Inflammatory Myofibroblastic Tumor Presenting with Diabetes Insipidus in an Eight-Year-Old Boy: A Case Report |
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Authors: | Erkan Sar? Erman Ata? Engin Burak Bulut Sebahattin Sar? Onur Ak?n Mehmet Sald?r Y?ld?r?m Karsl?o?lu Ediz Ye?ilkaya |
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Affiliation: | 1. Gülhane Military Medicine Academy, Department of Pediatric Endocrinology, Ankara, Turkey ;2. Gülhane Military Medicine Academy, Department of Pediatric Oncology, Ankara, Turkey ;3. Gülhane Military Medicine Academy, Department of Pediatric Surgery, Ankara, Turkey ;4. Gülhane Military Medicine Academy, Department of Radiology, Ankara, Turkey ;5. Gülhane Military Medicine Academy, Department of Pathology, Ankara, Turkey |
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Abstract: | Inflammatory myofibroblastic tumors (IMT) develop as a non-neoplastic proliferation of myofibroblasts in a myxoid to collagenous stroma admixed with inflammatory cells. The symptoms depend on the specific location of the tumor, which can be anywhere, but is particularly in the respiratory system. Thus, patients with IMT can present with a variety of findings. A pediatric patient with IMT who presented with cough, breathlessness, polyuria-polydipsia, and convulsions is described in this report. |
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Keywords: | Inflammatory myofibroblastic tumor diabetes insipidus child |
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