38041832</pubmed><doi>10.1177/03000605231213212</doi></cross_references></HashMap>